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依他尼酸与牛脑微管蛋白的相互作用。

Interaction of ethacrynic acid with bovine brain tubulin.

作者信息

Ludueña R F, Roach M C, Epstein D L

机构信息

Department of Biochemistry, University of Texas Health Science Center at San Antonio 78284-7760.

出版信息

Biochem Pharmacol. 1994 Apr 29;47(9):1677-81. doi: 10.1016/0006-2952(94)90547-9.

Abstract

Ethacrynic acid is a diuretic agent that reacts with sulfhydryl groups in proteins, and which shows promise of effectiveness in the treatment of glaucoma. Ethacrynic acid is a known inhibitor of microtubule assembly in vitro (Xu et al., Arch Biochem Biophys 296: 462-67, 1992). We have used N,N'-ethylenebis (iodoacetamide) (EBI) as a probe to examine the sulfhydryl groups of tubulin; EBI can form two intra-chain cross-links in beta-tubulin. One of these, beta*, connects Cys239 with Cys354; the other, beta s, joins Cys12 with either Cys201 or Cys211 (Little and Ludueña, EMBO J 4: 51-56, 1985; Biochim Biophys Acta 912: 28-33, 1987). Formation of beta * inhibits microtubule assembly in vitro, consistent with the hypothesis that Cys239 has an assembly-critical sulfhydryl (Bai et al., Biochemistry 28: 5606-5612, 1989). We have examined the interaction of ethacrynic acid with the sulfhydryl groups of bovine brain tubulin. We found that 130 microM ethacrynic acid gave half-maximal inhibition of assembly, but had no effect on the formation of the beta * cross-link by EBI. Ethacrynic acid, however, did inhibit substantially formation of the beta s cross-link at this concentration and half-maximally inhibited it at approximately 185 microM. Half-maximal inhibition of the alkylation of tubulin sulfhydryls by iodo [14C]acetamide was obtained at an ethacrynic acid concentration in the range of 190-325 microM. These results indicate that ethacrynic acid can inhibit microtubule assembly by reacting with sulfhydryl groups other than those of Cys239 and Cys354 and suggest that other sulfhydryl groups in tubulin could be assembly-critical. These results also raise the possibility that these other assembly-critical sulfhydryls may be those of Cys12, Cys201 or Cys211.

摘要

依他尼酸是一种利尿剂,可与蛋白质中的巯基发生反应,在青光眼治疗方面显示出有效前景。依他尼酸是一种已知的体外微管组装抑制剂(Xu等人,《生物化学与生物物理学报》296: 462 - 67, 1992)。我们使用N,N'-亚乙基双(碘乙酰胺)(EBI)作为探针来检测微管蛋白的巯基;EBI可在β-微管蛋白中形成两个链内交联。其中一个,β*,将半胱氨酸239与半胱氨酸354连接起来;另一个,βs,将半胱氨酸12与半胱氨酸201或半胱氨酸211连接起来(Little和Ludueña,《欧洲分子生物学组织杂志》4: 51 - 56, 1985;《生物化学与生物物理学报》912: 28 - 33, 1987)。β的形成在体外抑制微管组装,这与半胱氨酸239具有对组装至关重要的巯基这一假设相符(Bai等人,《生物化学》28: 5606 - 5612, 1989)。我们研究了依他尼酸与牛脑微管蛋白巯基的相互作用。我们发现130微摩尔的依他尼酸产生半数最大组装抑制,但对EBI形成β交联没有影响。然而,依他尼酸在此浓度下确实显著抑制βs交联的形成,并在约185微摩尔时产生半数最大抑制。在依他尼酸浓度为190 - 325微摩尔范围内,碘[14C]乙酰胺对微管蛋白巯基烷基化的半数最大抑制得以实现。这些结果表明依他尼酸可通过与半胱氨酸239和半胱氨酸354之外的巯基发生反应来抑制微管组装,并表明微管蛋白中的其他巯基可能对组装至关重要。这些结果还提出了一种可能性,即这些其他对组装至关重要的巯基可能是半胱氨酸12、半胱氨酸201或半胱氨酸211的巯基。

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