A novel microtubule independent effect of paclitaxel: the inhibition of peptidylarginine deiminase from bovine brain

被引:47
作者
Pritzker, LB [1 ]
Moscarello, MA [1 ]
机构
[1] Hosp Sick Children, Div Struct Biol & Biochem, Toronto, ON M5G 1X8, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY | 1998年 / 1388卷 / 01期
基金
英国医学研究理事会;
关键词
deimination; peptidylarginine deiminase; myelin basic protein; multiple sclerosis;
D O I
10.1016/S0167-4838(98)00175-7
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
Although the principal effect of paclitaxel (taxol) is in preventing depolymerization of microtubules, other effects have been described recently. In the present manuscript, we demonstrate an inhibitory effect on the enzyme peptidylarginine deiminase (PAD) which converts peptidyl bound arginine to citrulline. To study the mechanism of action of the drug on PAD, a number of studies were carried out with purified enzyme. With the synthetic substrate benzoyl-arginine ethyl ester (BAEE), almost total inhibition of activity was observed at 12.5 mM. With myelin basic protein (MBP) as a substrate, deimination of arginyl residues was prevented by 0.5 mM paclitaxel. The velocity-substrate curve was unusual since substrate enhancement was observed at 5 mM BAEE. These data suggested the presence of two binding sites on the enzyme. Inhibition of activity by paclitaxel was non-competitive for both sites. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:154 / 160
页数:7
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