Epitope mapping by solution NMR spectroscopy

Antibodies play an ever more prominent role in basic research as well as in the biotechnology and pharmaceutical sectors. Characterizing their epitopes, that is, the region that they recognize on their target molecule, is useful for purposes ranging from molecular biology research to vaccine design...

Full description

Saved in:
Bibliographic Details
Published inJournal of molecular recognition Vol. 28; no. 6; pp. 393 - 400
Main Authors Bardelli, M., Livoti, E., Simonelli, L., Pedotti, M., Moraes, A., Valente, A. P., Varani, L.
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.06.2015
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Antibodies play an ever more prominent role in basic research as well as in the biotechnology and pharmaceutical sectors. Characterizing their epitopes, that is, the region that they recognize on their target molecule, is useful for purposes ranging from molecular biology research to vaccine design and intellectual property protection. Solution NMR spectroscopy is ideally suited to the atomic level characterization of intermolecular interfaces and, as a consequence, to epitope discovery. Here, we illustrate how NMR epitope mapping can be used to rapidly and accurately determine protein antigen epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody will identify epitope residues. NMR epitope mapping provides more detailed information than mutagenesis or peptide mapping and can be much more rapid than X‐ray crystallography. Advantages and drawbacks of this technique are discussed together with practical considerations. Copyright © 2015 John Wiley & Sons, Ltd. Characterization of antibody epitopes has useful implications for both basic research and the biotechnology sectors. Solution NMR spectroscopy is a powerful and yet relatively unknown tool for the determination of epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody can identify epitope residues. The article describes advantages and drawbacks of this approach, including practical considerations.
AbstractList Antibodies play an ever more prominent role in basic research as well as in the biotechnology and pharmaceutical sectors. Characterizing their epitopes, that is, the region that they recognize on their target molecule, is useful for purposes ranging from molecular biology research to vaccine design and intellectual property protection. Solution NMR spectroscopy is ideally suited to the atomic level characterization of intermolecular interfaces and, as a consequence, to epitope discovery. Here, we illustrate how NMR epitope mapping can be used to rapidly and accurately determine protein antigen epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody will identify epitope residues. NMR epitope mapping provides more detailed information than mutagenesis or peptide mapping and can be much more rapid than X-ray crystallography. Advantages and drawbacks of this technique are discussed together with practical considerations. Copyright copyright 2015 John Wiley & Sons, Ltd. Characterization of antibody epitopes has useful implications for both basic research and the biotechnology sectors. Solution NMR spectroscopy is a powerful and yet relatively unknown tool for the determination of epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody can identify epitope residues. The article describes advantages and drawbacks of this approach, including practical considerations.
Antibodies play an ever more prominent role in basic research as well as in the biotechnology and pharmaceutical sectors. Characterizing their epitopes, that is, the region that they recognize on their target molecule, is useful for purposes ranging from molecular biology research to vaccine design and intellectual property protection. Solution NMR spectroscopy is ideally suited to the atomic level characterization of intermolecular interfaces and, as a consequence, to epitope discovery. Here, we illustrate how NMR epitope mapping can be used to rapidly and accurately determine protein antigen epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody will identify epitope residues. NMR epitope mapping provides more detailed information than mutagenesis or peptide mapping and can be much more rapid than X-ray crystallography. Advantages and drawbacks of this technique are discussed together with practical considerations. Copyright © 2015 John Wiley & Sons, Ltd.
Antibodies play an ever more prominent role in basic research as well as in the biotechnology and pharmaceutical sectors. Characterizing their epitopes, that is, the region that they recognize on their target molecule, is useful for purposes ranging from molecular biology research to vaccine design and intellectual property protection. Solution NMR spectroscopy is ideally suited to the atomic level characterization of intermolecular interfaces and, as a consequence, to epitope discovery. Here, we illustrate how NMR epitope mapping can be used to rapidly and accurately determine protein antigen epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody will identify epitope residues. NMR epitope mapping provides more detailed information than mutagenesis or peptide mapping and can be much more rapid than X-ray crystallography. Advantages and drawbacks of this technique are discussed together with practical considerations.
Antibodies play an ever more prominent role in basic research as well as in the biotechnology and pharmaceutical sectors. Characterizing their epitopes, that is, the region that they recognize on their target molecule, is useful for purposes ranging from molecular biology research to vaccine design and intellectual property protection. Solution NMR spectroscopy is ideally suited to the atomic level characterization of intermolecular interfaces and, as a consequence, to epitope discovery. Here, we illustrate how NMR epitope mapping can be used to rapidly and accurately determine protein antigen epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody will identify epitope residues. NMR epitope mapping provides more detailed information than mutagenesis or peptide mapping and can be much more rapid than X‐ray crystallography. Advantages and drawbacks of this technique are discussed together with practical considerations. Copyright © 2015 John Wiley & Sons, Ltd. Characterization of antibody epitopes has useful implications for both basic research and the biotechnology sectors. Solution NMR spectroscopy is a powerful and yet relatively unknown tool for the determination of epitopes. The basic concept is that differences in the NMR signal of an antigen free or bound by an antibody can identify epitope residues. The article describes advantages and drawbacks of this approach, including practical considerations.
