Anticandidal Activity and Mechanism of Action of Several Cationic Chimeric Antimicrobial Peptides

Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity...

Full description

Saved in:
Bibliographic Details
Published inInternational journal of peptide research and therapeutics Vol. 29; no. 3; p. 50
Main Authors Memariani, Mojtaba, Memariani, Hamed, Moravvej, Hamideh, Goudarzi, Hossein, Robati, Reza Mahmoud
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 06.05.2023
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity and mechanism of action of previously designed cationic chimeric AMPs, namely PV, BVP, PVP, and PV3. These four AMPs had a high tendency to adopt alpha-helical conformation based upon peptide structure prediction and circular dichroism. The geometric mean minimum inhibitory concentration (GMMIC) values (and ranges) of PV, BVP, PVP, and PV3 for all Candida albicans isolates (in µg/mL) were 1.83 (1–2), 93.33 (16 to >128), 3.25 (0.5–8), and 1.42 (0.5–2), respectively. At ≥ 8 µg/mL, all of the AMPs dose-dependently reduced in vitro viability of human fibroblast cells, with PV being the most cytotoxic peptide. Among the tested peptides, PV3 exhibited the highest cell selectivity index (determined as the ratio of CC 50 to GMMIC). Rapid candidacidal kinetics, disruption of cell wall/membrane integrity, and inhibition of yeast-to-hypha morphological switch were other important properties of the tested AMPs. Atomic force microscopy revealed that PV3 was able to induce major morpho-structural deformities in yeast cells such as blebs, cell shrinkage, and holes. Based on Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy analysis, the polysaccharide content of the yeast cells was increased markedly in response to sub-lethal doses of PV3. Despite these encouraging data, much remains to be learned about in vivo efficacy and safety of these AMPs.
AbstractList Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity and mechanism of action of previously designed cationic chimeric AMPs, namely PV, BVP, PVP, and PV3. These four AMPs had a high tendency to adopt alpha-helical conformation based upon peptide structure prediction and circular dichroism. The geometric mean minimum inhibitory concentration (GMMIC) values (and ranges) of PV, BVP, PVP, and PV3 for all Candida albicans isolates (in µg/mL) were 1.83 (1–2), 93.33 (16 to >128), 3.25 (0.5–8), and 1.42 (0.5–2), respectively. At ≥ 8 µg/mL, all of the AMPs dose-dependently reduced in vitro viability of human fibroblast cells, with PV being the most cytotoxic peptide. Among the tested peptides, PV3 exhibited the highest cell selectivity index (determined as the ratio of CC50 to GMMIC). Rapid candidacidal kinetics, disruption of cell wall/membrane integrity, and inhibition of yeast-to-hypha morphological switch were other important properties of the tested AMPs. Atomic force microscopy revealed that PV3 was able to induce major morpho-structural deformities in yeast cells such as blebs, cell shrinkage, and holes. Based on Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy analysis, the polysaccharide content of the yeast cells was increased markedly in response to sub-lethal doses of PV3. Despite these encouraging data, much remains to be learned about in vivo efficacy and safety of these AMPs.
Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity and mechanism of action of previously designed cationic chimeric AMPs, namely PV, BVP, PVP, and PV3. These four AMPs had a high tendency to adopt alpha-helical conformation based upon peptide structure prediction and circular dichroism. The geometric mean minimum inhibitory concentration (GMMIC) values (and ranges) of PV, BVP, PVP, and PV3 for all Candida albicans isolates (in µg/mL) were 1.83 (1–2), 93.33 (16 to >128), 3.25 (0.5–8), and 1.42 (0.5–2), respectively. At ≥ 8 µg/mL, all of the AMPs dose-dependently reduced in vitro viability of human fibroblast cells, with PV being the most cytotoxic peptide. Among the tested peptides, PV3 exhibited the highest cell selectivity index (determined as the ratio of CC 50 to GMMIC). Rapid candidacidal kinetics, disruption of cell wall/membrane integrity, and inhibition of yeast-to-hypha morphological switch were other important properties of the tested AMPs. Atomic force microscopy revealed that PV3 was able to induce major morpho-structural deformities in yeast cells such as blebs, cell shrinkage, and holes. Based on Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy analysis, the polysaccharide content of the yeast cells was increased markedly in response to sub-lethal doses of PV3. Despite these encouraging data, much remains to be learned about in vivo efficacy and safety of these AMPs.
ArticleNumber 50
Author Memariani, Hamed
Moravvej, Hamideh
Goudarzi, Hossein
Memariani, Mojtaba
Robati, Reza Mahmoud
Author_xml – sequence: 1
  givenname: Mojtaba
  orcidid: 0000-0002-4964-3117
  surname: Memariani
  fullname: Memariani, Mojtaba
  organization: Skin Research Center, Shahid Beheshti University of Medical Sciences
– sequence: 2
  givenname: Hamed
  orcidid: 0000-0003-1026-140X
  surname: Memariani
  fullname: Memariani, Hamed
  email: h.memariani@gmail.com
  organization: Skin Research Center, Shahid Beheshti University of Medical Sciences
– sequence: 3
  givenname: Hamideh
  orcidid: 0000-0002-9425-7282
  surname: Moravvej
  fullname: Moravvej, Hamideh
  email: hamideh_moravvej@yahoo.com, hamidehmoravej@sbmu.ac.ir
  organization: Skin Research Center, Shahid Beheshti University of Medical Sciences
– sequence: 4
  givenname: Hossein
  surname: Goudarzi
  fullname: Goudarzi, Hossein
  organization: Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences
– sequence: 5
  givenname: Reza Mahmoud
  orcidid: 0000-0002-7947-8642
  surname: Robati
  fullname: Robati, Reza Mahmoud
  organization: Skin Research Center, Shahid Beheshti University of Medical Sciences
BookMark eNp9kF1LwzAUhoNMcFP_gFcFr6snH22ay1H8gomCeh3SNHUZazuTbLB_b7oKihe7yss573POyTtDk67vDEJXGG4wAL_1GEQhUiA0xZCRLCUnaIozTlMqgE3-6DM0834F0cQxTJGad8Fq1dW2VutkroPd2bBPYiF5NnqpOuvbpG8Onb4b1JvZGRe9pRoqVifl0rbGRTGMaq12fWVj_9Vsgq2Nv0CnjVp7c_nznqOP-7v38jFdvDw8lfNFqikWITWcsYwKzRtc4IaDYBoYqwEanNOai4qBymuqSU4LAZoaXDFjKMu1YqrKK3qOrse5G9d_bY0PctVvXRdXSlJgIBlwTKOLjK54pvfONHLjbKvcXmKQQ5RyjFLGKOUhSkkiVPyDtA2H7wen7Po4SkfUxz3dp3G_Vx2hvgE094oO
CitedBy_id crossref_primary_10_1007_s11274_023_03852_5
crossref_primary_10_1111_imb_12934
Cites_doi 10.1007/s10989-022-10401-5
10.3390/ijms20225713
10.1586/eri.11.152
10.1016/bs.podrm.2020.07.005
10.1042/BJ20111454
10.1371/journal.pone.0180680
10.1002/psc.2827
10.3390/ijms21061912
10.1038/s41598-021-00223-8
10.1007/s11274-023-03545
10.1016/j.resmic.2010.11.006
10.1016/j.bbamem.2017.06.005
10.4155/fmc-2020-0052
10.1038/s41467-022-32249-5
10.1007/s00253-020-10701-0
10.3390/life12101581
10.1038/s41467-018-03746-3
10.1007/s12010-021-03553-5
10.3390/antibiotics9080454
10.1002/bip.360360611
10.3390/jof9020171
10.1128/EC.05030-11
10.3390/md20080501
10.1038/nmeth.3213
10.1038/ja.2013.140
10.1128/AAC.00190-16
10.1007/s00726-020-02903-7
10.1128/AAC.48.2.369-377.2004
10.1007/s40475-021-00226-5
10.1007/s00216-009-3316-5
10.1016/j.gene.2018.05.106
10.3389/fcimb.2020.00105
10.1111/cmi.13093
10.1038/nrd.2017.46
10.1016/j.bbrc.2016.09.045
10.1371/journal.pntd.0009092
10.1007/s12602-020-09685-0
10.1128/AAC.49.4.1340-1345.2005
10.1038/nprot.2010.5
10.1080/21505594.2021.2019950
10.3390/jof8101018
10.3390/pathogens10070859
10.1016/j.colsurfb.2016.02.003
10.1007/s10989-014-9430-z
10.1248/bpb.27.751
10.1155/2021/5597758
10.1016/j.chom.2022.10.004
10.1038/srep27258
10.1002/med.21542
10.1111/j.1399-3011.1996.tb00809.x
10.3389/fcimb.2017.00249
10.1021/acsinfecdis.0c00356
10.1038/srep09657
10.1038/nmicrobiol.2016.162
10.1007/s10989-018-9739-0
10.3390/ijms24021584
10.3390/jof5010021
10.1038/nrmicro.2016.157
10.1111/cbdd.12864
10.1016/j.toxicon.2013.08.056
10.1016/j.peptides.2011.06.003
10.1186/1471-2180-13-246
10.1007/s00726-012-1305-z
10.1016/j.biochi.2016.05.013
10.1038/s41598-020-67041-2
10.5772/intechopen.99737
ContentType Journal Article
Copyright The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
Copyright_xml – notice: The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
DBID AAYXX
CITATION
3V.
