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The role of dynamic conformational ensembles in biomolecular recognition

  1. Author:
    Boehr, D. D.
    Nussinov, R.
    Wright, P. E.
  2. Author Address

    Wright, Peter E.] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA. [Wright, Peter E.] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA. [Boehr, David D.] Penn State Univ, Dept Chem, University Pk, PA 16802 USA. [Nussinov, Ruth] NCI, Basic Sci Program, SAIC Frederick Inc, Ctr Canc Res Nanobiol Program, Frederick, MD 21701 USA. [Nussinov, Ruth] Tel Aviv Univ, Sackler Inst Mol Med, Dept Human Genet, Sackler Sch Med, IL-69978 Tel Aviv, Israel.
    1. Year: 2009
  1. Journal: Nature Chemical Biology
    1. 5
    2. 11
    3. Pages: 789-796
  2. Type of Article: Article
  1. Abstract:

    Molecular recognition is central to all biological processes. For the past 50 years, Koshland's 'induced fit' hypothesis has been the textbook explanation for molecular recognition events. However, recent experimental evidence supports an alternative mechanism. 'Conformational selection' postulates that all protein conformations pre-exist, and the ligand selects the most favored conformation. Following binding the ensemble undergoes a population shift, redistributing the conformational states. Both conformational selection and induced fit appear to play roles. Following binding by a primary conformational selection event, optimization of side chain and backbone interactions is likely to proceed by an induced fit mechanism. Conformational selection has been observed for protein-ligand, protein-protein, protein-DNA, protein-RNA and RNA-ligand interactions. These data support a new molecular recognition paradigm for processes as diverse as signaling, catalysis, gene regulation and protein aggregation in disease, which has the potential to significantly impact our views and strategies in drug design, biomolecular engineering and molecular evolution.

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External Sources

  1. DOI: 10.1038/nchembio.232
  2. PMID: 19841628

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