Source:http://linkedlifedata.com/resource/pubmed/id/11340656
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2001-5-7
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pubmed:abstractText |
Molecular dynamics simulations were conducted to estimate the free energy barrier of unfolding surfactant-associated polypeptide C (SP-C) from an alpha-helical conformation. Experimental studies indicate that while the helical fold of SP-C is thermodynamically stable in phospholipid micelles, it is metastable in a mixed organic solvent of CHCl3/CH3OH/0.1 M HCl at 32:64:5 (v/v/v), in which it undergoes an irreversible transformation to an insoluble aggregate that contains beta-sheet. On the basis of experimental observations, the free energy barrier was estimated to be approximately 100 kJ/mole by applying Eyring's transition state theory to the experimental rate of unfolding [Protein Sci 1998;7:2533-2540]. These studies prompted us to carry out simulations to investigate the unwinding process of two helical turns encompassing residues 25-32 in water and in methanol. The results give an upper bound estimation for the free energy barrier of unfolding of SP-C of approximately 20 kJ/mole. The results suggest a need to reconsider the applicability of a single-mode activated process theory to protein unfolding.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Proteolipids,
http://linkedlifedata.com/resource/pubmed/chemical/Pulmonary Surfactants,
http://linkedlifedata.com/resource/pubmed/chemical/Solvents,
http://linkedlifedata.com/resource/pubmed/chemical/polypeptide C
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0887-3585
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2001 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
395-402
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11340656-Amino Acid Sequence,
pubmed-meshheading:11340656-Animals,
pubmed-meshheading:11340656-Computer Simulation,
pubmed-meshheading:11340656-Humans,
pubmed-meshheading:11340656-Models, Molecular,
pubmed-meshheading:11340656-Peptides,
pubmed-meshheading:11340656-Protein Folding,
pubmed-meshheading:11340656-Protein Structure, Secondary,
pubmed-meshheading:11340656-Proteolipids,
pubmed-meshheading:11340656-Pulmonary Surfactants,
pubmed-meshheading:11340656-Solvents,
pubmed-meshheading:11340656-Thermodynamics
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pubmed:year |
2001
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pubmed:articleTitle |
Free energy barrier estimation of unfolding the alpha-helical surfactant-associated polypeptide C.
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pubmed:affiliation |
Groningen Biomolecular Sciences and Biotechnology Institute, Department of Biophysical Chemistry, University of Groningen, Groningen, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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