7X7
7XB
88A
88I
8AO
8FE
8FH
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0S
M2P
M7P
PHGZM
PHGZT
PKEHL
PQEST
PQGLB
PQQKQ
PQUKI
Q9U
DOI 10.1007/s10989-023-10525-2
DatabaseName CrossRef
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Biology Database (Alumni Edition)
Science Database (Alumni Edition)
ProQuest Pharma Collection
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
Biological Sciences
ProQuest Health & Medical Collection
Science Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central Basic
DatabaseTitle CrossRef
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Biology Journals (Alumni Edition)
ProQuest Central
ProQuest One Applied & Life Sciences
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Biological Science Collection
ProQuest Central (New)
ProQuest Science Journals (Alumni Edition)
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest Science Journals
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest Central (Alumni)
ProQuest One Academic (New)
DatabaseTitleList ProQuest Central Student

Database_xml – sequence: 1
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
Chemistry
EISSN 1573-3904
ExternalDocumentID 10_1007_s10989_023_10525_2
GroupedDBID ---
-56
-5G
-BR
-EM
-~C
.86
.VR
06C
06D
0R~
0VY
203
29J
29~
2J2
2JN
2JY
2KG
2KM
2LR
2~H
30V
4.4
406
408
409
40E
53G
5GY
67N
67Z
6NX
7X7
88I
8AO
8CJ
8FE
8FH
8FI
8FJ
8TC
8UJ
95-
95.
95~
96X
AAAVM
AABHQ
AACDK
AAHNG
AAIAL
AAJBT
AAJKR
AANZL
AARTL
AASML
AATNV
AATVU
AAUYE
AAWCG
AAYIU
AAYQN
AAYZH
ABAKF
ABBBX
ABBXA
ABDBF
ABDZT
ABECU
ABFTV
ABHLI
ABHQN
ABJNI
ABJOX
ABKCH
ABKTR
ABMNI
ABMQK
ABNWP
ABPLI
ABQBU
ABSXP
ABTEG
ABTHY
ABTKH
ABTMW
ABUWG
ABWNU
ABXPI
ACAOD
ACDTI
ACGFS
ACGOD
ACHSB
ACHXU
ACKNC
ACMDZ
ACMLO
ACOKC
ACOMO
ACPIV
ACPRK
ACSNA
ACUHS
ACZOJ
ADBBV
ADHIR
ADINQ
ADKNI
ADRFC
ADTPH
ADURQ
ADYFF
ADZKW
AEFQL
AEGAL
AEGNC
AEJHL
AEJRE
AEMSY
AENEX
AEOHA
AEPYU
AESKC
AETLH
AEVLU
AEXYK
AFBBN
AFKRA
AFLOW
AFQWF
AFWTZ
AFZKB
AGAYW
AGDGC
AGMZJ
AGQEE
AGQMX
AGRTI
AGWIL
AGWZB
AGYKE
AHAVH
AHBYD
AHMBA
AHSBF
AHYZX
AIAKS
AIGIU
AIIXL
AILAN
AITGF
AJRNO
AJZVZ
AKMHD
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALWAN
AMKLP
AMXSW
AMYLF
AOCGG
ARMRJ
ASPBG
AVWKF
AXYYD
AZFZN
AZQEC
B-.
BA0
BBNVY
BENPR
BGNMA
BHPHI
BPHCQ
BSONS
BVXVI
CCPQU
CS3
CSCUP
D1J
DDRTE
DL5
DNIVK
DPUIP
DU5
DWQXO
EBD
EBLON
EBS
EIOEI
EPAXT
ESBYG
F5P
FEDTE
FERAY
FFXSO
FIGPU
FNLPD
FRRFC
FWDCC
FYUFA
G-Y
G-Z
GGCAI
GGRSB
GJIRD
GNUQQ
GNWQR
GQ6
GQ7
GQ8
GXS
HCIFZ
HF~
HG5
HG6
HMCUK
HMJXF
HQYDN
HRMNR
HVGLF
I09
IJ-
IKXTQ
IWAJR
IXC
IXD
IXE
IZIGR
IZQ
I~X
I~Z
J-C
J0Z
JBSCW
JCJTX
JZLTJ
KDC
KOV
KPH
LK8
LLZTM
M2P
M4Y
M7P
MA-
NB0
NPVJJ
NQJWS
NU0
O93
O9G
O9I
O9J
OAM
P19
PF0
PQQKQ
PROAC
PT4
PT5
Q2X
QOR
QOS
R89
R9I
RNS
ROL
RPX
RSV
S16
S27
S3A
S3B
SAP
SBL
SDH
SHX
SISQX
SJYHP
SNE
SNPRN
SNX
SOHCF
SOJ
SPISZ
SRMVM
SSLCW
SSXJD
STPWE
SZN
T13
TSG
TSK
TSV
TUC
U2A
U9L
UG4
UKHRP
UOJIU
UTJUX
VC2
W23
W48
WJK
WK8
YLTOR
Z45
Z7U
Z87
Z8O
Z91
ZMTXR
ZOVNA
~A9
AAPKM
AAYXX
ABBRH
ABDBE
ABFSG
ACSTC
AEZWR
AFDZB
AFHIU
AFOHR
AHPBZ
AHWEU
AIXLP
ATHPR
AYFIA
CITATION
PHGZM
PHGZT
3V.
7XB
88A
8FK
ABRTQ
K9.
