Literature DB >> 19666553

Conformational selection or induced fit: a flux description of reaction mechanism.

Gordon G Hammes1, Yu-Chu Chang, Terrence G Oas.   

Abstract

The mechanism of ligand binding coupled to conformational changes in macromolecules has recently attracted considerable interest. The 2 limiting cases are the "induced fit" mechanism (binding first) or "conformational selection" (conformational change first). Described here are the criteria by which the sequence of events can be determined quantitatively. The relative importance of the 2 pathways is determined not by comparing rate constants (a common misconception) but instead by comparing the flux through each pathway. The simple rules for calculating flux in multistep mechanisms are described and then applied to 2 examples from the literature, neither of which has previously been analyzed using the concept of flux. The first example is the mechanism of conformational change in the binding of NADPH to dihydrofolate reductase. The second example is the mechanism of flavodoxin folding coupled to binding of its cofactor, flavin mononucleotide. In both cases, the mechanism switches from being dominated by the conformational selection pathway at low ligand concentration to induced fit at high ligand concentration. Over a wide range of conditions, a significant fraction of the flux occurs through both pathways. Such a mixed mechanism likely will be discovered for many cases of coupled conformational change and ligand binding when kinetic data are analyzed by using a flux-based approach.

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Year:  2009        PMID: 19666553      PMCID: PMC2728963          DOI: 10.1073/pnas.0907195106

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  47 in total

1.  Backbone dynamics in dihydrofolate reductase complexes: role of loop flexibility in the catalytic mechanism.

Authors:  M J Osborne; J Schnell; S J Benkovic; H J Dyson; P E Wright
Journal:  Biochemistry       Date:  2001-08-21       Impact factor: 3.162

2.  Network of coupled promoting motions in enzyme catalysis.

Authors:  Pratul K Agarwal; Salomon R Billeter; P T Ravi Rajagopalan; Stephen J Benkovic; Sharon Hammes-Schiffer
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

Review 3.  Multiple conformational changes in enzyme catalysis.

Authors:  Gordon G Hammes
Journal:  Biochemistry       Date:  2002-07-02       Impact factor: 3.162

Review 4.  A perspective on enzyme catalysis.

Authors:  Stephen J Benkovic; Sharon Hammes-Schiffer
Journal:  Science       Date:  2003-08-29       Impact factor: 47.728

5.  Kinetic analysis of the mechanism of Escherichia coli dihydrofolate reductase.

Authors:  M H Penner; C Frieden
Journal:  J Biol Chem       Date:  1987-11-25       Impact factor: 5.157

6.  Single-molecule and transient kinetics investigation of the interaction of dihydrofolate reductase with NADPH and dihydrofolate.

Authors:  Zhiquan Zhang; P T Ravi Rajagopalan; Tzvia Selzer; Stephen J Benkovic; Gordon G Hammes
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-20       Impact factor: 11.205

Review 7.  Structure, dynamics, and catalytic function of dihydrofolate reductase.

Authors:  Jason R Schnell; H Jane Dyson; Peter E Wright
Journal:  Annu Rev Biophys Biomol Struct       Date:  2004

8.  Construction and evaluation of the kinetic scheme associated with dihydrofolate reductase from Escherichia coli.

Authors:  C A Fierke; K A Johnson; S J Benkovic
Journal:  Biochemistry       Date:  1987-06-30       Impact factor: 3.162

9.  Folding and association of an extremely stable dimeric protein from Sulfolobus islandicus.

Authors:  Markus Zeeb; Georg Lipps; Hauke Lilie; Jochen Balbach
Journal:  J Mol Biol       Date:  2004-02-06       Impact factor: 5.469

10.  Dynamic NMR spectral analysis and protein folding: identification of a highly populated folding intermediate of rat intestinal fatty acid-binding protein by 19F NMR.

Authors:  I J Ropson; C Frieden
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

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  206 in total

1.  Effect of channel mutations on the uptake and release of the retinal ligand in opsin.

Authors:  Ronny Piechnick; Eglof Ritter; Peter W Hildebrand; Oliver P Ernst; Patrick Scheerer; Klaus Peter Hofmann; Martin Heck
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-19       Impact factor: 11.205

2.  Tunable kinetic proofreading in a model with molecular frustration.

Authors:  Andre M Lindo; Bruno F Faria; Fernao V de Abreu
Journal:  Theory Biosci       Date:  2011-09-24       Impact factor: 1.919

3.  Equilibrium fluctuations of a single folded protein reveal a multitude of potential cryptic allosteric sites.

Authors:  Gregory R Bowman; Phillip L Geissler
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-02       Impact factor: 11.205

4.  Excited protein states of human tear lipocalin for low- and high-affinity ligand binding revealed by functional AB loop motion.

Authors:  Oktay K Gasymov; Adil R Abduragimov; Ben J Glasgow
Journal:  Biophys Chem       Date:  2010-04-09       Impact factor: 2.352

5.  From induced fit to conformational selection: a continuum of binding mechanism controlled by the timescale of conformational transitions.

Authors:  Huan-Xiang Zhou
Journal:  Biophys J       Date:  2010-03-17       Impact factor: 4.033

6.  Conformational selection or induced fit? A critical appraisal of the kinetic mechanism.

Authors:  Austin D Vogt; Enrico Di Cera
Journal:  Biochemistry       Date:  2012-07-16       Impact factor: 3.162

7.  Segmental motions, not a two-state concerted switch, underlie allostery in CheY.

Authors:  Leanna R McDonald; Joshua A Boyer; Andrew L Lee
Journal:  Structure       Date:  2012-06-21       Impact factor: 5.006

8.  Energetics and kinetics of substrate analog-coupled staphylococcal nuclease folding revealed by a statistical mechanical approach.

Authors:  Takuya Mizukami; Shunta Furuzawa; Satoru G Itoh; Saho Segawa; Teikichi Ikura; Kunio Ihara; Hisashi Okumura; Heinrich Roder; Kosuke Maki
Journal:  Proc Natl Acad Sci U S A       Date:  2020-07-31       Impact factor: 11.205

9.  Rates and equilibrium constants of the ligand-induced conformational transition of an HCN ion channel protein domain determined by DEER spectroscopy.

Authors:  Alberto Collauto; Hannah A DeBerg; Royi Kaufmann; William N Zagotta; Stefan Stoll; Daniella Goldfarb
Journal:  Phys Chem Chem Phys       Date:  2017-06-14       Impact factor: 3.676

10.  p15PAF is an intrinsically disordered protein with nonrandom structural preferences at sites of interaction with other proteins.

Authors:  Alfredo De Biasio; Alain Ibáñez de Opakua; Tiago N Cordeiro; Maider Villate; Nekane Merino; Nathalie Sibille; Moreno Lelli; Tammo Diercks; Pau Bernadó; Francisco J Blanco
Journal:  Biophys J       Date:  2014-02-18       Impact factor: 4.033

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