Interactions underlying subunit association in cholinesterases

被引:36
作者
Giles, K
机构
[1] WEIZMANN INST SCI, DEPT NEUROBIOL, IL-76100 REHOVOT, ISRAEL
[2] UNIV OXFORD, DEPT PHARMACOL, OXFORD OX1 3QT, ENGLAND
来源
PROTEIN ENGINEERING | 1997年 / 10卷 / 06期
关键词
cholinesterase; tetramer model; quaternary structure;
D O I
10.1093/protein/10.6.677
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
Cholinesterases occur in a family of molecular forms, both as homo-oligomers of catalytic subunits, which can be either soluble, amphiphilic or lipid-anchored to the membrane; and hetero-oligomers of catalytic submits and structural subunits, The structural subunits afford a method for precise localization of cholinesterases for specific function, A number of mutagenesis studies suggest that the C-terminal region of one alternatively spliced form of cholinesterase is involved in association of catalytic subunits into tetramers and in the association of these tetramers with structural subunits, however, there is currently no structural information about this region. In addition, none of the mutagenesis studies have clearly defined the residues important in these interactions. Here, multiple sequence alignment, structure prediction techniques and analysis of three-dimensional structural data are combined with a re-examination of mutagenesis and biochemical data. Three-dimensional models for the C-terminal region and for soluble tetrameric cholinesterase are proposed, and a set of rules governing subunit association are formulated, The simple model for association of catalytic and structural subunits presented is consistent with data for all known cholinesterases from species as divergent as nematode and man.
引用
收藏
页码:677 / 685
页数:9
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