Visualizing Protein Interactions and Dynamics: Evolving a Visual Language for Molecular Animation
Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include protein conformational change and stability, diffusion and random molecular motion, and molecular crowding. In this study, we examined the relat...
Saved in:
Published in | CBE life sciences education Vol. 11; no. 1; pp. 103 - 110 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Cell Biology
01.03.2012
|
Subjects | |
Online Access | Get full text |
ISSN | 1931-7913 1931-7913 |
DOI | 10.1187/cbe.11-08-0071 |
Cover
Loading…
Abstract | Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include protein conformational change and stability, diffusion and random molecular motion, and molecular crowding. In this study, we examined the relative effectiveness of three-dimensional visualization techniques for learning about protein conformation and molecular motion in association with a ligand–receptor binding event. Increasingly complex versions of the same binding event were depicted in each of four animated treatments. Students (n = 131) were recruited from the undergraduate biology program at University of Toronto, Mississauga. Visualization media were developed in the Center for Molecular and Cellular Dynamics at Harvard Medical School. Stem cell factor ligand and cKit receptor tyrosine kinase were used as a classical example of a ligand-induced receptor dimerization and activation event. Each group completed a pretest, viewed one of four variants of the animation, and completed a posttest and, at 2 wk following the assessment, a delayed posttest. Overall, the most complex animation was the most effective at fostering students' understanding of the events depicted. These results suggest that, in select learning contexts, increasingly complex representations may be more desirable for conveying the dynamic nature of cell binding events. |
---|---|
AbstractList | Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include protein conformational change and stability, diffusion and random molecular motion, and molecular crowding. In this study, we examined the relative effectiveness of three-dimensional visualization techniques for learning about protein conformation and molecular motion in association with a ligand–receptor binding event. Increasingly complex versions of the same binding event were depicted in each of four animated treatments. Students (n = 131) were recruited from the undergraduate biology program at University of Toronto, Mississauga. Visualization media were developed in the Center for Molecular and Cellular Dynamics at Harvard Medical School. Stem cell factor ligand and cKit receptor tyrosine kinase were used as a classical example of a ligand-induced receptor dimerization and activation event. Each group completed a pretest, viewed one of four variants of the animation, and completed a posttest and, at 2 wk following the assessment, a delayed posttest. Overall, the most complex animation was the most effective at fostering students' understanding of the events depicted. These results suggest that, in select learning contexts, increasingly complex representations may be more desirable for conveying the dynamic nature of cell binding events. Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include protein conformational change and stability, diffusion and random molecular motion, and molecular crowding. In this study, we examined the relative effectiveness of three-dimensional visualization techniques for learning about protein conformation and molecular motion in association with a ligand–receptor binding event. Increasingly complex versions of the same binding event were depicted in each of four animated treatments. Students ( n = 131) were recruited from the undergraduate biology program at University of Toronto, Mississauga. Visualization media were developed in the Center for Molecular and Cellular Dynamics at Harvard Medical School. Stem cell factor ligand and cKit receptor tyrosine kinase were used as a classical example of a ligand-induced receptor dimerization and activation event. Each group completed a pretest, viewed one of four variants of the animation, and completed a posttest and, at 2 wk following the assessment, a delayed posttest. Overall, the most complex animation was the most effective at fostering students' understanding of the events depicted. These results suggest that, in select learning contexts, increasingly complex representations may be more desirable for conveying the dynamic nature of cell binding events. Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include protein conformational change and stability, diffusion and random molecular motion, and molecular crowding. In this study, we examined the relative effectiveness of three-dimensional visualization techniques for learning about protein conformation and molecular motion in association with a ligand-receptor binding event. Increasingly complex versions of the same binding event were depicted in each of four animated treatments. Students (n = 131) were recruited from the undergraduate biology program at University of Toronto, Mississauga. Visualization media were developed in the Center for Molecular and Cellular Dynamics at Harvard Medical School. Stem cell factor ligand and cKit receptor tyrosine kinase were used as a classical example of a ligand-induced receptor dimerization and activation event. Each group completed a pretest, viewed one of four variants of the animation, and completed a posttest and, at 2 wk following the assessment, a delayed posttest. Overall, the most complex animation was the most effective at fostering students' understanding of the events depicted. These results suggest that, in select learning contexts, increasingly complex representations may be more desirable for conveying the dynamic nature of cell binding events.Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include protein conformational change and stability, diffusion and random molecular motion, and molecular crowding. In this study, we examined the relative effectiveness of three-dimensional visualization techniques for learning about protein conformation and molecular motion in association with a ligand-receptor binding event. Increasingly complex versions of the same binding event were depicted in each of four animated treatments. Students (n = 131) were recruited from the undergraduate biology program at University of Toronto, Mississauga. Visualization media were developed in the Center for Molecular and Cellular Dynamics at Harvard Medical School. Stem cell factor ligand and cKit receptor tyrosine kinase were used as a classical example of a ligand-induced receptor dimerization and activation event. Each group completed a pretest, viewed one of four variants of the animation, and completed a posttest and, at 2 wk following the assessment, a delayed posttest. Overall, the most complex animation was the most effective at fostering students' understanding of the events depicted. These results suggest that, in select learning contexts, increasingly complex representations may be more desirable for conveying the dynamic nature of cell binding events. Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include protein conformational change and stability, diffusion and random molecular motion, and molecular crowding. In this study, we examined the relative effectiveness of three-dimensional visualization techniques for learning about protein conformation and molecular motion in association with a ligand-receptor binding event. Increasingly complex versions of the same binding event were depicted in each of four animated treatments. Students (n = 131) were recruited from the undergraduate biology program at University of Toronto, Mississauga. Visualization media were developed in the Center for Molecular and Cellular Dynamics at Harvard Medical School. Stem cell factor ligand and cKit receptor tyrosine kinase were used as a classical example of a ligand-induced receptor dimerization and activation event. Each group completed a pretest, viewed one of four variants of the animation, and completed a posttest and, at 2 wk following the assessment, a delayed posttest. Overall, the most complex animation was the most effective at fostering students' understanding of the events depicted. These results suggest that, in select learning contexts, increasingly complex representations may be more desirable for conveying the dynamic nature of cell binding events. (Contains 5 tables and 4 figures.) |
Audience | Higher Education |
Author | Jodie Jenkinson Gaël McGill |
Author_xml | – sequence: 1 givenname: Jodie surname: Jenkinson fullname: Jenkinson, Jodie organization: Biomedical Communications Program, Department of Biology, University of Toronto, Mississauga, Mississauga, Ontario L5L 1C6, Canada – sequence: 2 givenname: Gaël surname: McGill fullname: McGill, Gaël organization: Department of Biological Chemistry and Molecular Pharmacology, Center for Molecular and Cellular Dynamics, Harvard Medical School, Boston, MA 02115 |
BackLink | http://eric.ed.gov/ERICWebPortal/detail?accno=EJ969266$$DView record in ERIC https://www.ncbi.nlm.nih.gov/pubmed/22383622$$D View this record in MEDLINE/PubMed |
BookMark | eNp1UUtv1DAQtlARfcCVE0K-oJ5S_EhihwNSVRYoWgQH4GpNHCdr5NjFTnbV_nq8pK0KEvLBI32P-WbmGB344A1Czyk5o1SK17o1uSiILAgR9BE6og2nhWgoP3hQH6LjlH4SUtaEVk_QIWNc8pqxIwQ_bJrB2RvrB_w1hslYjy_9ZCLoyQafMPgOv7v2MFqd3uDVNrjtngt4UeI1-GGGweA-RPw5OKNnBxGfezvC3uEpetyDS-bZ7X-Cvr9ffbv4WKy_fLi8OF8XuizJVIgWuOg05Vr2gnZU1pIwwaWkjGvoqjyGpEaanlDW0raDivRtJSQzQAVlwE_Q28X3am5H02njpwhOXcWcI16rAFb9jXi7UUPYKs4aRuomG5zeGsTwazZpUqNN2jgH3oQ5qYbVtCp5JTPz5cNW9z3u1poJLxaCiVbfw6tPTZ1N6gyXC6xjSCmaXmk7_VlWDmadokTtj6vycXOhiFT742bZ2T-yO-f_Cl4tgo0dNjsbjUojOJdTM7Xb7TIzP8L5b2gns9E |
CitedBy_id | crossref_primary_10_1080_15551393_2016_1178582 crossref_primary_10_3390_educsci14040366 crossref_primary_10_1002_bmb_20737 crossref_primary_10_1002_bmb_20956 crossref_primary_10_1111_cgf_14575 crossref_primary_10_1187_cbe_16_03_0141 crossref_primary_10_1111_cgf_14836 crossref_primary_10_1080_17453054_2019_1671814 crossref_primary_10_7554_eLife_64047 crossref_primary_10_1525_abt_2015_77_6_463 crossref_primary_10_1525_abt_2022_84_6_328 crossref_primary_10_3389_fmicb_2021_643951 crossref_primary_10_1002_bmb_21575 crossref_primary_10_1002_bmb_21076 crossref_primary_10_1039_C4FD00014E crossref_primary_10_1187_cbe_17_12_0267 crossref_primary_10_1186_s43031_019_0016_7 crossref_primary_10_3389_fbinf_2024_1353807 crossref_primary_10_1002_bmb_20943 crossref_primary_10_1002_bmb_20940 crossref_primary_10_1080_17453054_2018_1490892 crossref_primary_10_1187_cbe_13_01_0014 crossref_primary_10_1021_acs_jchemed_9b01161 crossref_primary_10_1021_ed400201v crossref_primary_10_1515_jib_2022_0016 crossref_primary_10_1016_j_jmb_2019_02_018 crossref_primary_10_1016_j_jmb_2018_08_020 crossref_primary_10_1371_journal_pone_0293592 crossref_primary_10_1088_1742_6596_1796_1_012066 crossref_primary_10_1097_CIN_0000000000000038 crossref_primary_10_1187_cbe_19_11_0254 crossref_primary_10_1126_science_1220252 crossref_primary_10_1002_sce_21215 crossref_primary_10_1109_TVCG_2014_2346352 |
