Effector proteins from P450cam and methane monooxygenase:: lessons in tuning nature's powerful reagents

被引:27
作者
Brazeau, BJ
Wallar, BJ
Lipscomb, JD [1 ]
机构
[1] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Ctr Met & Biocatalysis, Minneapolis, MN 55455 USA
关键词
methane monooxygenase; P450(cam); effector; kinetics; fluorescence; cross-linking; regulation; component docking;
D O I
10.1016/j.bbrc.2003.09.242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Effector proteins alter the kinetic or catalytic course of many oxygenase reactions. One of the first oxygenase effectors to be described was putidaredoxin. which serves to gate electron transfer into oxy-P450(cam). In the nonheme, methane monooxygenase (MMO) system, the B-component (MMOB) serves a distinct effector function by gating substrate and oxygen into the active site of the hydroxylase component (MMOH). Here the binding parameters and binding surfaces of the MMOB-MMOH complex are determined by site-specific labeling, fluorescence titrations, chemical cross-linking, and MALDI-TOF peptide identification. Based on these data, a model for the bimolecular complex is described and a hypothesis for the structural basis for the effector function is elaborated. The bearing on the putidaredoxin effector function is discussed. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:143 / 148
页数:6
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