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Please use this identifier to cite or link to this item: http://eprint.iitd.ac.in/handle/2074/183

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dc.contributor.authorJayaram, B-
dc.contributor.authorDas, A-
dc.contributor.authorAneja, N-
dc.identifier.citationJournal of Molecular Structure (Theochem) 361,249-258en
dc.description.abstractA detailed molecular view of structural, thermodynamic and kinetic aspects is essential for a clear understanding of macromolecular association. We have recently assembled a force field to capture the energetics of protein-DNA inter- actions in aqueous solution, and to provide a thermodynamic and kinetic description of association in a computationally expeditious manner. An application of this force field to a X repressor-operator with a partitioning of the interaction energies on a subunit basis has revealed some interesting features. Hydrogen bonding and van der Waals interactions of the turn-recognition helix-turn subunit of the protein with the nucleic acid bases in the major groove appear to determine specificity in binding. Brownian dynamics simulations were performed on several models for the X repressor-operator system to monitor some mechanistic aspects, of relevance to kinetics of B mplexation. The calculated joint probability for a nonspecific association of protein and DNA, driven mostly by electrostatics, followed by a sliding of the protein to the active site (operator region) on the DNA, a search in reduced dimensional configuration space accessible to the system, is much more than the probability of a three-dimensional diffusion of the protein to the active site. Implications of these results to protein-DNA recognition are analyzed and discussed.en
dc.format.extent968,445 bytes-
dc.publisherElsevier Scienceen
dc.subjectthermodynamic and kineticen
dc.subjectX repressor-operatoren
dc.subjectnucleic aciden
dc.titleEnergetic and kinetic aspects of macromolecular association: computational study of X repressor-operator complexationen
Appears in Collections:Applied Mechanics

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