Author Livoti, E.
Valente, A. P.
Varani, L.
Simonelli, L.
Moraes, A.
Bardelli, M.
Pedotti, M.
Author_xml – sequence: 1
  givenname: M.
  surname: Bardelli
  fullname: Bardelli, M.
  organization: Institute for Research in Biomedicine
– sequence: 2
  givenname: E.
  surname: Livoti
  fullname: Livoti, E.
  organization: Institute for Research in Biomedicine
– sequence: 3
  givenname: L.
  surname: Simonelli
  fullname: Simonelli, L.
  organization: Institute for Research in Biomedicine
– sequence: 4
  givenname: M.
  surname: Pedotti
  fullname: Pedotti, M.
  organization: Institute for Research in Biomedicine
– sequence: 5
  givenname: A.
  surname: Moraes
  fullname: Moraes, A.
  organization: Universidade Federal do Rio de Janeiro, Centro Nacional de Ressonância Magnética Nuclear Jiri Jonas
– sequence: 6
  givenname: A. P.
  surname: Valente
  fullname: Valente, A. P.
  organization: Universidade Federal do Rio de Janeiro, Centro Nacional de Ressonância Magnética Nuclear Jiri Jonas
– sequence: 7
  givenname: L.
  surname: Varani
  fullname: Varani, L.
  organization: Institute for Research in Biomedicine
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25726811$$D View this record in MEDLINE/PubMed
BookMark eNp1kFtLwzAUgINM3EXBXyAFX3ywmmvTPMqYNzaFsfeQpql0tE1sWqT_3sxNBcGn83A-Ps75pmDU2MYAcI7gDYIQ327r9gZTRo_ABEEhYkQYHoEJFAzHhAoxBlPvtxCGHYMnYIwZx0mK0ARcL1zZWWeiWjlXNm9RNkTeVn1X2iZ6Wa0j74zuWuu1dcMpOC5U5c3ZYc7A5n6xmT_Gy9eHp_ndMtZYcBonRcGLvGCMYkG4FhRlAqVMEaQVyVOW5wlTKeVKCwIzLkhCYQ4LmhnDRJKTGbjaa11r33vjO1mXXpuqUo2xvZcoSVkKMUQkoJd_0K3t2yYcFyhOKRIw4b9CHR7xrSmka8tatYNEUO4CyhBQ7gIG9OIg7LPa5D_gd7EAxHvgo6zM8K9IPq_WX8JPEwx5Ew
CitedBy_id crossref_primary_10_3390_biom14030374
crossref_primary_10_1590_1678_9199_jvatitd_2019_0013
crossref_primary_10_1021_acs_analchem_3c04161
crossref_primary_10_3390_antib12040067
crossref_primary_10_1039_D1CB00051A
crossref_primary_10_3390_vaccines11071176
crossref_primary_10_1016_j_jmb_2015_05_016
crossref_primary_10_1016_j_ecoenv_2021_112925
crossref_primary_10_1016_j_jmro_2023_100093
crossref_primary_10_1093_abbs_gmab020
crossref_primary_10_1177_25151355221100218
crossref_primary_10_1002_jmr_2778
crossref_primary_10_1038_s42003_024_06363_7
crossref_primary_10_1016_j_cell_2017_09_002
crossref_primary_10_1016_j_coviro_2021_04_001
crossref_primary_10_1155_2015_156241
crossref_primary_10_1016_j_ab_2023_115319
crossref_primary_10_1038_s41598_019_49061_9
crossref_primary_10_3389_frans_2023_1118749
crossref_primary_10_1016_j_addr_2022_114142
crossref_primary_10_1021_jasms_3c00069
crossref_primary_10_1038_s41598_023_40467_0
crossref_primary_10_1074_mcp_RA119_001429
crossref_primary_10_1007_s13361_017_1883_9
crossref_primary_10_1021_acs_jmedchem_1c00852
crossref_primary_10_1021_jasms_2c00255
crossref_primary_10_1080_19420862_2017_1379641
crossref_primary_10_1128_JVI_02314_15
crossref_primary_10_1021_acs_analchem_2c03091
crossref_primary_10_1039_D1NR03180E
crossref_primary_10_1016_j_celrep_2024_114298
crossref_primary_10_1080_19420862_2023_2285285
crossref_primary_10_3390_biom14010024
Cites_doi 10.1016/j.jmb.2012.09.021
10.1007/BF00176005
