CM‐cellulose chromatography of calf brain extracts revealed the presence of several enzymes hydrolysing benzoyiarginyl‐β‐naphthylamide (Bz‐Arg‐Nap) one of which resembled cathepsin B (EC 3.4.22.1). The latter was purified to homogeneity and showed an absolute dependence on thiol compounds and was optimally active at pH 6.5. The molecular weight of the purified enzyme was 27000 ± 1500. Purified enzyme was inhibited by leupeptin, antipain, iodoacetate, Hg2+, zn2+, and partially by chymostatin and phenylmethylsulfonyl fluoride but was unaffected by pepstatin, puromycin, bestatin and bacitracin. The Km with Bz‐Arg‐Nap was 0.53 mM, Kcat 4.5 min−1. Dipeptidyl and tripeptidyl‐acrylamide substrates were hydrolysed also by the brain enzyme but with lower Kcat/Km ratios. Comparison of the kinetics of inhibition using leupeptin (Ac‐l‐Leu‐Leu‐arginal) with Boc‐d‐Phe‐Pro‐arginal showed that the latter was non‐competitive and the former competitive with Ki of 1.5*10−8 M and 8*10−7 M respectively. Purified enzyme hydrolysed histones (lysine‐rich and type‐1), myelin basic protein, porcine β‐lipotropin, human β‐endorphin and protamine. Hydrolysis of β‐lipotropin was accompanied by the generation of a 8000‐Mr fragment. Cathepsin‐B‐like enzymes were present in highest concentration in rat pituitary, and lower in cerebellum, hypothalamus, medulla oblongata, striatum and spinal cord.
No takes yet. Share an insight, caveat, or question.
Suhar et al. (1979) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: