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PMID: 16074985 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Missense meanderings in sequence space: a biophysical view of protein evolution.

Nature reviews. Genetics ·Vol. 6 ·No. 9 ·2005-09-00 ·Pages 678-87

DePristo MA, Weinreich DM, Hartl DL

Abstract

Proteins are finicky molecules; they are barely stable and are prone to aggregate, but they must function in a crowded environment that is full of degradative enzymes bent on their destruction. It is no surprise that many common diseases are due to missense mutations that affect protein stability and aggregation. Here we review the literature on biophysics as it relates to molecular evolution, focusing on how protein stability and aggregation affect organismal fitness. We then advance a biophysical model of protein evolution that helps us to understand phenomena that range from the dynamics of molecular adaptation to the clock-like rate of protein evolution.

MeSH Terms
Adaptation, Biological/genetics Biophysical Phenomena Biophysics DNA/genetics Evolution, Molecular Models, Genetic Mutation, Missense/genetics Protein Conformation Protein Folding Proteins/genetics,metabolism Selection, Genetic
Chemicals
Proteins DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
DePristo Mark A
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138, USA. mark_depristo@harvard.edu
Weinreich Daniel M
Hartl Daniel L
Article Info
Journal
Nature reviews. Genetics
Abbr.
Nat Rev Genet
ISSN
1471-0056
Published
2005-09-00
Pages
678-87
Language
English
Region
England
NLM ID
100962779
Subset
IM
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