Allostery and cooperativity revisited

TitleAllostery and cooperativity revisited
Publication TypeJournal Article
Year of Publication2008
AuthorsCui, Q, Karplus, M
JournalProtein Science
Volume17
Pagination1295-1307
Date PublishedAug
Accession NumberISI:000258058200001
Keywordsallostery, Biochemistry & Molecular Biology, chaperones, chaperonin groel, conformational change, conformational-change, crystal-structure, hemoglobins, molecular, MWC, Pauling-KNF, protein allostery, protein dynamics, Scapharca dimeric hemoglobin, signal-transduction, structural transitions, tetrameric, threonine deaminase
Abstract

Although phenomenlogical models that account for cooperativity in allosteric systems date back to the early and mid- 60' s ( e. g., the KNF and MWC models), there is resurgent interest in the topic due to the recent experimental and computational studies that attempted to reveal, at an atomistic level, how allostery actually works. In this review, using systems for which atomistic simulations have been carried out in our groups as examples, we describe the current understanding of allostery, how the mechanisms go beyond the classical MWC/ Pauling- KNF descriptions, and point out that the `` new view'' of allostery, emphasizing `` population shifts,'' is, in fact, an `` old view.'' The presentation offers not only an up- to- date description of allostery from a theoretical/ computational perspective, but also helps to resolve several outstanding issues concerning allostery.

Short TitleProtein Sci