Intermediates can Accelerate Protein Folding
The effect of intermediates on the rate of protein folding is explored by applying Kramers' theory of diffusive barrier crossing in the high friction limit. Intermediates are represented as local minima in the transition barrier. We observe that very large or very small additional barriers crea...
Gespeichert in:
Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1999-06, Vol.96 (12), p.6716-6721 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 6721 |
---|---|
container_issue | 12 |
container_start_page | 6716 |
container_title | Proceedings of the National Academy of Sciences - PNAS |
container_volume | 96 |
creator | Wagner, Clemens Kiephaber, Thomas |
description | The effect of intermediates on the rate of protein folding is explored by applying Kramers' theory of diffusive barrier crossing in the high friction limit. Intermediates are represented as local minima in the transition barrier. We observe that very large or very small additional barriers created by the intermediates slow down the folding process. The rate of folding markedly increases, however, when the additional barriers become >1 kBT but leave the overall barrier height unchanged. This rate-enhancing effect is caused by a favorable entropic contribution to the free energy of activation, and it increases with the number of intermediates up to a limiting value. From these calculations, we conclude that optimized transition barriers should contain partially folded high energy intermediates. |
doi_str_mv | 10.1073/pnas.96.12.6716 |
format | Article |
fullrecord | <record><control><sourceid>jstor_pnas_</sourceid><recordid>TN_cdi_pnas_primary_96_12_6716_fulltext</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>47947</jstor_id><sourcerecordid>47947</sourcerecordid><originalsourceid>FETCH-LOGICAL-c488t-12d642dea3a90562ef9dffe58431821f58ffd6e9c435aff39a099bbdeda612303</originalsourceid><addsrcrecordid>eNptkc1PGzEQxS1UBCntuRIHFPVAL90w_livLfWCUKFISPQAZ8vZHdONNnZqe1H73-MoKQ2Ik2XN7z29mUfIJwozCg0_W3mbZlrOKJvJhso9MqGgaSWFhndkAsCaSgkmDsn7lBYAoGsFB-SQAq9106gJ-XrtM8Yldr3NmKat9dPztsUBY_lPf8aQsffTyzB0vX_4QPadHRJ-3L5H5P7y-93Fj-rm9ur64vymaoVSuaKsk4J1aLnVUEuGTnfOYa0Ep4pRVyvnOom6Fby2znFtQev5vMPOSso48CPybeO7GuclWos-RzuYVeyXNv41wfbm5cT3v8xDeDSMakWL_HQrj-H3iCmbZZ_KToP1GMZkpFagJGsK-PkVuAhj9GU1w4ByWm7ECnS2gdoYUoronnNQMOsSzLoEo6WhzKxLKIqT3fg7_ObqBfiyBdbKf-P_DsaNw5DxT96xepsswPEGWKQc4jMhGi0a_gQGsaRG</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>201315972</pqid></control><display><type>article</type><title>Intermediates can Accelerate Protein Folding</title><source>Jstor Complete Legacy</source><source>MEDLINE</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Wagner, Clemens ; Kiephaber, Thomas</creator><creatorcontrib>Wagner, Clemens ; Kiephaber, Thomas</creatorcontrib><description>The effect of intermediates on the rate of protein folding is explored by applying Kramers' theory of diffusive barrier crossing in the high friction limit. Intermediates are represented as local minima in the transition barrier. We observe that very large or very small additional barriers created by the intermediates slow down the folding process. The rate of folding markedly increases, however, when the additional barriers become >1 kBT but leave the overall barrier height unchanged. This rate-enhancing effect is caused by a favorable entropic contribution to the free energy of activation, and it increases with the number of intermediates up to a limiting value. From these calculations, we conclude that optimized transition barriers should contain partially folded high energy intermediates.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.96.12.6716</identifier><identifier>PMID: 10359778</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Biological Sciences ; Coordinate systems ; Curvature ; Eigenvalues ; Energy ; Energy levels ; Entropy ; Experiments ; Humans ; Kinetics ; Local minimum ; Models, Chemical ; Molecules ; Protein Folding ; Proteins ; Proteins - chemistry ; Theory</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1999-06, Vol.96 (12), p.6716-6721</ispartof><rights>Copyright 1933-1999 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Jun 8, 1999</rights><rights>Copyright © 1999, The National Academy of Sciences 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-12d642dea3a90562ef9dffe58431821f58ffd6e9c435aff39a099bbdeda612303</citedby><cites>FETCH-LOGICAL-c488t-12d642dea3a90562ef9dffe58431821f58ffd6e9c435aff39a099bbdeda612303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/96/12.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/47947$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/47947$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10359778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wagner, Clemens</creatorcontrib><creatorcontrib>Kiephaber, Thomas</creatorcontrib><title>Intermediates can Accelerate Protein Folding</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The effect of intermediates on the rate of protein folding is explored by applying Kramers' theory of diffusive barrier crossing in the high friction limit. Intermediates are represented as local minima in the transition barrier. We observe that very large or very small additional barriers created by the intermediates slow down the folding process. The rate of folding markedly increases, however, when the additional barriers become >1 kBT but leave the overall barrier height unchanged. This rate-enhancing effect is caused by a favorable entropic contribution to the free energy of activation, and it increases with the number of intermediates up to a limiting value. From these calculations, we conclude that optimized transition barriers should contain partially folded high energy intermediates.