10.1016/j.pnmrs.2013.12.001
10.1021/bi0301237
10.1016/j.molbiopara.2004.06.014
10.1126/science.3140379
10.1093/nar/gkm957
10.1042/BJ20120884
10.1016/j.jmb.2009.04.019
10.1021/ja026939x
10.1016/j.jmb.2007.09.030
10.1016/S0959-440X(99)00011-1
10.1021/bi9712091
10.1016/j.jmr.2011.08.010
10.1016/0079-6107(94)90010-8
10.1007/s10858-009-9362-7
10.1074/jbc.M010812200
10.1038/nbt.2291
10.1002/cbic.201200732
10.1007/BF02789290
10.1016/j.str.2010.05.012
10.1038/nprot.2010.32
10.1126/science.2047852
10.1021/bi00471a022
10.1016/S0076-6879(80)70045-9
10.1016/j.jmb.2009.12.053
10.1002/prot.21723
10.1016/j.jmr.2004.11.021
10.1016/j.jmr.2011.09.009
10.1021/ja101842n
10.1016/j.pnmrs.2003.08.001
10.1074/jbc.M109.025304
10.1038/73331
10.1023/B:JNMR.0000042954.99056.ad
10.1016/S0969-2126(00)00119-2
10.1016/j.pnmrs.2013.02.001
10.1038/nbt1363
10.1073/pnas.0703702104
10.3390/ijms12010226
10.1089/cmb.2010.0251
10.1021/bi011870b
10.1371/journal.pone.0055561
ContentType Journal Article
Copyright Copyright © 2015 John Wiley & Sons, Ltd.
Copyright_xml – notice: Copyright © 2015 John Wiley & Sons, Ltd.
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7QF
7QO
7QP
7QQ
7SE
7SR
7TA
7TK
7TM
8BQ
8FD
F28
FR3
H8G
JG9
P64
7U5
L7M
DOI 10.1002/jmr.2454
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
Aluminium Industry Abstracts
Biotechnology Research Abstracts
Calcium & Calcified Tissue Abstracts
Ceramic Abstracts
Corrosion Abstracts
Engineered Materials Abstracts
Materials Business File
Neurosciences Abstracts
Nucleic Acids Abstracts
METADEX
Technology Research Database
ANTE: Abstracts in New Technology & Engineering
Engineering Research Database
Copper Technical Reference Library
Materials Research Database
Biotechnology and BioEngineering Abstracts
Solid State and Superconductivity Abstracts
Advanced Technologies Database with Aerospace
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
Materials Research Database
Aluminium Industry Abstracts
Technology Research Database
Nucleic Acids Abstracts
Ceramic Abstracts
Neurosciences Abstracts
Materials Business File
METADEX
Biotechnology and BioEngineering Abstracts
Copper Technical Reference Library
Engineered Materials Abstracts
Biotechnology Research Abstracts
Engineering Research Database
Calcium & Calcified Tissue Abstracts
Corrosion Abstracts
ANTE: Abstracts in New Technology & Engineering
Advanced Technologies Database with Aerospace
Solid State and Superconductivity Abstracts
DatabaseTitleList Technology Research Database
Materials Research Database
MEDLINE

CrossRef
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
Chemistry
Biology
EISSN 1099-1352
EndPage 400
ExternalDocumentID 3660115271
10_1002_jmr_2454
25726811
JMR2454
Genre article
Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
.3N
.GA
.GJ
.Y3
05W
0R~
10A
1L6
1OB
1OC
1ZS
31~
33P
3SF
3WU
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABPVW
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFO
ACGFS
ACIWK
ACPOU
ACPRK
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
AEEZP
AEGXH
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AFRAH
AFZJQ
AHBTC
AI.
