Literature DB >> 9949768

Design of protein function by physical perturbation method.

S Kidokoro1.   

Abstract

Based on three-dimensional structure of proteins, a rational strategy to design the protein function by physical perturbation method was proposed and tested on one of the well-examined enzymes, thermolysin for higher catalytic activity. An attempt was made to change the electrostatic potential and the dynamic property of three-dimensional structure around the active sites by single-amino-acid mutations, and the physical property of the mutants was then evaluated. Several mutants were found to have remarkably higher enzymatic activity than wild type. The multiple mutation was introduced and the logarithm of the activity was found to be almost additive. A ten times higher active mutant was realized by simultaneously introducing three single-mutations. This strategy can be easily extended to not only other enzymes but also other kinds of proteins than enzymes to modify or control the protein function based on their three-dimensional structures.

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Year:  1998        PMID: 9949768     DOI: 10.1016/s0065-227x(98)90007-7

Source DB:  PubMed          Journal:  Adv Biophys        ISSN: 0065-227X


  3 in total

1.  Contribution of proton linkage to the thermodynamic stability of the major cold-shock protein of Escherichia coli CspA.

Authors:  S A Petrosian; G I Makhatadze
Journal:  Protein Sci       Date:  2000-02       Impact factor: 6.725

2.  Effect of leucine-to-methionine substitutions on the diffraction quality of histone chaperone SET/TAF-Ibeta/INHAT crystals.

Authors:  Miki Senda; Shinsuke Muto; Masami Horikoshi; Toshiya Senda
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2008-09-30

3.  The impact of a single-nucleotide mutation of bgl2 on cellulase induction in a Trichoderma reesei mutant.

Authors:  Yosuke Shida; Kaori Yamaguchi; Mikiko Nitta; Ayana Nakamura; Machiko Takahashi; Shun-Ichi Kidokoro; Kazuki Mori; Kosuke Tashiro; Satoru Kuhara; Tomohiko Matsuzawa; Katsuro Yaoi; Yasumitsu Sakamoto; Nobutada Tanaka; Yasushi Morikawa; Wataru Ogasawara
Journal:  Biotechnol Biofuels       Date:  2015-12-30       Impact factor: 6.040

  3 in total

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