Cites_doi | 10.1080/09500690305017 10.1016/j.cell.2008.06.013 10.1894/0038-4909(2006)68[299:TIP]2.0.CO;2 10.1016/j.tcb.2010.08.005 10.1016/S0959-4752(02)00018-X 10.1187/cbe.08-07-0039 10.1016/j.str.2010.12.023 10.1006/ijhc.2002.1017 10.1187/cbe.10-03-0044 10.1187/cbe.07-01-0002 10.1187/cbe.05-02-0068 10.1187/cbe.07-08-0063 10.1187/cbe.10-01-0001 10.1187/cbe.10-03-0018 10.1007/BF03172967 10.1002/bmb.2006.49403402094 10.1016/j.cell.2007.05.055 10.1187/cbe.08-09-0055 10.1016/S0968-0004(01)01938-7 10.1187/cbe.09-12-0092 |
ContentType | Journal Article |
Copyright | 2012 J. Jenkinson and G. McGill. © 2012 The American Society for Cell Biology. This article is distributed by The American Society for Cell Biology under license from the author(s). It is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License ( ). 2012 |
Copyright_xml | – notice: 2012 J. Jenkinson and G. McGill. © 2012 The American Society for Cell Biology. This article is distributed by The American Society for Cell Biology under license from the author(s). It is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License ( ). 2012 |
DBID | AAYXX CITATION 7SW BJH BNH BNI BNJ BNO ERI PET REK WWN CGR CUY CVF ECM EIF NPM 7X8 5PM |
DOI | 10.1187/cbe.11-08-0071 |
DatabaseName | CrossRef ERIC ERIC (Ovid) ERIC ERIC ERIC (Legacy Platform) ERIC( SilverPlatter ) ERIC ERIC PlusText (Legacy Platform) Education Resources Information Center (ERIC) ERIC Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef ERIC MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | CrossRef MEDLINE MEDLINE - Academic ERIC |
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 – sequence: 3 dbid: ERI name: ERIC url: https://eric.ed.gov/ sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1931-7913 |
ERIC | EJ969266 |
EndPage | 110 |
ExternalDocumentID | PMC3292069 22383622 EJ969266 10_1187_cbe_11_08_0071 www11_1_103 |
Genre | Research Support, U.S. Gov't, Non-P.H.S Journal Article |
GeographicLocations | Canada |
GeographicLocations_xml | – name: Canada |
GroupedDBID | - 29B 2WC 53G 5GY 6~0 6~1 ABSGY ADACO ADBBV AENEX ALMA_UNASSIGNED_HOLDINGS BAWUL DIK E3Z EBS EE- F5P GX1 H13 HYE INIJC LI0 M~E R0Z RHF RNS RPM TCB WOQ --- 18M 6J9 AAYXX ABOPQ ABSQV AIPOO AOIJS C1A CITATION EJD EMOBN F9R IAO IER IGS ITC OVT W8F ZBA 7SW BJH BNH BNI BNJ BNO ERI PET REK WWN CGR CUY CVF ECM EIF NPM 7X8 5PM |
ID | FETCH-LOGICAL-c440t-7ba37dc13c8f71d1868027388123cad579181e8ef012b1bda50fb5782ea1712a3 |
ISSN | 1931-7913 |
IngestDate | Thu Aug 21 18:16:29 EDT 2025 Sun Aug 24 04:13:41 EDT 2025 Mon Jul 21 05:34:22 EDT 2025 Tue Sep 02 19:34:28 EDT 2025 Thu Apr 24 22:55:28 EDT 2025 Tue Jul 01 03:38:44 EDT 2025 Tue Jan 05 20:17:11 EST 2021 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Language | English |
License | “ASCB®” and “The American Society for Cell Biology®” are registered trademarks of The American Society of Cell Biology. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c440t-7ba37dc13c8f71d1868027388123cad579181e8ef012b1bda50fb5782ea1712a3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | https://pubmed.ncbi.nlm.nih.gov/PMC3292069 |
PMID | 22383622 |
PQID | 926154358 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_3292069 proquest_miscellaneous_926154358 pubmed_primary_22383622 eric_primary_EJ969266 crossref_citationtrail_10_1187_cbe_11_08_0071 crossref_primary_10_1187_cbe_11_08_0071 highwire_smallpub2_www11_1_103 |
ProviderPackageCode | RHF CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2012-03-01 |
PublicationDateYYYYMMDD | 2012-03-01 |
PublicationDate_xml | – month: 03 year: 2012 text: 2012-03-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | CBE life sciences education |
PublicationTitleAlternate | CBE Life Sci Educ |
PublicationYear | 2012 |
Publisher | American Society for Cell Biology |
Publisher_xml | – name: American Society for Cell Biology |