PKEHL
PQEST
PQGLB
PQUKI
Q9U
ID FETCH-LOGICAL-c319t-e744539c7f181f7094c044d00f163d79b40a6d3c263890c3e1b4ee346ca4ab6b3
IEDL.DBID 7X7
ISSN 1573-3904
1573-3149
IngestDate Fri Jul 25 18:56:45 EDT 2025
Thu Apr 24 23:13:32 EDT 2025
Tue Jul 01 02:21:38 EDT 2025
Fri Feb 21 02:43:22 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords Hyphal transition
Cytotoxicity
Membrane integrity
Antimicrobial peptides
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c319t-e744539c7f181f7094c044d00f163d79b40a6d3c263890c3e1b4ee346ca4ab6b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ORCID 0000-0002-7947-8642
0000-0002-4964-3117
0000-0003-1026-140X
0000-0002-9425-7282
PQID 2810250713
PQPubID 54427
ParticipantIDs proquest_journals_2810250713
crossref_primary_10_1007_s10989_023_10525_2
crossref_citationtrail_10_1007_s10989_023_10525_2
springer_journals_10_1007_s10989_023_10525_2
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2023-05-06
PublicationDateYYYYMMDD 2023-05-06
PublicationDate_xml – month: 05
  year: 2023
  text: 2023-05-06
  day: 06
PublicationDecade 2020
PublicationPlace Dordrecht
PublicationPlace_xml – name: Dordrecht
PublicationSubtitle formerly known as "Letters in Peptide Science"
PublicationTitle International journal of peptide research and therapeutics
PublicationTitleAbbrev Int J Pept Res Ther
PublicationYear 2023
Publisher Springer Netherlands
Springer Nature B.V
Publisher_xml – name: Springer Netherlands
– name: Springer Nature B.V
References Yang, Yan, Roy, Xu, Poisson, Zhang (CR68) 2015; 12
Perfect (CR46) 2017; 16
Wang, Dou, Song, Lyu, Zhu, Xu, Li, Shan (CR65) 2019; 39
Bohner, Gacser, Toth (CR5) 2021; 8
Memariani, Memariani (CR30) 2020; 104
Lopes, Lionakis (CR25) 2022; 13
Memariani, Shahbazzadeh, Sabatier, Memariani, Karbalaeimahdi, Bagheri (CR32) 2016; 479
Acar, Pelit Arayıcı, Ucar, Karahan, Mustafaeva (CR1) 2019; 25
Fernández de Ullivarri, Arbulu, Garcia-Gutierrez, Cotter (CR12) 2020; 10
Saucedo-Vázquez, Gushque, Vispo, Rodriguez, Gudiño-Gomezjurado, Albericio, Tellkamp, Alexis (CR55) 2022; 20
Santamaría, Larios, Quirós, Pizarro-Cerda, Gorvel, Lomonte, Moreno (CR53) 2005; 49
Smart, Mason, Bennell, Maeij, Geysen (CR58) 1996; 47
Roy, Kucukural, Zhang (CR51) 2010; 5
Chow, Pang, Wang (CR8) 2021; 10
Kodedová, Sychrová (CR20) 2017; 1859
Kim, Park, Noh, Kim, Yoo, Kim, Lee, Jang (CR19) 2020; 9
Lam, O'Brien-Simpson, Pantarat, Sulistio, Wong, Chen, Lenzo, Holden, Blencowe, Reynolds, Qiao (CR24) 2016; 1
Sato, Watanabe, Mikami, Matsumoto (CR54) 2004; 27
Sowa-Jasiłek, Zdybicka-Barabas, Stączek, Pawlikowska-Pawlęga, Grygorczuk-Płaneta, Skrzypiec, Gruszecki, Mak, Cytryńska (CR59) 2020; 21
CR9
Yang, Wang, Lee, Zhang (CR67) 2013; 74
Garvey, Rowan (CR13) 2023; 24
Jacobsen, Wilson, Wächtler, Brunke, Naglik, Hube (CR18) 2012; 10
Wade, Lin, Hossain, Dawson (CR64) 2012; 43
Memariani, Memariani, Poursafavi, Baseri (CR34) 2022; 28
CR44
Gow, Johnson, Berman, Coste, Cuomo, Perlin, Bicanic, Harrison, Wiederhold, Bromley, Chiller, Edgar (CR15) 2022; 13
Chotigavin, Sriphochanart, Yaiyen, Kudan (CR7) 2021; 193
Moravvej, Memariani, Memariani, Kabir-Salmani, Shoae-Hassani, Abdollahimajd (CR37) 2021; 2021
Shareck, Belhumeur (CR57) 2011; 10
Maurya, Pathak, Sharma, Sanwal, Chaudhary, Tupe, Deshpande, Chauhan, Prasad (CR29) 2011; 32
Kodedová, Valachovič, Csáky, Sychrová (CR21) 2019; 21
Vanreppelen, Wuyts, Van Dijck, Vandecruys (CR63) 2023; 9
Nam, Choi, Kumar, Nielsen, Kyeong, Wang, Kang, Lee, Lee, Yoon, Hong, Lund, Jenssen, Shin, Seo (CR39) 2020; 10
Stepanov, Poshvina, Vasilchenko (CR60) 2022; 8
Lum, Tay, Le, Lee, Sabri, Velayuthan, Hassan, Sekaran (CR26) 2015; 5
Noble, Gianetti, Witchley (CR42) 2017; 15
Naruemon, Romanee, Cheunjit, Xiao, McLandsborough, Pawadee (CR41) 2013; 20
Nargesi, Bongomin, Hedayati (CR40) 2021; 15
Indrayanto, Putra, Suhud (CR17) 2021; 46
Park, Yamato, Lee, Sugihara (CR43) 1995; 36
CR10
Tsang, Wong, Jung, Fong (CR62) 2014; 67
Martin, Kavanagh, Velasco-Torrijos (CR28) 2021; 13
Peng, Liu, Shui, Zhao, Mao, Liu (CR45) 2022; 12
Saulou, Jamme, Maranges, Fourquaux, Despax, Raynaud, Dumas, Mercier-Bonin (CR56) 2010; 396
Porto, Irazazabal, Alves, Ribeiro, Matos, Pires, Fensterseifer, Miranda, Haney, Humblot, Torres, Hancock, Liao, Ladram, Lu, de la Fuente-Nunez, Franco (CR47) 2018; 9
Memariani, Memariani (CR31) 2023; 39
Chang, Tsai, Huang, Liu, Chien, Lan (CR6) 2012; 441
Wanmakok, Orrapin, Intorasoot, Intorasoot (CR66) 2018; 671
Bacalum, Radu (CR2) 2015; 21
Hollmann, Martínez, Noguera, Augusto, Disalvo, Santos, Semorile, Maffía (CR16) 2016; 141
Samot, Rouabhia (CR52) 2021; 13
Bakare, Keyster, Pretorius (CR3) 2021; 11
Rautenbach, Troskie, Vosloo (CR48) 2016; 130
Faya, Hazzah, Omolo, Agrawal, Maji, Walvekar, Mocktar, Nkambule, Rambharose, Albericio, de la Torre, Govender (CR11) 2020; 52
Kornitzer (CR22) 2019; 5
Theberge, Semlali, Alamri, Leung, Rouabhia (CR61) 2013; 13
Reen, Phelan, Gallagher, Woods, Shanahan, Cano, ÓMuimhneacháin, McGlacken, O'Gara (CR49) 2016; 60
Mueller, de la Pena, Derendorf (CR38) 2004; 48
Lyu, Yang, Lyu, Dong, Shan (CR27) 2016; 6
Mihoubi, Sahli, Gargouri, Amiel (CR35) 2017; 12
Mora-Navarro, Caraballo-León, Torres-Lugo, Ortiz-Bermúdez (CR36) 2015; 21
Rončević, Puizina, Tossi (CR50) 2019; 20
Basso, Dang, Urisman, Cowen, Madhani, Noble (CR4) 2022; 30
Memariani, Shahbazzadeh, Ranjbar, Behdani, Memariani, Pooshang Bagheri (CR33) 2017; 89
Gonçalves, Silva, Felício, de Medeiros, Kurtenbach, Santos (CR14) 2017; 7
La Storia, Ercolini, Marinello, Di Pasqua, Villani, Mauriello (CR23) 2011; 162
NA Gow (10525_CR15) 2022; 13
SS Smart (10525_CR58) 1996; 47
P Basso (10525_CR4) 2022; 30
SJ Lam (10525_CR24) 2016; 1
S Nargesi (10525_CR40) 2021; 15
EW Chow (10525_CR8) 2021; 10
M Faya (10525_CR11) 2020; 52
T Rončević (10525_CR50) 2019; 20
ID Jacobsen (10525_CR18) 2012; 10
M Kodedová (10525_CR21) 2019; 21
J Wang (10525_CR65) 2019; 39
PW Tsang (10525_CR62) 2014; 67
Y Lyu (10525_CR27) 2016; 6
X Yang (10525_CR67) 2013; 74
M Bacalum (10525_CR2) 2015; 21
J Shareck (10525_CR57) 2011; 10
M Garvey (10525_CR13) 2023; 24
S Theberge (10525_CR61) 2013; 13
C Mora-Navarro (10525_CR36) 2015; 21
KY Lum (10525_CR26) 2015; 5
H Memariani (10525_CR33) 2017; 89
OO Bakare (10525_CR3) 2021; 11
H Moravvej (10525_CR37) 2021; 2021
WF Porto (10525_CR47) 2018; 9
10525_CR44
F Bohner (10525_CR5) 2021; 8
S Gonçalves (10525_CR14) 2017; 7
C Saulou (10525_CR56) 2010; 396
M Rautenbach (10525_CR48) 2016; 130
SM Noble (10525_CR42) 2017; 15
C Santamaría (10525_CR53) 2005; 49
AA Stepanov (10525_CR60) 2022; 8
10525_CR9
IK Maurya (10525_CR29) 2011; 32
M Mueller (10525_CR38) 2004; 48
