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The interface of protein structure, protein biophysics, and molecular evolution

  • David A. Liberles
  • , Sarah A. Teichmann
  • , Ivet Bahar
  • , Ugo Bastolla
  • , Jesse Bloom
  • , Erich Bornberg-Bauer
  • , Lucy J. Colwell
  • , A. P.Jason De Koning
  • , Nikolay V. Dokholyan
  • , Julian Echave
  • , Arne Elofsson
  • , Dietlind L. Gerloff
  • , Richard A. Goldstein
  • , Johan A. Grahnen
  • , Mark T. Holder
  • , Clemens Lakner
  • , Nicholas Lartillot
  • , Simon C. Lovell
  • , Gavin Naylor
  • , Tina Perica
  • David D. Pollock, Tal Pupko, Lynne Regan, Andrew Roger, Nimrod Rubinstein, Eugene Shakhnovich, Kimmen Sjølander, Shamil Sunyaev, Ashley I. Teufel, Jeffrey L. Thorne, Joseph W. Thornton, Daniel M. Weinreich, Simon Whelan
  • University of Wyoming
  • Medical Research Council
  • Universidad Autónoma de Madrid
  • Fred Hutchinson Cancer Research Center
  • University of Münster
  • University of Colorado Anschutz Medical Campus
  • University of North Carolina at Chapel Hill
  • Universidad Nacional de San Martin
  • Stockholm University
  • University of California at Santa Cruz
  • University of Kansas
  • North Carolina State University
  • University of Montreal
  • University of Manchester
  • College of Charleston
  • Tel Aviv University
  • Yale University
  • Dalhousie University
  • Harvard University
  • University of California at Berkeley
  • Brigham and Women’s Hospital
  • University of Oregon
  • The University of Chicago
  • Brown University

Research output: Contribution to journalReview articlepeer-review

177 Scopus citations

Abstract

The interface of protein structural biology, protein biophysics, molecular evolution, and molecular population genetics forms the foundations for a mechanistic understanding of many aspects of protein biochemistry. Current efforts in interdisciplinary protein modeling are in their infancy and the state-of-the art of such models is described. Beyond the relationship between amino acid substitution and static protein structure, protein function, and corresponding organismal fitness, other considerations are also discussed. More complex mutational processes such as insertion and deletion and domain rearrangements and even circular permutations should be evaluated. The role of intrinsically disordered proteins is still controversial, but may be increasingly important to consider. Protein geometry and protein dynamics as a deviation from static considerations of protein structure are also important. Protein expression level is known to be a major determinant of evolutionary rate and several considerations including selection at the mRNA level and the role of interaction specificity are discussed. Lastly, the relationship between modeling and needed high-throughput experimental data as well as experimental examination of protein evolution using ancestral sequence resurrection and in vitro biochemistry are presented, towards an aim of ultimately generating better models for biological inference and prediction.

Original languageEnglish
Pages (from-to)769-785
Number of pages17
JournalProtein Science
Volume21
Issue number6
DOIs
StatePublished - Jun 2012

Keywords

  • Ancestral sequence reconstruction
  • Domain evolution
  • Evolutionary modeling
  • Gene duplication
  • Protein dynamics
  • Protein expression
  • Protein thermodynamics
  • Sequence-structure-function relationships

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