AIAGR
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ASPBG
ATUGU
AUFTA
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BLYAC
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BY8
CS3
D-E
D-F
DCZOG
DPXWK
DR1
DR2
DRFUL
DRSTM
DU5
EBD
EBS
EJD
EMOBN
F00
F01
F04
F5P
FEDTE
G-S
G.N
GNP
GODZA
H.T
H.X
HBH
HF~
HGLYW
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LH6
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NDZJH
NF~
NNB
O66
O9-
OIG
P2P
P2W
P2X
P4D
PALCI
Q.N
Q11
QB0
QRW
R.K
RBB
RIWAO
RJQFR
ROL
RWI
RX1
RYL
SAMSI
SUPJJ
SV3
UB1
V8K
VH1
W8V
W99
WBFHL
WBKPD
WH7
WIB
WIH
WIK
WJL
WOHZO
WQJ
WRC
WSB
WXSBR
WYISQ
XG1
XV2
ZZTAW
~IA
~WT
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7QF
7QO
7QP
7QQ
7SE
7SR
7TA
7TK
7TM
8BQ
8FD
F28
FR3
H8G
JG9
P64
7U5
L7M
ID FETCH-LOGICAL-c2974-6ff7fdf5542937c941b9185a31ca3d85dd65a847ac930b793640d0f4bee596d3
IEDL.DBID DR2
ISSN 0952-3499
IngestDate Sat Aug 17 02:34:41 EDT 2024
Thu Oct 10 20:03:41 EDT 2024
Fri Aug 23 01:30:47 EDT 2024
Sat Sep 28 08:04:58 EDT 2024
Sat Aug 24 00:49:57 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords NMR
antibodies
epitope mapping
Language English
License Copyright © 2015 John Wiley & Sons, Ltd.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c2974-6ff7fdf5542937c941b9185a31ca3d85dd65a847ac930b793640d0f4bee596d3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 25726811
PQID 1674419067
PQPubID 2034569
PageCount 8
ParticipantIDs proquest_miscellaneous_1685802013
proquest_journals_1674419067
crossref_primary_10_1002_jmr_2454
pubmed_primary_25726811
wiley_primary_10_1002_jmr_2454_JMR2454
PublicationCentury 2000
PublicationDate June 2015
2015-Jun
2015-06-00
20150601
PublicationDateYYYYMMDD 2015-06-01
PublicationDate_xml – month: 06
  year: 2015
  text: June 2015
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
– name: Nutley
PublicationTitle Journal of molecular recognition
PublicationTitleAlternate J Mol Recognit
PublicationYear 2015
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 1991; 252
2007; 104
2005; 173
2011b; 213
2010; 18
2000; 8
2013; 425
2000; 7
2008; 36
1988; 242
1980; 70
2011; 12
2013; 8
2012; 447
2011; 18
1993; 3
1994; 62
2012; 30
1999; 9
2011a; 213
2001; 276
2004; 30
2004; 138
2013; 14
2010; 46
2002; 41
1990; 29
2013; 73
1997; 36
2014; 78C
2010; 132
2010; 396
2009; 284
2013
2003; 125
2008; 375
2010; 5
1994; 2
2003; 42
2009; 389
2003; 43
2007; 69
2007; 25
e_1_2_7_6_1
e_1_2_7_5_1
e_1_2_7_4_1
e_1_2_7_3_1
e_1_2_7_9_1
e_1_2_7_7_1
e_1_2_7_19_1
e_1_2_7_18_1
e_1_2_7_17_1
e_1_2_7_16_1
e_1_2_7_40_1
e_1_2_7_2_1
e_1_2_7_15_1
e_1_2_7_41_1
e_1_2_7_14_1
e_1_2_7_42_1
e_1_2_7_13_1
e_1_2_7_43_1
e_1_2_7_12_1
e_1_2_7_44_1
e_1_2_7_11_1
e_1_2_7_10_1
e_1_2_7_26_1
e_1_2_7_27_1
e_1_2_7_28_1
e_1_2_7_29_1
e_1_2_7_30_1
e_1_2_7_25_1
e_1_2_7_31_1
e_1_2_7_24_1
e_1_2_7_32_1
e_1_2_7_23_1
e_1_2_7_33_1
e_1_2_7_22_1
e_1_2_7_34_1
e_1_2_7_21_1
e_1_2_7_35_1
e_1_2_7_20_1
Corti D (e_1_2_7_8_1) 2013
Ulrich EL (e_1_2_7_36_1) 2008; 36
e_1_2_7_37_1
e_1_2_7_38_1
e_1_2_7_39_1
References_xml – volume: 73
  start-page: 1
  year: 2013
  end-page: 16
  article-title: Using chemical shift perturbation to characterise ligand binding
  publication-title: Prog. Nucl. Magn. Reson. Spectrosc.
– volume: 8
  start-page: 385
  issue: 4
  year: 2000
  end-page: 395
  article-title: NMR structure of an anti‐gp120 antibody complex with a V3 peptide reveals a surface important for co‐receptor binding
  publication-title: Structure
– volume: 252
  start-page: 1390
  issue: 5011
  year: 1991
  end-page: 1399
  article-title: Structures of larger proteins in solution: three‐ and four‐dimensional heteronuclear NMR spectroscopy
  publication-title: Science
– volume: 78C
  start-page: 47
  year: 2014
  end-page: 75
  article-title: Practical aspects of NMR signal assignment in larger and challenging proteins
  publication-title: Prog. Nucl. Magn. Reson. Spectrosc.
– volume: 125
  start-page: 1731
  issue: 7
  year: 2003
  end-page: 1737
  article-title: HADDOCK: a protein–protein docking approach based on biochemical or biophysical information
  publication-title: J. Am. Chem. Soc.
