INTERACTION OF ETHACRYNIC-ACID WITH BOVINE BRAIN TUBULIN

Citation
Rf. Luduena et al., INTERACTION OF ETHACRYNIC-ACID WITH BOVINE BRAIN TUBULIN, Biochemical pharmacology, 47(9), 1994, pp. 1677-1681
Citations number
26
Categorie Soggetti
Pharmacology & Pharmacy",Biology
Journal title
ISSN journal
00062952
Volume
47
Issue
9
Year of publication
1994
Pages
1677 - 1681
Database
ISI
SICI code
0006-2952(1994)47:9<1677:IOEWBB>2.0.ZU;2-B
Abstract
Ethacrynic acid is a diuretic agent that reacts with sulfhydryl groups in proteins, and which shows promise of effectiveness in the treatmen t of glaucoma. Ethacrynic acid is a known inhibitor of microtubule ass embly in vitro (Xu et al., Arch Biochem Biophys 296: 462-67, 1992). We have used N,N'-ethylenebis (iodoacetamide) (EBI) as a probe to examin e the sulfhydryl groups of tubulin; EBI can form two intra-chain cross -links in beta-tubulin. One of these, beta, connects Cys(239) with Cy s(354); the other, beta(s), joins Cys(12) with either Cys(201) or Cys( 211) (Little and Luduena, 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 Cys(239) has an assembly-c ritical sulfhydryl (Bai et al., Biochemistry 28: 5606-5612, 1989). We have examined the interaction of ethacrynic acid with the sulfhydryl g roups of bovine brain tubulin. We found that 130 mu M ethacrynic acid gave half-maximal inhibition of assembly, but had no effect on the for mation of the beta cross-link by EBI. Ethacrynic acid, however, did i nhibit substantially formation of the beta(s) cross-link at this conce ntration and half-maximally inhibited it at approximately 185 mu M. Ha lf-maximal inhibition of the alkylation of tubulin sulfhydryls by iodo [C-14]acetamide was obtained at an ethacrynic acid concentration in t he range of 190-325 mu M. These results indicate that ethacrynic acid can inhibit microtubule assembly by reacting with sulfhydryl groups ot her than those of Cys(239) and Cys(354) and suggest that other sulfhyd ryl groups in tubulin could be assembly-critical. These results also r aise the possibility that these other assembly-critical sulfhydryls ma y be those of Cys(12), Cys(201) or Cys(211).