M Memariani (10525_CR34) 2022; 28
JD Wade (10525_CR64) 2012; 43
HT Chang (10525_CR6) 2012; 441
JR Perfect (10525_CR46) 2017; 16
J Samot (10525_CR52) 2021; 13
H Memariani (10525_CR32) 2016; 479
10525_CR10
M Naruemon (10525_CR41) 2013; 20
NG Park (10525_CR43) 1995; 36
JY Kim (10525_CR19) 2020; 9
M Kodedová (10525_CR20) 2017; 1859
C Peng (10525_CR45) 2022; 12
G Indrayanto (10525_CR17) 2021; 46
H Memariani (10525_CR30) 2020; 104
A La Storia (10525_CR23) 2011; 162
FJ Reen (10525_CR49) 2016; 60
D Kornitzer (10525_CR22) 2019; 5
T Sato (10525_CR54) 2004; 27
J Yang (10525_CR68) 2015; 12
A Roy (10525_CR51) 2010; 5
G Vanreppelen (10525_CR63) 2023; 9
JP Saucedo-Vázquez (10525_CR55) 2022; 20
JP Lopes (10525_CR25) 2022; 13
H Martin (10525_CR28) 2021; 13
M Wanmakok (10525_CR66) 2018; 671
HY Nam (10525_CR39) 2020; 10
H Memariani (10525_CR31) 2023; 39
W Mihoubi (10525_CR35) 2017; 12
N Chotigavin (10525_CR7) 2021; 193
A Hollmann (10525_CR16) 2016; 141
T Acar (10525_CR1) 2019; 25
M Fernández de Ullivarri (10525_CR12) 2020; 10
A Sowa-Jasiłek (10525_CR59) 2020; 21
References_xml – volume: 28
  start-page: 96
  year: 2022
  ident: CR34
  article-title: Anti-fungal effects and mechanisms of action of wasp venom-derived peptide mastoparan-VT1 against
  publication-title: Int J Pept Res Ther
  doi: 10.1007/s10989-022-10401-5
– volume: 20
  start-page: 5713
  year: 2019
  ident: CR50
  article-title: Antimicrobial peptides as antiinfective agents in pre-post-antibiotic era?
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms20225713
– volume: 10
  start-page: 85
  issue: 1
  year: 2012
  end-page: 93
  ident: CR18
  article-title: dimorphism as a therapeutic target
  publication-title: Expert Rev Anti Infect Ther
  doi: 10.1586/eri.11.152
– volume: 46
  start-page: 273
  year: 2021
  end-page: 307
  ident: CR17
  article-title: Validation of in-vitro bioassay methods: application in herbal drug research
  publication-title: Profiles Drug Subst Excip Relat Methodol
  doi: 10.1016/bs.podrm.2020.07.005
– volume: 441
  start-page: 963
  issue: 3
  year: 2012
  end-page: 970
  ident: CR6
  article-title: LL37 and hBD-3 elevate the β-1, 3-exoglucanase activity of Xog1p, resulting in reduced fungal adhesion to plastic
  publication-title: Biochem J
  doi: 10.1042/BJ20111454
– volume: 12
  start-page: e0180680
  issue: 7
  year: 2017
  ident: CR35
  article-title: FTIR spectroscopy of whole cells for the monitoring of yeast apoptosis mediated by p53 over-expression and its suppression by extracts
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0180680
– volume: 21
  start-page: 853
  issue: 12
  year: 2015
  end-page: 861
  ident: CR36
  article-title: Synthetic antimicrobial β-peptide in dual-treatment with fluconazole or ketoconazole enhances the in vitro inhibition of planktonic and biofilm
  publication-title: J Pept Sci
  doi: 10.1002/psc.2827
– volume: 21
  start-page: 1912
  year: 2020
  ident: CR59
  article-title: Antifungal activity of anionic defense peptides: insight into the action of anionic peptide 2
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms21061912
– volume: 11
  start-page: 20621
  issue: 1
  year: 2021
  ident: CR3
  article-title: Building HMM and molecular docking analysis for the sensitive detection of anti-viral pneumonia antimicrobial peptides (AMPs)
  publication-title: Sci Rep
  doi: 10.1038/s41598-021-00223-8
– volume: 39
  start-page: 99
  issue: 4
  year: 2023
  ident: CR31
  article-title: Antibiofilm properties of cathelicidin LL-37: an in-depth review
  publication-title: World J Microbiol Biotechnol
  doi: 10.1007/s11274-023-03545
– volume: 162
  start-page: 164
  year: 2011
  end-page: 172
  ident: CR23
  article-title: Atomic force microscopy analysis shows surface structure changes in carvacrol-treated bacterial cells
  publication-title: Res Microbiol
  doi: 10.1016/j.resmic.2010.11.006
– volume: 1859
  start-page: 1851
  year: 2017
  end-page: 1858
  ident: CR20
  article-title: Synthetic antimicrobial peptides of the halictines family disturb the membrane integrity of cells
  publication-title: Biochim Biophys Acta Biomembr
  doi: 10.1016/j.bbamem.2017.06.005
– volume: 13
  start-page: 313
  year: 2021
  end-page: 334
  ident: CR28
  article-title: Targeting adhesion in fungal pathogen
  publication-title: Future Med Chem
  doi: 10.4155/fmc-2020-0052
– volume: 13
  start-page: 5352
  issue: 1
  year: 2022
  ident: CR15
  article-title: The importance of antimicrobial resistance in medical mycology
  publication-title: Nat Commun
  doi: 10.1038/s41467-022-32249-5
– volume: 104
  start-page: 6513
  year: 2020
  end-page: 6526
  ident: CR30
  article-title: Anti-fungal properties and mechanisms of melittin
  publication-title: Appl Microbiol Biotechnol
  doi: 10.1007/s00253-020-10701-0
– volume: 12
  start-page: 1581
  issue: 10
  year: 2022
  ident: CR45
  article-title: Mechanisms of action of the antimicrobial peptide cecropin in the killing of
  publication-title: Life (basel)
  doi: 10.3390/life12101581
– volume: 9
  start-page: 1490
  issue: 1
  year: 2018
  ident: CR47
  article-title: In silico optimization of aguava antimicrobial peptide enables combinatorial exploration for peptide design
  publication-title: Nat Commun
  doi: 10.1038/s41467-018-03746-3
– volume: 193
  start-page: 2591
  issue: 8
  year: 2021
  end-page: 2601
  ident: CR7
  article-title: Increasing the production of β-glucan from RU01 by using tannic acid
  publication-title: Appl Biochem Biotechnol
  doi: 10.1007/s12010-021-03553-5
– volume: 9
  start-page: 454
  issue: 8
  year: 2020
  ident: CR19
  article-title: Antifungal effect of a chimeric peptide Hn-Mc against pathogenic fungal strains
  publication-title: Antibiotics
  doi: 10.3390/antibiotics9080454
– volume: 36
  start-page: 793
  issue: 6
  year: 1995
  end-page: 801
  ident: CR43
  article-title: Interaction of mastoparan-B from venom of a hornet in Taiwan with phospholipid bilayers and its antimicrobial activity
  publication-title: Biopolymers
  doi: 10.1002/bip.360360611
– volume: 9
  start-page: 171
  issue: 2
  year: 2023
  ident: CR63
  article-title: Sources of antifungal drugs
  publication-title: J Fungi
  doi: 10.3390/jof9020171
– ident: CR9
– volume: 10
  start-page: 1004
  issue: 8
  year: 2011
  end-page: 1012
  ident: CR57
  article-title: Modulation of morphogenesis in by various small molecules
  publication-title: Eukaryot Cell
  doi: 10.1128/EC.05030-11
– volume: 20
  start-page: 501
  issue: 8
  year: 2022
  ident: CR55
  article-title: Marine Arthropods as a source of antimicrobial peptides
