Mammalian chymotrypsin-like enzymes. Comparative reactivities of rat mast cell proteases, human and dog skin chymases, and human cathepsin G with peptide 4-nitroanilide substrates and with peptide chloromethyl ketone and sulfonyl fluoride inhibitors.
Mammalian chymotrypsin-like enzymes. Comparative reactivities of rat mast cell proteases, human and dog skin chymases, and human cathepsin G with peptide 4-nitroanilide substrates and with peptide chloromethyl ketone and sulfonyl fluoride inhibitors.
复制标题
哺乳动物胰凝乳蛋白酶样酶。
DOI:
10.1021/bi00329a037
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发表时间:
1985
期刊:
影响因子:
2.9
通讯作者:
Lazarus,GG
中科院分区:
文献类型:
--
作者:
Powers,JC;Tanaka,T;Harper,JW;Minematsu,Y;Barker,L;Lincoln,D;Crumley,KV;Fraki,JE;Schechter,NM;Lazarus,GG
Materials and Methods RMCP I and II were prepared as previously described (Everitt & Neurath, 1979; Woodbury & Neurath, 1978; Woodbury et al., 1981). Human and dog skin chymases were purified from the high-salt extract of skin by protamine pre-cipitation followed by gel filtration chromatography (Schechter et al., 1983). At this stage of purification, theydo not appear to be contaminated by other proteases. Human leukocyte cathepsin G was a gift fromDr. J. Travis and his research group at the University of Georgia. Bovine chymotrypsin Aa, TV-benzoyl-L-tyrosine ethyl ester, and chymostatin were pur-chased from Sigma Chemical Co., St. Louis, MO. The