– volume: 2
  start-page: 61
  issue: 1
  year: 1994
  end-page: 93
  article-title: Resonance assignment strategies for the analysis of NMR spectra of proteins
  publication-title: Mol. Biotechnol.
– volume: 43
  start-page: 63
  year: 2003
  end-page: 103
  article-title: Chemical exchange in NMR
  publication-title: Progr. Nucl. Magn. Reson.
– volume: 42
  start-page: 14293
  issue: 48
  year: 2003
  end-page: 14305
  article-title: Epitope mapping of antigenic MUC1 peptides to breast cancer antibody fragment B27.29: a heteronuclear NMR study
  publication-title: Biochemistry
– volume: 18
  start-page: 1011
  issue: 8
  year: 2010
  end-page: 1021
  article-title: Mapping the interactions between a major pollen allergen and human IgE antibodies
  publication-title: Structure
– volume: 5
  start-page: 883
  issue: 5
  year: 2010
  end-page: 897
  article-title: The HADDOCK web server for data‐driven biomolecular docking
  publication-title: Nat. Protoc.
– volume: 18
  start-page: 347
  issue: 3
  year: 2011
  end-page: 363
  article-title: Towards fully automated structure‐based NMR resonance assignment of (1)(5)N‐labeled proteins from automatically picked peaks
  publication-title: J. Comput. Biol.
– volume: 30
  start-page: 11
  year: 2004
  end-page: 23
  article-title: Mars ‐robust automatic backbone assignment of proteins
  publication-title: J. Biomol. NMR
– volume: 41
  start-page: 1
  issue: 1
  year: 2002
  end-page: 7
  article-title: Mapping protein–protein interactions in solution by NMR spectroscopy
  publication-title: Biochemistry
– volume: 425
  start-page: 94
  issue: 1
  year: 2013
  end-page: 111
  article-title: One target‐two different binding modes: structural insights into gevokizumab and canakinumab interactions to interleukin‐1beta
  publication-title: J. Mol. Biol.
– volume: 70
  start-page: 142
  issue: A
  year: 1980
  end-page: 150
  article-title: Preparation of Fab fragments from IgGs of different animal species
  publication-title: Methods Enzymol.
– volume: 25
  start-page: 1421
  issue: 12
  year: 2007
  end-page: 1434
  article-title: The growth and potential of human antiviral monoclonal antibody therapeutics
  publication-title: Nat. Biotechnol.
– volume: 9
  start-page: 594
  issue: 5
  year: 1999
  end-page: 601
  article-title: NMR spectroscopy of large molecules and multimolecular assemblies in solution
  publication-title: Curr. Opin. Struct. Biol.
– volume: 389
  start-page: 365
  issue: 2
  year: 2009
  end-page: 375
  article-title: Efficient recovery of high‐affinity antibodies from a single‐chain Fab yeast display library
  publication-title: J. Mol. Biol.
– volume: 3
  start-page: 375
  issue: 4
  year: 1993
  end-page: 385
  article-title: Prospects for NMR of large proteins
  publication-title: J. Biomol. NMR
– volume: 30
  start-page: 615
  issue: 7
  year: 2012
  end-page: 618
  article-title: Antibody specification beyond the target: claiming a later‐generation therapeutic antibody by its target epitope
  publication-title: Nat. Biotechnol.
– volume: 375
  start-page: 151
  issue: 1
  year: 2008
  end-page: 164
  article-title: Improved segmental isotope labeling methods for the NMR study of multidomain or large proteins: application to the RRMs of Npl3p and hnRNP L
  publication-title: J. Mol. Biol.
– volume: 62
  start-page: 153
  issue: 2
  year: 1994
  end-page: 184
  article-title: Structures of larger proteins, protein–ligand and protein–DNA complexes by multi‐dimensional heteronuclear NMR
  publication-title: Prog. Biophys. Mol. Biol.
– volume: 36
  start-page: D402
  issue: Database issue
  year: 2008
  end-page: 408
  article-title: BioMagResBank
  publication-title: Nucleic Acids Res.
– volume: 14
  start-page: 457
  issue: 4
  year: 2013
  end-page: 466
  article-title: Amino acid‐selective segmental isotope labeling of multidomain proteins for structural biology
  publication-title: Chembiochem
– volume: 396
  start-page: 1491
  issue: 5
  year: 2010
  end-page: 1507
  article-title: Rapid structural characterization of human antibody–antigen complexes through experimentally validated computational docking
  publication-title: J. Mol. Biol.
– volume: 104
  start-page: 13080
  issue: 32
  year: 2007
  end-page: 13085
  article-title: Solution mapping of T cell receptor docking footprints on peptide‐MHC
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
– volume: 213
  start-page: 477
  issue: 2
  year: 2011b
  end-page: 491
  article-title: NMR studies of protein structure and dynamics. 2005
  publication-title: J. Magn. Reson.