  publication-title: Mar Drugs
  doi: 10.3390/md20080501
– volume: 12
  start-page: 7
  issue: 1
  year: 2015
  end-page: 8
  ident: CR68
  article-title: The I-TASSER Suite: protein structure and function prediction
  publication-title: Nat Methods
  doi: 10.1038/nmeth.3213
– volume: 67
  start-page: 349
  issue: 4
  year: 2014
  end-page: 350
  ident: CR62
  article-title: Sub-MIC levels of purpurin inhibit membrane ATPase-mediated proton efflux activity in the human fungal pathogen
  publication-title: J Antibiot (tokyo)
  doi: 10.1038/ja.2013.140
– volume: 60
  start-page: 5894
  issue: 10
  year: 2016
  end-page: 5905
  ident: CR49
  article-title: Exploiting interkingdom interactions for development of small-molecule inhibitors of biofilm formation
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.00190-16
– volume: 52
  start-page: 1439
  year: 2020
  end-page: 1457
  ident: CR11
  article-title: Novel formulation of antimicrobial peptides enhances antimicrobial activity against methicillin-resistant (MRSA)
  publication-title: Amino Acids
  doi: 10.1007/s00726-020-02903-7
– volume: 48
  start-page: 369
  year: 2004
  end-page: 377
  ident: CR38
  article-title: Issues in pharmacokinetics and pharmacodynamics of anti-infective agents: kill curves versus MIC
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.48.2.369-377.2004
– volume: 8
  start-page: 59
  year: 2021
  end-page: 68
  ident: CR5
  article-title: Epidemiological attributes of species in tropical regions
  publication-title: Curr Trop Med Rep
  doi: 10.1007/s40475-021-00226-5
– volume: 396
  start-page: 1441
  year: 2010
  end-page: 1450
  ident: CR56
  article-title: Synchrotron FTIR microspectroscopy of the yeast after exposure to plasma-deposited nanosilver-containing coating
  publication-title: Anal Bioanal Chem
  doi: 10.1007/s00216-009-3316-5
– volume: 671
  start-page: 1
  year: 2018
  end-page: 9
  ident: CR66
  article-title: Expression in of novel recombinant hybrid antimicrobial peptide AL32-P113 with enhanced antimicrobial activity in vitro
  publication-title: Gene
  doi: 10.1016/j.gene.2018.05.106
– volume: 10
  start-page: 105
  year: 2020
  ident: CR12
  article-title: Antifungal peptides as therapeutic agents
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2020.00105
– volume: 21
  start-page: e13093
  issue: 12
  year: 2019
  ident: CR21
  article-title: Variations in yeast plasma-membrane lipid composition affect killing activity of three families of insect antifungal peptides
  publication-title: Cell Microbiol
  doi: 10.1111/cmi.13093
– volume: 16
  start-page: 603
  issue: 9
  year: 2017
  end-page: 616
  ident: CR46
  article-title: The antifungal pipeline: a reality check
  publication-title: Nat Rev Drug Discov
  doi: 10.1038/nrd.2017.46
– volume: 479
  start-page: 103
  issue: 1
  year: 2016
  end-page: 108
  ident: CR32
  article-title: Mechanism of action and in vitro activity of short hybrid antimicrobial peptide PV3 against
  publication-title: Biochem Biophys Res Commun
  doi: 10.1016/j.bbrc.2016.09.045
– volume: 15
  start-page: e0009092
  issue: 2
  year: 2021
  ident: CR40
  article-title: The impact of COVID-19 pandemic on AIDS-related mycoses and fungal neglected tropical diseases: why should we worry?
  publication-title: PLoS Negl Trop Dis
  doi: 10.1371/journal.pntd.0009092
– volume: 13
  start-page: 287
  year: 2021
  end-page: 298
  ident: CR52
  article-title: Effect of Dermaseptin S4 on growth and and gene expression
  publication-title: Probiotics Antimicro Prot
  doi: 10.1007/s12602-020-09685-0
– volume: 49
  start-page: 1340
  issue: 4
  year: 2005
  end-page: 1345
  ident: CR53
  article-title: Bactericidal and antiendotoxic properties of short cationic peptides derived from a snake venom Lys49 phospholipase A
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.49.4.1340-1345.2005
– ident: CR10
– volume: 5
  start-page: 725
  issue: 4
  year: 2010
  end-page: 738
  ident: CR51
  article-title: I-TASSER: a unified platform for automated protein structure and function prediction
  publication-title: Nat Protoc
  doi: 10.1038/nprot.2010.5
– volume: 13
  start-page: 89
  issue: 1
  year: 2022
  end-page: 121
  ident: CR25
  article-title: Pathogenesis and virulence of
  publication-title: Virulence
  doi: 10.1080/21505594.2021.2019950
– volume: 8
  start-page: 1018
  issue: 10
  year: 2022
  ident: CR60
  article-title: 2,4-Diacetylphloroglucinol modulates Virulence
  publication-title: J Fungi
  doi: 10.3390/jof8101018
– volume: 10
  start-page: 859
  issue: 7
  year: 2021
  ident: CR8
  article-title: From jekyll to hyde: the yeast–hyphal transition of
  publication-title: Pathogens
  doi: 10.3390/pathogens10070859
– volume: 141
  start-page: 528
  year: 2016
  end-page: 536
  ident: CR16
  article-title: Role of amphipathicity and hydrophobicity in the balance between hemolysis and peptide–membrane interactions of three related antimicrobial peptides
  publication-title: Colloids Surf B Biointerfaces
  doi: 10.1016/j.colsurfb.2016.02.003
– volume: 21
  start-page: 47
  year: 2015
  end-page: 55
  ident: CR2
  article-title: Cationic antimicrobial peptides cytotoxicity on mammalian cells: an analysis using therapeutic index integrative concept
  publication-title: Int J Pept Res Ther
  doi: 10.1007/s10989-014-9430-z
– volume: 27
  start-page: 751
  issue: 5
  year: 2004
  end-page: 752
  ident: CR54
  article-title: Farnesol, a morphogenetic autoregulatory substance in the dimorphic fungus , inhibits hyphae growth through suppression of a mitogen-activated protein kinase cascade
  publication-title: Biol Pharm Bull
  doi: 10.1248/bpb.27.751
– volume: 2021
  start-page: 5597758
  year: 2021
  ident: CR37
  article-title: Evaluation of fibroblast viability seeded on acellular human amniotic membrane
  publication-title: BioMed Res Int
  doi: 10.1155/2021/5597758
– volume: 30
  start-page: 1589
  issue: 11
  year: 2022
  end-page: 1601
  ident: CR4
  article-title: Deep tissue infection by an invasive human fungal pathogen requires lipid-based suppression of the IL-17 response
  publication-title: Cell Host Microbe
  doi: 10.1016/j.chom.2022.10.004
– volume: 6
  start-page: 27258
  year: 2016
  ident: CR27
  article-title: Antimicrobial activity, improved cell selectivity and mode of action of short PMAP-36-derived peptides against bacteria and
  publication-title: Sci Rep
  doi: 10.1038/srep27258
– volume: 39
  start-page: 831
  issue: 3
  year: 2019
  end-page: 859
  ident: CR65
