Kirschke H, Wikstrom P, Shaw E
Physiologisch-Chemisches Institut der Martin-Luther-Universität, Halle-Wittenberg, Saale, GDR.
FEBS Lett. 1988 Feb 8;228(1):128-30. doi: 10.1016/0014-5793(88)80600-8.
The substrate peptide bond cleaved by cathepsins B and L is determined not by the amino acid contributing the carboxyl group to this bond as in the case of serine proteases but rather by the presence of a neighboring amino acid with a large hydrophobic side chain. From a study of the inhibitory potency in a series, Cbz-Phe-X-CHN2, in which Phe promotes binding at S2 (terminology of [(1968) Biochem. Biophys. Res. Commun. 32, 898-902]) while the amino acid X probes S1, it is shown that this region of cathepsin L also has the ability to accommodate large hydrophobic side chains. In this respect cathepsin L differs from cathepsin B. Thus Cbz-Phe-Tyr(O-t-Bu)CHN2 inactivates cathepsin L with a rate 2.5 x 10(4) greater than that for cathepsin B.
组织蛋白酶B和L所切割的底物肽键,并非像丝氨酸蛋白酶那样由为该肽键提供羧基的氨基酸决定,而是由带有大的疏水侧链的相邻氨基酸的存在所决定。通过对一系列Cbz-Phe-X-CHN₂的抑制效力进行研究(其中Phe促进在S2位点的结合[术语源自(1968) Biochem. Biophys. Res. Commun. 32, 898 - 902],而氨基酸X探测S1位点),结果表明组织蛋白酶L的这一区域也能够容纳大的疏水侧链。在这方面,组织蛋白酶L与组织蛋白酶B不同。因此,Cbz-Phe-Tyr(O-t-Bu)CHN₂使组织蛋白酶L失活的速率比组织蛋白酶B高2.5×10⁴倍。