– volume: 213
  start-page: 492
  issue: 2
  year: 2011a
  end-page: 494
  article-title: NMR studies of protein structure and dynamics ‐ a look backwards and forwards
  publication-title: J. Magn. Reson.
– volume: 132
  start-page: 5987
  issue: 17
  year: 2010
  end-page: 5989
  article-title: Direct use of N relaxation rates as experimental restraints on molecular shape and orientation for docking of protein–protein complexes
  publication-title: J. Am. Chem. Soc.
– volume: 36
  start-page: 13882
  issue: 45
  year: 1997
  end-page: 13889
  article-title: Mapping the binding site for matrix metalloproteinase on the N‐terminal domain of the tissue inhibitor of metalloproteinases‐2 by NMR chemical shift perturbation
  publication-title: Biochemistry
– volume: 46
  start-page: 51
  issue: 1
  year: 2010
  end-page: 65
  article-title: Recent advances in segmental isotope labeling of proteins: NMR applications to large proteins and glycoproteins
  publication-title: J. Biomol. NMR
– volume: 29
  start-page: 4659
  issue: 19
  year: 1990
  end-page: 4667
  article-title: A novel approach for sequential assignment of H, C, and N spectra of proteins: heteronuclear triple‐resonance three‐dimensional NMR spectroscopy. Application to calmodulin
  publication-title: Biochemistry
– volume: 284
  start-page: 31928
  issue: 46
  year: 2009
  end-page: 31935
  article-title: High resolution NMR‐based model for the structure of a scFv‐IL‐1 complex: potential for NMR as a key tool in therapeutic antibody design and development
  publication-title: J Biol Chem
– start-page: 31
  year: 2013
  article-title: Broadly neutralizing antiviral antibodies
  publication-title: Annu Rev Immunol
– volume: 173
  start-page: 193
  issue: 2
  year: 2005
  end-page: 207
  article-title: NMR studies of protein structure and dynamics
  publication-title: J. Magn. Reson.
– volume: 138
  start-page: 29
  issue: 1
  year: 2004
  end-page: 36
  article-title: Malaria parasite‐inhibitory antibody epitopes on Plasmodium falciparum merozoite surface protein‐1(19) mapped by TROSY NMR
  publication-title: Mol. Biochem. Parasitol.
– volume: 276
  start-page: 9359
  issue: 12
  year: 2001
  end-page: 9365
  article-title: Hydrogen exchange nuclear magnetic resonance spectroscopy mapping of antibody epitopes on the house dust mite allergen Der p 2
  publication-title: J. Biol. Chem.
– volume: 7
  start-page: 220
  issue: 3
  year: 2000
  end-page: 223
  article-title: A novel NMR method for determining the interfaces of large protein–protein complexes
  publication-title: Nat. Struct. Biol.
– volume: 242
  start-page: 423
  issue: 4877
  year: 1988
  end-page: 426
  article-title: Single‐chain antigen‐binding proteins
  publication-title: Science
– volume: 447
  start-page: 205
  issue: 2
  year: 2012
  end-page: 215
  article-title: Molecular structure of human GM‐CSF in complex with a disease‐associated anti‐human GM‐CSF autoantibody and its potential biological implications
  publication-title: Biochem. J.
– volume: 12
  start-page: 226
  issue: 1
  year: 2011
  end-page: 251
  article-title: Computational docking of antibody–antigen complexes, opportunities and pitfalls illustrated by influenza hemagglutinin
  publication-title: Int. J. Mol. Sci.
– volume: 69
  start-page: 726
  issue: 4
  year: 2007
  end-page: 733
  article-title: HADDOCK versus HADDOCK: new features and performance of HADDOCK2.0 on the CAPRI targets
  publication-title: Proteins
– volume: 8
  start-page: e55561
  issue: 2
  year: 2013
  article-title: Rational engineering of a human anti‐dengue antibody through experimentally validated computational docking
  publication-title: PLoS One
– ident: e_1_2_7_4_1
  doi: 10.1016/j.jmb.2012.09.021
– ident: e_1_2_7_38_1
  doi: 10.1007/BF00176005
– ident: e_1_2_7_12_1
  doi: 10.1016/j.pnmrs.2013.12.001
– ident: e_1_2_7_13_1
  doi: 10.1021/bi0301237
– ident: e_1_2_7_24_1
  doi: 10.1016/j.molbiopara.2004.06.014
– ident: e_1_2_7_3_1
  doi: 10.1126/science.3140379
– volume: 36
  start-page: D402
  year: 2008
  ident: e_1_2_7_36_1
  article-title: BioMagResBank
  publication-title: Nucleic Acids Res.