  article-title: Antimicrobial peptides: PROMISING alternatives in the post feeding antibiotic era
  publication-title: Med Res Rev
  doi: 10.1002/med.21542
– volume: 47
  start-page: 47
  issue: 1–2
  year: 1996
  end-page: 55
  ident: CR58
  article-title: Highthroughput purity estimation and characterisation of synthetic peptides by electrospray mass spectrometry
  publication-title: Int J Pept Protein Res
  doi: 10.1111/j.1399-3011.1996.tb00809.x
– ident: CR44
– volume: 7
  start-page: 249
  year: 2017
  ident: CR14
  article-title: d1 effects on planktonic cells and biofilms
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2017.00249
– volume: 10
  start-page: 2732
  year: 2020
  end-page: 2744
  ident: CR39
  article-title: Helicity modulation improves the selectivity of antimicrobial peptoids
  publication-title: ACS Infect Dis
  doi: 10.1021/acsinfecdis.0c00356
– volume: 5
  start-page: 9657
  year: 2015
  ident: CR26
  article-title: Activity of novel synthetic peptides against
  publication-title: Sci Rep
  doi: 10.1038/srep09657
– volume: 20
  start-page: 1953
  issue: 4
  year: 2013
  end-page: 1959
  ident: CR41
  article-title: Influence of additives on [Beta]-glucan production
  publication-title: Int Food Res J
– volume: 1
  start-page: 16162
  year: 2016
  ident: CR24
  article-title: Combating multidrug-resistant Gram-negative bacteria with structurally nanoengineered antimicrobial peptide polymers
  publication-title: Nat Microbiol
  doi: 10.1038/nmicrobiol.2016.162
– volume: 25
  start-page: 911
  issue: 3
  year: 2019
  end-page: 918
  ident: CR1
  article-title: Synthesis, characterization and lipophilicity study of ’ immunogenic peptide sequence that can be used in the future vaccination studies
  publication-title: Int J Pept Res Ther
  doi: 10.1007/s10989-018-9739-0
– volume: 24
  start-page: 1584
  issue: 2
  year: 2023
  ident: CR13
  article-title: Pathogenic drug resistant fungi: a review of mitigation strategies
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms24021584
– volume: 5
  start-page: 21
  issue: 1
  year: 2019
  ident: CR22
  article-title: Regulation of hyphal morphogenesis by endogenous signals
  publication-title: J Fungi
  doi: 10.3390/jof5010021
– volume: 15
  start-page: 96
  issue: 2
  year: 2017
  end-page: 108
  ident: CR42
  article-title: cell-type switching and functional plasticity in the mammalian host
  publication-title: Nat Rev Microbiol
  doi: 10.1038/nrmicro.2016.157
– volume: 89
  start-page: 327
  year: 2017
  end-page: 338
  ident: CR33
  article-title: Design and characterization of short hybrid antimicrobial peptides from pEM-2, mastoparan-VT 1, and mastoparan-B
  publication-title: Chem Biol Drug Des
  doi: 10.1111/cbdd.12864
– volume: 74
  start-page: 151
  year: 2013
  end-page: 157
  ident: CR67
  article-title: Antimicrobial peptides from the venom gland of the social wasp
  publication-title: Toxicon
  doi: 10.1016/j.toxicon.2013.08.056
– volume: 32
  start-page: 1732
  year: 2011
  end-page: 1740
  ident: CR29
  article-title: Antifungal activity of novel synthetic peptides by accumulation of reactive oxygen species (ROS) and disruption of cell wall against
  publication-title: Peptides
  doi: 10.1016/j.peptides.2011.06.003
– volume: 13
  start-page: 246
  year: 2013
  ident: CR61
  article-title: growth, transition, biofilm formation, and gene expression modulation by antimicrobial decapeptide KSL-W
  publication-title: BMC Microbiol
  doi: 10.1186/1471-2180-13-246
– volume: 43
  start-page: 2279
  year: 2012
  end-page: 2283
  ident: CR64
  article-title: Chemical synthesis and biological evaluation of an antimicrobial peptide gonococcal growth inhibitor
  publication-title: Amino Acids
  doi: 10.1007/s00726-012-1305-z
– volume: 130
  start-page: 132
  year: 2016
  end-page: 145
  ident: CR48
  article-title: Antifungal peptides: to be or not to be membrane active
  publication-title: Biochimie
  doi: 10.1016/j.biochi.2016.05.013
– volume: 21
  start-page: 47
  year: 2015
  ident: 10525_CR2
  publication-title: Int J Pept Res Ther
  doi: 10.1007/s10989-014-9430-z
– volume: 8
  start-page: 1018
  issue: 10
  year: 2022
  ident: 10525_CR60
  publication-title: J Fungi
  doi: 10.3390/jof8101018
– volume: 36
  start-page: 793
  issue: 6
  year: 1995
  ident: 10525_CR43
  publication-title: Biopolymers
  doi: 10.1002/bip.360360611
– volume: 12
  start-page: 7
  issue: 1
  year: 2015
  ident: 10525_CR68
  publication-title: Nat Methods
  doi: 10.1038/nmeth.3213
– volume: 13
  start-page: 313
  year: 2021
  ident: 10525_CR28
  publication-title: Future Med Chem
  doi: 10.4155/fmc-2020-0052
– volume: 10
  start-page: 85
  issue: 1
  year: 2012
  ident: 10525_CR18
  publication-title: Expert Rev Anti Infect Ther
  doi: 10.1586/eri.11.152
– volume: 13
  start-page: 5352
  issue: 1
  year: 2022
  ident: 10525_CR15
  publication-title: Nat Commun
  doi: 10.1038/s41467-022-32249-5
– volume: 5
  start-page: 21
  issue: 1
  year: 2019
  ident: 10525_CR22
  publication-title: J Fungi
  doi: 10.3390/jof5010021
– volume: 5
  start-page: 725
  issue: 4
  year: 2010
  ident: 10525_CR51
  publication-title: Nat Protoc
  doi: 10.1038/nprot.2010.5
– volume: 47
  start-page: 47
  issue: 1–2
  year: 1996
  ident: 10525_CR58
  publication-title: Int J Pept Protein Res
  doi: 10.1111/j.1399-3011.1996.tb00809.x
– volume: 24
  start-page: 1584
  issue: 2
  year: 2023
  ident: 10525_CR13
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms24021584
– volume: 5
  start-page: 9657
  year: 2015
  ident: 10525_CR26
  publication-title: Sci Rep
  doi: 10.1038/srep09657
– ident: 10525_CR10
  doi: 10.1038/s41598-020-67041-2
– volume: 20
  start-page: 1953
  issue: 4
  year: 2013
  ident: 10525_CR41
  publication-title: Int Food Res J
– volume: 9
  start-page: 171
  issue: 2
  year: 2023
  ident: 10525_CR63
  publication-title: J Fungi
  doi: 10.3390/jof9020171
– volume: 10
  start-page: 105
  year: 2020
  ident: 10525_CR12
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2020.00105
– volume: 1
  start-page: 16162
  year: 2016
  ident: 10525_CR24
  publication-title: Nat Microbiol
  doi: 10.1038/nmicrobiol.2016.162
– volume: 10
  start-page: 859
  issue: 7
  year: 2021
  ident: 10525_CR8
  publication-title: Pathogens
  doi: 10.3390/pathogens10070859
– volume: 12
  start-page: 1581
  issue: 10
  year: 2022
  ident: 10525_CR45
  publication-title: Life (basel)
  doi: 10.3390/life12101581
– volume: 130
  start-page: 132
  year: 2016
  ident: 10525_CR48
  publication-title: Biochimie
  doi: 10.1016/j.biochi.2016.05.013
– volume: 25
