Buttle D J, Ritonja A, Dando P M, Abrahamson M, Shaw E N, Wikstrom P, Turk V, Barrett A J
Biochemistry Department, Strangeways Research Laboratory, Worts Causeway, Cambridge, England.
FEBS Lett. 1990 Mar 12;262(1):58-60. doi: 10.1016/0014-5793(90)80153-a.
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 alpha 2-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.
木瓜蛋白酶IV(PPIV)不像木瓜蛋白酶超家族的大多数其他蛋白酶那样,不受鸡半胱氨酸蛋白酶抑制剂或人半胱氨酸蛋白酶抑制剂A或C的抑制。该酶通过对先前显示参与半胱氨酸蛋白酶抑制剂抑制活性的甘氨酰键进行有限的蛋白水解作用,使鸡半胱氨酸蛋白酶抑制剂和人半胱氨酸蛋白酶抑制剂C失活,但对半胱氨酸蛋白酶抑制剂A无作用。先前报道的“木瓜蛋白酶”对半胱氨酸蛋白酶抑制剂的有限蛋白水解作用是由于市售结晶木瓜蛋白酶被PPIV污染所致。PPIV与人α2-巨球蛋白缓慢结合。该酶被E-64以及在P1中含有甘氨酸且在P2中含有疏水侧链的肽基重氮甲烷不可逆地失活。PPIV与碘乙酸的反应极其缓慢。尽管P1中存在庞大的侧链,但PPIV仍被肽醛抑制,这表明这些可逆抑制剂并非作为底物类似物结合。