  doi: 10.1093/nar/gkm957
  contributor:
    fullname: Ulrich EL
– ident: e_1_2_7_5_1
  doi: 10.1042/BJ20120884
– ident: e_1_2_7_39_1
  doi: 10.1016/j.jmb.2009.04.019
– ident: e_1_2_7_11_1
  doi: 10.1021/ja026939x
– ident: e_1_2_7_32_1
  doi: 10.1016/j.jmb.2007.09.030
– ident: e_1_2_7_40_1
  doi: 10.1016/S0959-440X(99)00011-1
– ident: e_1_2_7_43_1
  doi: 10.1021/bi9712091
– ident: e_1_2_7_18_1
  doi: 10.1016/j.jmr.2011.08.010
– ident: e_1_2_7_7_1
  doi: 10.1016/0079-6107(94)90010-8
– ident: e_1_2_7_33_1
  doi: 10.1007/s10858-009-9362-7
– ident: e_1_2_7_25_1
  doi: 10.1074/jbc.M010812200
– ident: e_1_2_7_29_1
  doi: 10.1038/nbt.2291
– ident: e_1_2_7_23_1
  doi: 10.1002/cbic.201200732
– ident: e_1_2_7_20_1
  doi: 10.1007/BF02789290
– ident: e_1_2_7_27_1
  doi: 10.1016/j.str.2010.05.012
– ident: e_1_2_7_9_1
  doi: 10.1038/nprot.2010.32
– ident: e_1_2_7_6_1
  doi: 10.1126/science.2047852
– ident: e_1_2_7_14_1
  doi: 10.1021/bi00471a022
– ident: e_1_2_7_21_1
  doi: 10.1016/S0076-6879(80)70045-9
– ident: e_1_2_7_30_1
  doi: 10.1016/j.jmb.2009.12.053
– ident: e_1_2_7_10_1
  doi: 10.1002/prot.21723
– ident: e_1_2_7_17_1
  doi: 10.1016/j.jmr.2004.11.021
– ident: e_1_2_7_19_1
  doi: 10.1016/j.jmr.2011.09.009
– ident: e_1_2_7_28_1
  doi: 10.1021/ja101842n
– ident: e_1_2_7_2_1
  doi: 10.1016/j.pnmrs.2003.08.001
– ident: e_1_2_7_41_1
  doi: 10.1074/jbc.M109.025304
– start-page: 31
  year: 2013
  ident: e_1_2_7_8_1
  article-title: Broadly neutralizing antiviral antibodies
  publication-title: Annu Rev Immunol
  contributor:
    fullname: Corti D
– ident: e_1_2_7_34_1
  doi: 10.1038/73331
– ident: e_1_2_7_16_1
  doi: 10.1023/B:JNMR.0000042954.99056.ad
– ident: e_1_2_7_35_1
  doi: 10.1016/S0969-2126(00)00119-2
– ident: e_1_2_7_42_1
  doi: 10.1016/j.pnmrs.2013.02.001
– ident: e_1_2_7_22_1
  doi: 10.1038/nbt1363
– ident: e_1_2_7_37_1
  doi: 10.1073/pnas.0703702104
– ident: e_1_2_7_26_1
  doi: 10.3390/ijms12010226
– ident: e_1_2_7_15_1
  doi: 10.1089/cmb.2010.0251
– ident: e_1_2_7_44_1
  doi: 10.1021/bi011870b
– ident: e_1_2_7_31_1
  doi: 10.1371/journal.pone.0055561
SSID ssj0009950
Score 2.3256264
Snippet Antibodies play an ever more prominent role in basic research as well as in the biotechnology and pharmaceutical sectors. Characterizing their epitopes, that...