</description><subject>Animals</subject><subject>Biological Sciences</subject><subject>Coordinate systems</subject><subject>Curvature</subject><subject>Eigenvalues</subject><subject>Energy</subject><subject>Energy levels</subject><subject>Entropy</subject><subject>Experiments</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Local minimum</subject><subject>Models, Chemical</subject><subject>Molecules</subject><subject>Protein Folding</subject><subject>Proteins</subject><subject>Proteins - chemistry</subject><subject>Theory</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc1PGzEQxS1UBCntuRIHFPVAL90w_livLfWCUKFISPQAZ8vZHdONNnZqe1H73-MoKQ2Ik2XN7z29mUfIJwozCg0_W3mbZlrOKJvJhso9MqGgaSWFhndkAsCaSgkmDsn7lBYAoGsFB-SQAq9106gJ-XrtM8Yldr3NmKat9dPztsUBY_lPf8aQsffTyzB0vX_4QPadHRJ-3L5H5P7y-93Fj-rm9ur64vymaoVSuaKsk4J1aLnVUEuGTnfOYa0Ep4pRVyvnOom6Fby2znFtQev5vMPOSso48CPybeO7GuclWos-RzuYVeyXNv41wfbm5cT3v8xDeDSMakWL_HQrj-H3iCmbZZ_KToP1GMZkpFagJGsK-PkVuAhj9GU1w4ByWm7ECnS2gdoYUoronnNQMOsSzLoEo6WhzKxLKIqT3fg7_ObqBfiyBdbKf-P_DsaNw5DxT96xepsswPEGWKQc4jMhGi0a_gQGsaRG</recordid><startdate>19990608</startdate><enddate>19990608</enddate><creator>Wagner, Clemens</creator><creator>Kiephaber, Thomas</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><general>The National Academy of Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19990608</creationdate><title>Intermediates can Accelerate Protein Folding</title><author>Wagner, Clemens ; Kiephaber, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-12d642dea3a90562ef9dffe58431821f58ffd6e9c435aff39a099bbdeda612303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological Sciences</topic><topic>Coordinate systems</topic><topic>Curvature</topic><topic>Eigenvalues</topic><topic>Energy</topic><topic>Energy levels</topic><topic>Entropy</topic><topic>Experiments</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Local minimum</topic><topic>Models, Chemical</topic><topic>Molecules</topic><topic>Protein Folding</topic><topic>Proteins</topic><topic>Proteins - chemistry</topic><topic>Theory</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wagner, Clemens</creatorcontrib><creatorcontrib>Kiephaber, Thomas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wagner, Clemens</au><au>Kiephaber, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intermediates can Accelerate Protein Folding</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1999-06-08</date><risdate>1999</risdate><volume>96</volume><issue>12</issue><spage>6716</spage><epage>6721</epage><pages>6716-6721</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The effect of intermediates on the rate of protein folding is explored by applying Kramers' theory of diffusive barrier crossing in the high friction limit. Intermediates are represented as local minima in the transition barrier. We observe that very large or very small additional barriers created by the intermediates slow down the folding process. The rate of folding markedly increases, however, when the additional barriers become >1 kBT but leave the overall barrier height unchanged. This rate-enhancing effect is caused by a favorable entropic contribution to the free energy of activation, and it increases with the number of intermediates up to a limiting value. From these calculations, we conclude that optimized transition barriers should contain partially folded high energy intermediates.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>10359778</pmid><doi>10.1073/pnas.96.12.6716</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0027-8424 |
ispartof | Proceedings of the National Academy of Sciences - PNAS, 1999-06, Vol.96 (12), p.6716-6721 |
issn | 0027-8424 1091-6490 |
language | eng |
recordid | cdi_pnas_primary_96_12_6716_fulltext |
source | Jstor Complete Legacy; MEDLINE; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Animals Biological Sciences Coordinate systems Curvature Eigenvalues Energy Energy levels Entropy Experiments Humans Kinetics Local minimum Models, Chemical Molecules Protein Folding Proteins Proteins - chemistry Theory |
title | Intermediates can Accelerate Protein Folding |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T07%3A18%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_pnas_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intermediates%20can%20Accelerate%20Protein%20Folding&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Wagner,%20Clemens&rft.date=1999-06-08&rft.volume=96&rft.issue=12&rft.spage=6716&rft.epage=6721&rft.pages=6716-6721&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.96.12.6716&rft_dat=%3Cjstor_pnas_%3E47947%3C/jstor_pnas_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=201315972&rft_id=info:pmid/10359778&rft_jstor_id=47947&rfr_iscdi=true |