INTERACTIONS OF PAPAYA PROTEINASE-IV WITH INHIBITORS

被引:39
作者
BUTTLE, DJ
RITONJA, A
DANDO, PM
ABRAHAMSON, M
SHAW, EN
WIKSTROM, P
TURK, V
BARRETT, AJ
机构
[1] J STEFAN INST, DEPT BIOCHEM, YU-61000 LJUBLJANA, YUGOSLAVIA
[2] UNIV LUND HOSP, DEPT CLIN CHEM, S-22185 LUND, SWEDEN
[3] FRIEDRICH MIESCHER INST, CH-4002 BASEL, SWITZERLAND
关键词
Compound E-64; Cystatin; Iodoacetamide; Iodoacetate; Macroglobulin; α[!sub]2[!/sub]-; Papain; Peptide aldehyde; Peptidyl diazomethane;
D O I
10.1016/0014-5793(90)80153-A
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
Papaya proteinase IV (PPIV) is not inhibited by chicken cystatin, or human cystatins A or C, unlike most other proteinases of the papain superfamily. The enzyme inactivates chicken cystatin and human cystatin C by limited proteolysis of the glycyl bond previously shown to be involved in the inhibitory inactivity of the cystatins, but has no action on cystatin A. Contamination of commercial crystalline papain with PPIV accounts for the limited proteolysis of cystatins by 'papain' reported previously. PPIV is slowly bound by human α2-macroglobulin. The enzyme is irreversibly inactivated by E-64, and by peptidyl diazomethanes containing glycine in P1 and a hydrophobic side-chain in P2. The reaction of PPIV with iodoacetate is extremely slow. PPIV is inhibited by peptide aldehydes despite the presence of bulky sidechains in P1, suggesting that these reversible inhibitors do not bind as substrate analogues. © 1990.
引用
收藏
页码:58 / 60
页数:3
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