References | B21 B22 National Research Council (B20) 2009 Yuzawa S (B29) 2007; 130 B24 McGill G (B18) 2008; 133 B26 Tversky B (B27) 2002; 57 B28 Linn MC (B14) 2008 Paivio A (B21a) 1986 Andrei RM (B3) 2010 Schönborn KJ (B23) 2006; 34 Linn MC (B12) 2003; 25 Howitt S (B8) 2008; 39 B11 B15 Ellis RJ (B4) 2001; 26 Iwasa JH (B9) 2010; 20 B19 B1 B2 Tasker R (B25) 2006; 7 B6 Lowe RK (B17) 2003; 13 B7 Flannery MC (B5) 2006; 68 Linn MC (B13) 2010 Johnson GT (B10) 2011; 19 Lowe RK (B16) 1999; 14 17662946 - Cell. 2007 Jul 27;130(2):323-34 20194805 - CBE Life Sci Educ. 2010 Spring;9(1):25-33 19255134 - CBE Life Sci Educ. 2009 Spring;8(1):29-43 21123690 - CBE Life Sci Educ. 2010 Winter;9(4):435-40 18585343 - Cell. 2008 Jun 27;133(7):1127-32 21638645 - Biochem Mol Biol Educ. 2006 Mar;34(2):94-102 15917868 - Cell Biol Educ. 2005 Summer;4(2):112-7 20194802 - CBE Life Sci Educ. 2010 Spring;9(1):10-6 18519614 - CBE Life Sci Educ. 2008 Summer;7(2):227-33 20832316 - Trends Cell Biol. 2010 Dec;20(12):699-704 17785404 - CBE Life Sci Educ. 2007 Fall;6(3):217-23 22536962 - BMC Bioinformatics. 2012;13 Suppl 4:S16 20810950 - CBE Life Sci Educ. 2010 Fall;9(3):189-95 20516350 - CBE Life Sci Educ. 2010 Summer;9(2):71-3 21397181 - Structure. 2011 Mar 9;19(3):293-303 11590012 - Trends Biochem Sci. 2001 Oct;26(10):597-604 |
References_xml | – volume: 25 start-page: 727 year: 2003 ident: B12 publication-title: Int J Sci Educ doi: 10.1080/09500690305017 – volume: 133 start-page: 1127 year: 2008 ident: B18 publication-title: Cell doi: 10.1016/j.cell.2008.06.013 – start-page: 221 volume-title: Proceedings of the 8th International Conference of the Learning Sciences, part 3 year: 2008 ident: B14 – volume: 68 start-page: 299 year: 2006 ident: B5 publication-title: Am Biol Teach doi: 10.1894/0038-4909(2006)68[299:TIP]2.0.CO;2 – volume: 20 start-page: 699 year: 2010 ident: B9 publication-title: Trends Cell Biol doi: 10.1016/j.tcb.2010.08.005 – ident: B1 – volume: 13 start-page: 157 year: 2003 ident: B17 publication-title: Learn Instruct doi: 10.1016/S0959-4752(02)00018-X – ident: B7 doi: 10.1187/cbe.08-07-0039 – volume: 19 start-page: 293 year: 2011 ident: B10 publication-title: Structure doi: 10.1016/j.str.2010.12.023 – volume: 57 start-page: 247 year: 2002 ident: B27 publication-title: Int J Hum Comput Stud doi: 10.1006/ijhc.2002.1017 – ident: B28 doi: 10.1187/cbe.10-03-0044 – ident: B21 doi: 10.1187/cbe.07-01-0002 – ident: B24 doi: 10.1187/cbe.05-02-0068 – ident: B6 doi: 10.1187/cbe.07-08-0063 – start-page: 112 year: 2009 ident: B20 publication-title: A New Biology for the 21st Century: Ensuring the United States Leads the Coming Biology Revolution – ident: B19 doi: 10.1187/cbe.10-01-0001 – volume: 7 start-page: 141 year: 2006 ident: B25 publication-title: Educ Res – ident: B22 doi: 10.1187/cbe.10-03-0018 – volume: 14 start-page: 225 year: 1999 ident: B16 publication-title: Eur J Psychol Educ doi: 10.1007/BF03172967 – ident: B2 – start-page: 239 volume-title: Successful Remembering and Successful Forgetting: A Festchrift in Honor of Robert A. Bjork year: 2010 ident: B13 – volume: 39 start-page: 1 year: 2008 ident: B8 publication-title: Australian Biochemist – volume: 34 start-page: 94 year: 2006 ident: B23 publication-title: Biochem Mol Biol Educ doi: 10.1002/bmb.2006.49403402094 – volume: 130 start-page: 323 year: 2007 ident: B29 publication-title: Cell doi: 10.1016/j.cell.2007.05.055 – volume-title: BioBlender: A Software for Intuitive Representation of Surface Properties of Biomolecules year: 2010 ident: B3 – year: 1986 ident: B21a publication-title: Mental Representations: A Dual Coding Approach, Oxford, England: Oxford University Press – ident: B26 doi: 10.1187/cbe.08-09-0055 – volume: 26 start-page: 597 year: 2001 ident: B4 publication-title: Trends Biochem Sci doi: 10.1016/S0968-0004(01)01938-7 – ident: B11 doi: 10.1187/cbe.09-12-0092 – ident: B15 – reference: 20832316 - Trends Cell Biol. 2010 