Katz B A, Liu B, Barnes M, Springman E B
Arris Pharmaceutical Corporation, South San Francisco, California 94080, USA.
Protein Sci. 1998 Apr;7(4):875-85. doi: 10.1002/pro.5560070405.
Human tissue kallikrein, a trypsin-like serine protease involved in blood pressure regulation and inflammation processes, was expressed in a deglycosylated form at high levels in Pichia pastoris, purified, and crystallized. The crystal structure at 2.0 A resolution is described and compared with that of porcine kallikrein and of other trypsin-like proteases. The active and S1 sites (nomenclature of Schechter I, Berger A, 1967, Biochem Biophys Res Commun 27:157-162) are similar to those of porcine kallikrein. Compared to trypsin, the S1 site is enlarged owing to the insertion of an additional residue, cis-Pro 219. The replacement Tyr 228 --> Ala further enlarges the S1 pocket. However, the replacement of Gly 226 in trypsin with Ser in human tissue kallikrein restricts accessibility of substrates and inhibitors to Asp 189 at the base of the S1 pocket; there is a hydrogen bond between O delta1Asp189 and O gammaSer226. These changes in the architecture of the S1 site perturb the binding of inhibitors or substrates from the modes determined or inferred for trypsin. The crystal structure gives insight into the structural differences responsible for changes in specificity in human tissue kallikrein compared with other trypsin-like proteases, and into the structural basis for the unusual specificity of human tissue kallikrein in cleaving both an Arg-Ser and a Met-Lys peptide bond in its natural protein substrate, kininogen. A Zn+2-dependent, small-molecule competitive inhibitor of kallikrein (Ki = 3.3 microM) has been identified and the bound structure modeled to guide drug design.
人组织激肽释放酶是一种参与血压调节和炎症过程的胰蛋白酶样丝氨酸蛋白酶,它在毕赤酵母中以去糖基化形式高水平表达、纯化并结晶。描述了分辨率为2.0 Å的晶体结构,并与猪激肽释放酶和其他胰蛋白酶样蛋白酶的晶体结构进行了比较。活性位点和S1位点(Schechter I、Berger A,1967年命名法,《生物化学与生物物理研究通讯》27:157 - 162)与猪激肽释放酶的相似。与胰蛋白酶相比,由于额外插入了一个残基顺式脯氨酸219,S1位点扩大。酪氨酸228被丙氨酸取代进一步扩大了S1口袋。然而,人组织激肽释放酶中胰蛋白酶的甘氨酸226被丝氨酸取代,限制了底物和抑制剂接近S1口袋底部的天冬氨酸189;天冬氨酸189的Oδ1与丝氨酸226的Oγ之间存在氢键。S1位点结构的这些变化扰乱了抑制剂或底物与根据胰蛋白酶确定或推断的模式的结合。晶体结构揭示了与其他胰蛋白酶样蛋白酶相比人组织激肽释放酶特异性变化的结构差异,以及人组织激肽释放酶在其天然蛋白质底物激肽原中切割精氨酸 - 丝氨酸和甲硫氨酸 - 赖氨酸肽键的异常特异性的结构基础。已鉴定出一种锌离子依赖性的激肽释放酶小分子竞争性抑制剂(Ki = 3.3 μM),并对结合结构进行了建模以指导药物设计。