The catalytic properties of human carbonic anhydrase IX

被引:78
作者
Wingo, T
Tu, C
Laipis, PJ
Silverman, DN
机构
[1] Univ Florida, Coll Med, Ctr Hlth, Dept Pharmacol & Therapeut, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
关键词
D O I
10.1006/bbrc.2001.5824
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
Human carbonic anhydrase IX (CA IX) is an integral membrane protein and a member of the a class of carbonic anhydrases that includes the human and animal enzymes. We have prepared a truncated, recombinant form of human CA IX of 255 residues consistent with full-length hv man CA II, among the most efficient of the carbonic anhydrases. Catalysis by and inhibition of this form of human CA IX has been investigated using stopped-flow spectrophotometry and O-18 exchange measured by mass spectrometry. In kinetic constants for the hydration of CO,, CA IX closely resembled CA II with maximal proton transfer-dependent O-18 exchange near I mus(-1) and k(cat)/K-m near 55 muM(-1) s(-1). Human CA IX was very strongly inhibited by three classic sulfonamides and cyanate, with inhibition constants that are close to those for CA Il. (C) 2001 Academic Press.
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收藏
页码:666 / 669
页数:4
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