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Characterization of the Dielectric Constant in the Trichoderma reesei Cel7B Active Site
Author(s) -
Xiangfei Song,
Yefei Wang,
Shujun Zhang,
Shihai Yan,
Tong Li,
Lishan Yao
Publication year - 2015
Publication title -
journal of chemical information and modeling
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.24
H-Index - 160
eISSN - 1549-960X
pISSN - 1549-9596
DOI - 10.1021/acs.jcim.5b00155
Subject(s) - trichoderma reesei , dielectric , oniom , chemistry , active site , chemical physics , charge (physics) , substrate (aquarium) , catalysis , molecular dynamics , constant (computer programming) , computational chemistry , materials science , enzyme , organic chemistry , physics , optoelectronics , computer science , programming language , oceanography , quantum mechanics , geology , cellulase
An attempt is made to evaluate the dielectric constant of the Trichoderma reesei Cel7B active site. Through kinetic measurements, the pKa value of the catalytic acid E201 is determined. Mutations (away from E201) with net charge changes are introduced to perturb the E201 pKa. It is shown that the mutation with a +1 charge change (including G225R, G230R, and A335R) decreases the pKa of E201, whereas the mutation with a -1 charge change (including Q149E, A222D, G225D, and G230D) increases the pKa. This effect is consistent with the electrostatic interaction between the changed charge and the E201 side chain. The fitting of the experimental data yields an apparent dielectric constant of 25-80. Molecular dynamics simulations with explicit water molecules indicate that the high solvent accessibility of the active site contributes largely to the high dielectric constant. ONIOM calculations show that high dielectric constant benefits the catalysis through decreasing the energy of the transition state relative to that of the enzyme substrate complex.

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