SourceID proquest
crossref
pubmed
wiley
SourceType Aggregation Database
Index Database
Publisher
StartPage 393
SubjectTerms Allosteric Regulation
Antibodies
Antibodies - chemistry
Antigens
Biotechnology
epitope mapping
Epitope Mapping - methods
Epitopes - chemistry
Magnetic Resonance Spectroscopy
Mapping
NMR
NMR spectroscopy
Nuclear magnetic resonance
Recognition
Residues
Solutions
Title Epitope mapping by solution NMR spectroscopy
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmr.2454
https://www.ncbi.nlm.nih.gov/pubmed/25726811
https://www.proquest.com/docview/1674419067
https://search.proquest.com/docview/1685802013
Volume 28
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bS8MwFD6IIPriZd6mUyKIT3a2TdI2j_MyxmA-DAXBh9IkraCsG7s8zF_vOe06URHEpxaaNm3O7Ut68h2Ac-LEIqo9xzORdURoXCcyynWUFZFWQnJTsn3eB51H0X2ST4usStoLU_JDLBfcyDIKf00GnujJ1Sdp6Otg3PSFJCpQj4eUzXXb_2SOUqoozooAwnc4ovqKd9b1r6obv0aiH_DyK1otwk17C56rFy2zTN6as6lumvdvHI7_-5Jt2FygUNYq1WYHVtK8BrutHGfggzm7YEVeaLHgXoO16-ps_aaqDrcLl3cj9AWjlA0SYnh4YXrOKjVm970-K7ZwElXmcDTfg4f23cNNx1lUXnCMjxMMJ8iyMLOZpGJWPDRKeFphYE-4ZxJuI2ltIBOMa4lR3NVo4oFwrZsJnaZSBZbvw2o-zNNDYJzrJLAEQtNIeBaDn69siDAkzHyhRViHs0oI8ajk14hLJmU_xnGJaVzq0KikEy8sbBLT7gmBaCagRywv4yDQD48kT4czahPJCPGwx-twUEp12Qm6Kj-IPK8OF4Vsfu097vb6dDz6a8Nj2MAuZZlP1oDV6XiWniBymerTQkc_AFh15nY
link.rule.ids 315,783,787,1378,27938,27939,46308,46732
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bS8MwFD54QfTF-2VeI4hPdrZN0jb4NHUyL9vDmOCDUJqkFZR1Q7eH-es9aZeJiiA-tdC0ac8l50t68h2AI8OJZaj2HE9F2mGhcp1ICdcRmkVSME5VyfbZChr37OaBP0zBmd0LU_JDTBbcjGcU47VxcLMgffrJGvrcfa36jLNpmEVvp6Z8wWX7kztKiKI8K0II36GI6y3zrOuf2ju_xqIfAPMrXi0CztUSPNpXLfNMXqrDgayq928sjv_8lmVYHANRUistZwWm0nwV1mo5TsK7I3JMitTQYs19FebO7dn8hS0QtwYn9T4OB_2UdBND8vBE5IhYSyatZpsUuzgNW2avP1qHzlW9c9FwxsUXHOXjHMMJsizMdMZNPSsaKsE8KTC2J9RTCdUR1zrgCYa2RAnqSvTygLnazZhMUy4CTTdgJu_l6RYQSmUSaIND04h5GuOfL3SISCTMfCZZWIFDq4W4X1JsxCWZsh-jXGIjlwrsWvXEYyd7i80GCoaAJjCPmFxGIZh_Hkme9oamTcQjhMQercBmqdZJJzha-UHkeRU4LpTza-_xTbNtjtt_bXgA841O8y6-u27d7sACds_L9LJdmBm8DtM9BDIDuV8Y7AfGmOqQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1JS8NAFH644HJxX-o6gngybZJZkjm6FdciRUHwEDIziaA0Ddoe6q_3TdJUVATxlEAmmWTe9s3kzfcA9i0nlqXaczwdGocF2nVCLV1HGhYqyTjVJdtnS5zfs8sH_jDMqrR7YUp-iNGCm7WMwl9bA89N2vgkDX3uvNZ9xtk4TDJBXZvOddr-pI6SsqjOigjCdyjC-op41vUb1Z1fQ9EPfPkVrhbxpjkPj9WblmkmL_V-T9X1-zcSx_99ygLMDWEoOSr1ZhHGkmwJlo8ynIJ3BuSAFImhxYr7EkwdV2czJ1V5uGU4PMvRGeQJ6cSW4uGJqAGp9Ji0btqk2MNpuTK7-WAF7ppndyfnzrD0gqN9nGE4Ik2D1KTcVrOigZbMUxIje0w9HVMTcmMEjzGwxVpSV6GNC-YaN2UqSbgUhq7CRNbNknUglKpYGItCk5B5BqOfL02AOCRIfaZYUIO9SghRXhJsRCWVsh_huER2XGqwVUknGprYW2S3TzCEM8I-YnQZB8H-8YizpNu3bUIeIiD2aA3WSqmOOkFf5YvQ82pwUMjm196jy5u2PW78teEuTN-eNqPri9bVJsxi77zMLduCid5rP9lGFNNTO4W6fgAXc-k_
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=Epitope+mapping+by+solution+NMR+spectroscopy&rft.jtitle=Journal+of+molecular+recognition&rft.au=Bardelli%2C+M&rft.au=Livoti%2C+E&rft.au=Simonelli%2C+L&rft.au=Pedotti%2C+M&rft.date=2015-06-01&rft.pub=Wiley+Subscription+Services%2C+Inc&rft.issn=0952-3499&rft.eissn=1099-1352&rft.volume=28&rft.issue=6&rft.spage=393&rft_id=info:doi/10.1002%2Fjmr.2454&rft.externalDBID=NO_FULL_TEXT&rft.externalDocID=3660115271
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0952-3499&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0952-3499&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0952-3499&client=summon