  start-page: 911
  issue: 3
  year: 2019
  ident: 10525_CR1
  publication-title: Int J Pept Res Ther
  doi: 10.1007/s10989-018-9739-0
– ident: 10525_CR9
– volume: 67
  start-page: 349
  issue: 4
  year: 2014
  ident: 10525_CR62
  publication-title: J Antibiot (tokyo)
  doi: 10.1038/ja.2013.140
– volume: 39
  start-page: 99
  issue: 4
  year: 2023
  ident: 10525_CR31
  publication-title: World J Microbiol Biotechnol
  doi: 10.1007/s11274-023-03545
– volume: 12
  start-page: e0180680
  issue: 7
  year: 2017
  ident: 10525_CR35
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0180680
– volume: 479
  start-page: 103
  issue: 1
  year: 2016
  ident: 10525_CR32
  publication-title: Biochem Biophys Res Commun
  doi: 10.1016/j.bbrc.2016.09.045
– volume: 89
  start-page: 327
  year: 2017
  ident: 10525_CR33
  publication-title: Chem Biol Drug Des
  doi: 10.1111/cbdd.12864
– volume: 52
  start-page: 1439
  year: 2020
  ident: 10525_CR11
  publication-title: Amino Acids
  doi: 10.1007/s00726-020-02903-7
– volume: 2021
  start-page: 5597758
  year: 2021
  ident: 10525_CR37
  publication-title: BioMed Res Int
  doi: 10.1155/2021/5597758
– volume: 8
  start-page: 59
  year: 2021
  ident: 10525_CR5
  publication-title: Curr Trop Med Rep
  doi: 10.1007/s40475-021-00226-5
– volume: 10
  start-page: 1004
  issue: 8
  year: 2011
  ident: 10525_CR57
  publication-title: Eukaryot Cell
  doi: 10.1128/EC.05030-11
– volume: 193
  start-page: 2591
  issue: 8
  year: 2021
  ident: 10525_CR7
  publication-title: Appl Biochem Biotechnol
  doi: 10.1007/s12010-021-03553-5
– volume: 39
  start-page: 831
  issue: 3
  year: 2019
  ident: 10525_CR65
  publication-title: Med Res Rev
  doi: 10.1002/med.21542
– volume: 9
  start-page: 454
  issue: 8
  year: 2020
  ident: 10525_CR19
  publication-title: Antibiotics
  doi: 10.3390/antibiotics9080454
– volume: 9
  start-page: 1490
  issue: 1
  year: 2018
  ident: 10525_CR47
  publication-title: Nat Commun
  doi: 10.1038/s41467-018-03746-3
– volume: 11
  start-page: 20621
  issue: 1
  year: 2021
  ident: 10525_CR3
  publication-title: Sci Rep
  doi: 10.1038/s41598-021-00223-8
– volume: 16
  start-page: 603
  issue: 9
  year: 2017
  ident: 10525_CR46
  publication-title: Nat Rev Drug Discov
  doi: 10.1038/nrd.2017.46
– volume: 15
  start-page: 96
  issue: 2
  year: 2017
  ident: 10525_CR42
  publication-title: Nat Rev Microbiol
  doi: 10.1038/nrmicro.2016.157
– volume: 21
  start-page: 853
  issue: 12
  year: 2015
  ident: 10525_CR36
  publication-title: J Pept Sci
  doi: 10.1002/psc.2827
– volume: 15
  start-page: e0009092
  issue: 2
  year: 2021
  ident: 10525_CR40
  publication-title: PLoS Negl Trop Dis
  doi: 10.1371/journal.pntd.0009092
– volume: 21
  start-page: e13093
  issue: 12
  year: 2019
  ident: 10525_CR21
  publication-title: Cell Microbiol
  doi: 10.1111/cmi.13093
– volume: 20
  start-page: 501
  issue: 8
  year: 2022
  ident: 10525_CR55
  publication-title: Mar Drugs
  doi: 10.3390/md20080501
– volume: 396
  start-page: 1441
  year: 2010
  ident: 10525_CR56
  publication-title: Anal Bioanal Chem
  doi: 10.1007/s00216-009-3316-5
– volume: 13
  start-page: 89
  issue: 1
  year: 2022
  ident: 10525_CR25
  publication-title: Virulence
  doi: 10.1080/21505594.2021.2019950
– volume: 60
  start-page: 5894
  issue: 10
  year: 2016
  ident: 10525_CR49
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.00190-16
– volume: 162
  start-page: 164
  year: 2011
  ident: 10525_CR23
  publication-title: Res Microbiol
  doi: 10.1016/j.resmic.2010.11.006
– ident: 10525_CR44
  doi: 10.5772/intechopen.99737
– volume: 49
  start-page: 1340
  issue: 4
  year: 2005
  ident: 10525_CR53
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.49.4.1340-1345.2005
– volume: 6
  start-page: 27258
  year: 2016
  ident: 10525_CR27
  publication-title: Sci Rep
  doi: 10.1038/srep27258
– volume: 441
  start-page: 963
  issue: 3
  year: 2012
  ident: 10525_CR6
  publication-title: Biochem J
  doi: 10.1042/BJ20111454
– volume: 74
  start-page: 151
  year: 2013
  ident: 10525_CR67
  publication-title: Toxicon
  doi: 10.1016/j.toxicon.2013.08.056
– volume: 46
  start-page: 273
  year: 2021
  ident: 10525_CR17
  publication-title: Profiles Drug Subst Excip Relat Methodol
  doi: 10.1016/bs.podrm.2020.07.005
– volume: 141
  start-page: 528
  year: 2016
  ident: 10525_CR16
  publication-title: Colloids Surf B Biointerfaces
  doi: 10.1016/j.colsurfb.2016.02.003
– volume: 21
  start-page: 1912
  year: 2020
  ident: 10525_CR59
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms21061912
– volume: 32
  start-page: 1732
  year: 2011
  ident: 10525_CR29
  publication-title: Peptides
  doi: 10.1016/j.peptides.2011.06.003
– volume: 48
  start-page: 369
  year: 2004
  ident: 10525_CR38
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.48.2.369-377.2004
– volume: 43
  start-page: 2279
  year: 2012
  ident: 10525_CR64
  publication-title: Amino Acids
  doi: 10.1007/s00726-012-1305-z
– volume: 13
  start-page: 287
  year: 2021
  ident: 10525_CR52
  publication-title: Probiotics Antimicro Prot
  doi: 10.1007/s12602-020-09685-0
– volume: 28
  start-page: 96
  year: 2022
  ident: 10525_CR34
  publication-title: Int J Pept Res Ther
  doi: 10.1007/s10989-022-10401-5
– volume: 20
  start-page: 5713
  year: 2019
  ident: 10525_CR50
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms20225713
– volume: 13
  start-page: 246
  year: 2013
  ident: 10525_CR61
  publication-title: BMC Microbiol
  doi: 10.1186/1471-2180-13-246
– volume: 104
  start-page: 6513
  year: 2020
  ident: 10525_CR30
  publication-title: Appl Microbiol Biotechnol
  doi: 10.1007/s00253-020-10701-0
– volume: 10
  start-page: 2732
  year: 2020
  ident: 10525_CR39
  publication-title: ACS Infect Dis
  doi: 10.1021/acsinfecdis.0c00356
– volume: 30
  start-page: 1589
  issue: 11
  year: 2022
  ident: 10525_CR4
  publication-title: Cell Host Microbe
  doi: 10.1016/j.chom.2022.10.004
– volume: 1859
  start-page: 1851
  year: 2017
  ident: 10525_CR20
  publication-title: Biochim Biophys Acta Biomembr
  doi: 10.1016/j.bbamem.2017.06.005
– volume: 27
  start-page: 751
  issue: 5
  year: 2004
  ident: 10525_CR54
  publication-title: Biol Pharm Bull
  doi: 10.1248/bpb.27.751
– volume: 671
  start-page: 1
  year: 2018
  ident: 10525_CR66
  publication-title: Gene
  doi: 10.1016/j.gene.2018.05.106
– volume: 7
  start-page: 249
  year: 2017
  ident: 10525_CR14
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2017.00249
SSID ssj0052710
Score 2.2969637
Snippet Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid,...
