Structural insights and functional implications of choline acetyltransferase

被引:24
作者
Govindasamy, L
Pedersen, B
Wei, L
Kukar, T
Gu, YR
Jin, SG
Agbandje-Mckenna, M
Wu, DH [1 ]
McKenna, R
机构
[1] McKnight Brain Inst, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
[2] Univ Florida, Gainesville, FL 32611 USA
[3] McKnight Brain Inst, Dept Med Chem, Gainesville, FL 32610 USA
[4] McKnight Brain Inst, Dept Microbiol & Mol Genet, Gainesville, FL 32610 USA
[5] Shanghai Inst Nutr Sci, Shanghai, Peoples R China
关键词
choline acetyltransferase; acetylcholine; neurotransmitter; X-ray structure; congenital myasthenic syndrome with episodic apnea;
D O I
10.1016/j.jsb.2004.06.005
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
The biosynthetic enzyme for the neurotransmitter acetylcholine, choline acetyltransferase (ChAT) (E.C. 2.3.1.6), is essential for the development and neuronal activities of cholinergic systems involved in many fundamental brain functions. ChAT catalyzes the transfer of an acetyl group from acetyl-coenzyme A to choline to form the neurotransmitter acetylcholine. Since its discovery more than 60 years ago much research has been devoted to the kinetic studies of this enzyme. For the first time we report the crystal structure of rat ChAT (rChAT) to 1.55 (A) over circle resolution. The structure of rChAT is a monomer and consists of two domains with an interfacial active site tunnel. This structure, with the modeled substrate binding, provides critical insights into the molecular basis for the production of acetylcholine and may further our understanding of disease causing mutations. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:226 / 235
页数:10
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