Dec;20(12):699-704 – reference: 21638645 - Biochem Mol Biol Educ. 2006 Mar;34(2):94-102 – reference: 21123690 - CBE Life Sci Educ. 2010 Winter;9(4):435-40 – reference: 15917868 - Cell Biol Educ. 2005 Summer;4(2):112-7 – reference: 20194802 - CBE Life Sci Educ. 2010 Spring;9(1):10-6 – reference: 11590012 - Trends Biochem Sci. 2001 Oct;26(10):597-604 – reference: 18519614 - CBE Life Sci Educ. 2008 Summer;7(2):227-33 – reference: 20810950 - CBE Life Sci Educ. 2010 Fall;9(3):189-95 – reference: 17662946 - Cell. 2007 Jul 27;130(2):323-34 – reference: 21397181 - Structure. 2011 Mar 9;19(3):293-303 – reference: 20194805 - CBE Life Sci Educ. 2010 Spring;9(1):25-33 – reference: 18585343 - Cell. 2008 Jun 27;133(7):1127-32 – reference: 17785404 - CBE Life Sci Educ. 2007 Fall;6(3):217-23 – reference: 19255134 - CBE Life Sci Educ. 2009 Spring;8(1):29-43 – reference: 20516350 - CBE Life Sci Educ. 2010 Summer;9(2):71-3 – reference: 22536962 - BMC Bioinformatics. 2012;13 Suppl 4:S16 |
SSID | ssj0046015 |
Score | 2.1091228 |
Snippet | Undergraduate biology education provides students with a number of learning challenges. Subject areas that are particularly difficult to understand include... |
SourceID | pubmedcentral proquest pubmed eric crossref highwire |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 103 |
SubjectTerms | Adolescent Animation Audiovisual Aids Biology Canada Comprehension Computer-Assisted Instruction - methods Cytology Educational Technology Educational Technology - methods Experiments Foreign Countries Humans Internet Medical Schools Molecular Biology Molecular Biology - education Motion Pretests Posttests Proteins - chemistry Science Education Science Instruction Students Undergraduate Students Visual Stimuli Visualization Young Adult |
Title | Visualizing Protein Interactions and Dynamics: Evolving a Visual Language for Molecular Animation |
URI | http://www.lifescied.org/content/11/1/103.abstract http://eric.ed.gov/ERICWebPortal/detail?accno=EJ969266 https://www.ncbi.nlm.nih.gov/pubmed/22383622 https://www.proquest.com/docview/926154358 https://pubmed.ncbi.nlm.nih.gov/PMC3292069 |
Volume | 11 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3Na9swFBdZx2CXsY9u87oFHQY7BHeWZcf2bm2WtoRl9NCO3owsy9TgOGVJCeSv73uW5NhrB1sJGONIctDvF-m9p_dByGfOZCGizHe59DI3gN_qxjwHVUXEfsG8Is49jB2e_xyfXQazq_BqMNh2o0vW2aHcPhhX8hhU4RngilGy_4FsOyg8gHvAF66AMFz_CeNf5QpjIreo7p9jwoXSmPh0tIJOv_xd15xvXN-msBg1FgQx0n1HP4y9snE3nNtauaOjulzsMLOZDI6no6os1MhsmyuT97VzlD9TWIrBRHHNlnm5c62VpyZz9qloTuePq67FAV03eM97wx4ldf1KJ2hp1OUz9RKm9HqacIYZMXlvwWX3iKVXT-bxzkbMtL_r_TUerSQnMlOH2rqLUlK3IUznzaJBHESfGDZof7fXtR6I5_MJx0Jd4-QJeeqDiuFZS4_exQNQVEOT5BNe-LX_OkwhbcbuyTPWZd6mmn5IbfnT-7Yjzly8JC-MHkKPNKlekYGqX5NnZmrfENGhFjXUol1qUaAWtdT6Ri2xqKC6J7XEooAbbYlFW2Ltk8uT6cXkzDXVOFwZBN7ajTLBo1wyLuMiYjmWWWhyIYGEyKXIQ0A5ZipWBTAmY1kuQq_IsFiCEixivuBvyV69rNV7QsVYJXkoY5hAEeSFEL5MxopDJ5T4Re4Q185pKk2qeqyYUqWNyhpHKcABNylWUAU4HPKlbX-jk7T8teU-QtS2ms6ScQIyqkOGFrN0tRBVBRD56Wazga7w8bhDqEUyhQUYT9VErZa3qxS6gxrCw9gh7zSw7eiWIw6JepC3DTC3e_-burxucrwbcn54dM8D8nz33_1I9ta_b9UnkJ_X2bCxEQ0but8BlY_LvA |
linkProvider | National Library of Medicine |
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=Visualizing+Protein+Interactions+and+Dynamics%3A+Evolving+a+Visual+Language+for+Molecular+Animation&rft.jtitle=CBE+life+sciences+education&rft.au=Jenkinson%2C+Jodie&rft.au=McGill%2C+Ga%C3%ABl&rft.date=2012-03-01&rft.pub=American+Society+for+Cell+Biology&rft.eissn=1931-7913&rft.volume=11&rft.issue=1&rft.spage=103&rft.epage=110&rft_id=info:doi/10.1187%2Fcbe.11-08-0071&rft_id=info%3Apmid%2F22383622&rft.externalDocID=PMC3292069 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1931-7913&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1931-7913&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1931-7913&client=summon |