SourceID proquest
crossref
springer
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 50
SubjectTerms Animal Anatomy
Antimicrobial peptides
Atomic force microscopy
Biochemistry
Biomedical and Life Sciences
Cell walls
Circular dichroism
Conformation
Cytotoxicity
Drug resistance
Fourier transforms
Histology
Life Sciences
Microbicides
Minimum inhibitory concentration
Molecular Medicine
Morphology
Peptides
Pharmaceutical Sciences/Technology
Pharmacology/Toxicology
Polymer Sciences
Polysaccharides
Yeast
SummonAdditionalLinks – databaseName: SpringerLink Journals (ICM)
  dbid: U2A
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3NS8MwFA8yD3oR3RSnU3IQLxpI06Qfx1IcQ5gIOtitNB_FguvETsH_3pe0dSoqeCtJXg59Sd7vfSN05rHCj3LNCPfygnBGJckjowgPBVwvasvh2dzh6U0wmfHruZi3SWF1F-3euSTdS_0p2c2F9zAbSyWYIPDwbgqru8MpnrGke38FA6HZpsf8TPdVBK1x5TdXqJMw412000JDnDS83EMbpuqjQVKBWrx4w-fYBWs6K3gfbaVdo7YBypPKGqQrXWpLrpp-EBgG8NTYxN6yXuBl4WaWlf26M6_WFIXTxhyrcPpQOs8NtlstSlecCeZvbciLNvU-mo2v7tMJaTsnEAVXakVMyLnwYxUWIMCLEFQ4RTnXlBYAv3QYS07zQPuKWbxClW88yY3xeaBynstA-geoVy0rc4hwXBSMAxmgcMMjrqXxlM8iQ2MVSR2IIfK6n5mptqy47W7xmK0LIlsGZMCAzDEgY0N08UHz1BTV-HP1qONR1l6wOmORZ9EbqNhDdNnxbT39-25H_1t-jLZtg3kX4hiMUG_1_GJOAIas5Kk7de8xa9NY
  priority: 102
  providerName: Springer Nature
Title Anticandidal Activity and Mechanism of Action of Several Cationic Chimeric Antimicrobial Peptides
URI https://link.springer.com/article/10.1007/s10989-023-10525-2
https://www.proquest.com/docview/2810250713
Volume 29
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3NS8MwFH_oPOhF_MT5RQ7iRYNtmn6dpI5NUTZEHcxTaZMUB65TNwX_e_PSdEPBnVqSJoe-JO8jv_d-ACcuK7wok4xyNysoZ05Os0gJykNfby8Hy-Fh7nC3F9z0-e3AH9iA28TCKusz0RzUciwwRn7BIhfVtfapLt_eKbJG4e2qpdBYhhUsXYaQrnAwc7h8FlbVCPwQc8h4bJNmbOqcAQsxRGb5zKfst2KaW5t_LkiN3ulswLo1GElSSXgTllS5BdtJqZ3l0Tc5JQbCaWLjW7DaqunbtiFLSgxTl3IocbioWCKIbiBdhem-w8mIjAvTMy7x7VF9YYCKtKogrSCtl6G5zyE41WhoSjbp_nsEwkg12YF-p_3UuqGWT4EKvdGmVIWc-14swkKr9SLUjp1wOJeOU2ijTIZxzp0skJ5gaMU4wlNuzpXyeCAynuVB7u1CoxyXag9IXBSM62HaNlc84jJXrvBYpJxYRLkM_Ca49c9MhS02jpwXr-m8TDIKINUCSI0AUtaEs9mYt6rUxsKvD2sZpXbbTdL5ImnCeS23eff_s-0vnu0A1pBm3gAdg0NoTD8-1ZE2Rqb5sVlxx7CSXD_ftfXzqt27f9CtfZb8AChY3Ec
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LT9wwEB7R5UAviFfVLZT6ULhQq4kzeR2qarsFLYVdoRYkbmliO-pKbBbYhYo_1d_YGSfpqpXKjVsU23PwjD0Pz8wH8NZXZZDkRkn081Ki8gqZJ1ZLjEM6Xh63w-Pa4eEoGlzgl8vwcgl-tbUwnFbZ3onuojZTzTHy9yrxWV2TT_Xx-kYyahS_rrYQGrVYnNiHn-SyzT4cfyb-7il1dHjeH8gGVUBqEre5tDFiGKQ6Lkm5lTG5N9pDNJ5Xkmli4rRAL49MoBXrck8H1i_Q2gAjnWNeREVAdJ_BMgbkynRg-dPh6Oxre_eHKq77H4QxV61h2pTpNMV6Lj1JcS5YqEKp_laFC_v2nydZp-mO1mC1MVFFr5apdViy1QZs9ipyzycPYl-4pFEXjd-AlX4LGLcJea_iwHhlxoaX6xqXQtAPMbRcYDyeTcS0dCPTir--2XsOiYl-HRbWov9j7F6QBJOajF2TKBo_49QbY2dbcPEke_0COtW0si9BpGWpkJaRN2AxQVNYXwcqsV6qk8JEYRf8djMz3bQ3Z5SNq2zRmJkZkBEDMseATHXh4M-a67q5x6Ozd1oeZc1Bn2ULsezCu5Zvi-H_U3v1OLU3sDI4H55mp8ejk214ziD3Ls0y2oHO_PbOviZTaF7sNvIn4PtTi_xv8YIVcg
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LT9wwEB5RkGgvFYVWbAvUh8KltUgcO04OCK2WrqA8hNQi7S1N_FBX6mZpd9uKv9Zfx4yTsGoluHGLYnsOnrHn4W9mAN7FwidZaQWXcem5FFHFy8wZLrXC4xVROTzKHT6_SI-v5KeRGi3B3y4XhmCV3Z0YLmo7NRQj3xdZTOoafap938IiLo-Gh9c_OHWQopfWrp1GIyKn7uYPum-zg5Mj5PWuEMOPXwbHvO0wwA2K3pw7LaVKcqM9Kjqv0dUxkZQ2ijyaKVbnlYzK1CZGkF6PTOLiSjqXyNSUsqzSKkG6T2BFJyqmM6ZHd86eErqphKA05a_JvE3YadP2AlBJECpMCcXFv0pxYen-9zgbdN5wDZ63xirrN9L1ApZcvQ4b_Rod9ckN22MBPhri8uvwdNC1jtuAsl9TiLy2Y0vLTdOhguEPdu4o1Xg8m7CpDyPTmr4-u98UHGODJkBs2ODbOLwlMSI1GYdyUTh-SSAc62Yv4epRdvoVLNfT2m0Cy70XEpehX-BkJm3lYpOIzEW5ySqbqh7E3WYWpi10Tv02vheLEs3EgAIZUAQGFKIH7-_WXDdlPh6cvdXxqGiP_KxYCGgPPnR8WwzfT-31w9TewioKenF2cnH6Bp5Rt_uAt0y3YHn-85fbRptoXu0E4WPw9bGl_RYlhRhC
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Anticandidal+Activity+and+Mechanism+of+Action+of+Several+Cationic+Chimeric+Antimicrobial+Peptides&rft.jtitle=International+journal+of+peptide+research+and+therapeutics&rft.au=Memariani%2C+Mojtaba&rft.au=Memariani%2C+Hamed&rft.au=Moravvej%2C+Hamideh&rft.au=Goudarzi%2C+Hossein&rft.date=2023-05-06&rft.pub=Springer+Nature+B.V&rft.issn=1573-3149&rft.eissn=1573-3904&rft.volume=29&rft.issue=3&rft.spage=50&rft_id=info:doi/10.1007%2Fs10989-023-10525-2&rft.externalDBID=HAS_PDF_LINK
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1573-3904&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1573-3904&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1573-3904&client=summon