Epistasis and intramolecular networks in protein evolution.

Charlotte M Miton, Karol Buda, Nobuhiko Tokuriki

Journal: Current opinion in structural biology 2021;69():160-168

PMID: 34077895

Abstract

Proteins are molecular machines composed of complex, highly connected amino acid networks. Their functional optimization requires the reorganization of these intramolecular networks by evolution. In this review, we discuss the mechanisms by which epistasis, that is, the dependence of the effect of a mutation on the genetic background, rewires intramolecular interactions to alter protein function. Deciphering the biophysical basis of epistasis is crucial to our understanding of evolutionary dynamics and the elucidation of sequence-structure-function relationships. We featured recent studies that provide insights into the molecular mechanisms giving rise to epistasis, particularly at the structural level. These studies illustrate the convoluted and fascinating nature of the intramolecular networks co-opted by epistasis during the evolution of protein function.

Copyright © 2021 Elsevier Ltd. All rights reserved.

Address: Michael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, BC, Canada.; Michael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, BC, Canada. Electronic address: [email protected].

Link outs

Subscription / membership required

Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.