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Title: Identification and modification of dynamical regions in proteins for alteration of enzyme catalytic effect

Patent ·
OSTI ID:1226810

A method for analysis, control, and manipulation for improvement of the chemical reaction rate of a protein-mediated reaction is provided. Enzymes, which typically comprise protein molecules, are very efficient catalysts that enhance chemical reaction rates by many orders of magnitude. Enzymes are widely used for a number of functions in chemical, biochemical, pharmaceutical, and other purposes. The method identifies key protein vibration modes that control the chemical reaction rate of the protein-mediated reaction, providing identification of the factors that enable the enzymes to achieve the high rate of reaction enhancement. By controlling these factors, the function of enzymes may be modulated, i.e., the activity can either be increased for faster enzyme reaction or it can be decreased when a slower enzyme is desired. This method provides an inexpensive and efficient solution by utilizing computer simulations, in combination with available experimental data, to build suitable models and investigate the enzyme activity.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-00OR22725
Assignee:
UT-Battelle, LLC (Oak Ridge, TN)
Patent Number(s):
9,195,795
Application Number:
13/086,603
OSTI ID:
1226810
Resource Relation:
Patent File Date: 2011 Apr 14
Country of Publication:
United States
Language:
English

References (15)

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Cis/trans isomerization in HIV-1 capsid protein catalyzed by cyclophilin A: Insights from computational and theoretical studies journal May 2004
Role of Protein Dynamics in Reaction Rate Enhancement by Enzymes journal November 2005
Network of coupled promoting motions in enzyme catalysis journal February 2002
Protein Dynamics and Enzymatic Catalysis:  Investigating the Peptidyl−Prolyl Cis−Trans Isomerization Activity of Cyclophilin A journal August 2004
Identification of slow correlated motions in proteins using residual dipolar and hydrogen-bond scalar couplings journal September 2005
Picosecond conformational transition and equilibration of a cyclic peptide journal May 2003
Dynamics of large proteins through hierarchical levels of coarse-grained structures journal November 2001
Enzyme Dynamics During Catalysis journal February 2002
Intrinsic dynamics of an enzyme underlies catalysis journal November 2005
Interfacing Electronic Structure Theory with Dynamics journal January 1996
Gaussian Dynamics of Folded Proteins journal October 1997
Vibrational Normal Modes of Polymer Nanoparticle Dimers Using the Time-Averaged Normal Coordinate Analysis Method journal October 2002
A dynamic reaction coordinate approach to a b i n i t i o reaction pathways: Application to the 1,5 hexadiene Cope rearrangement journal October 1990
Not just your average structures journal July 1996

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