Larionova N I, Maslov E V, Eliseeva Iu E, Pavlikhina L V
Biokhimiia. 1982 Aug;47(8):1332-7.
The essentials of estimation of the number of enzyme active sites by reversible inhibition are discussed. The necessity of evaluation of the substrate effect on the equilibrium of the systems with a rapidly dissociating enzyme -- inhibitor complex has been demonstrated. Some procedures for determination of the number of active sites of dipeptidyl-carboxypeptidase (EC 3.4.15.1) from bovine kidney cortex, using the competitive inhibitor SQ 20 881 (Glu-Trp-Pro-Arg-Pro-Gln-Ile-Pro-Pro) have been developed. The kinetic and equilibrium constants for the enzyme-inhibitor interaction (ki = 3.2 . 10(6) M-1s-1, k-i = 8 ms-1 and Ki = 2.5 +/- 0.5 nm) have been calculated.
本文讨论了通过可逆抑制来估算酶活性位点数量的要点。已证明评估底物对具有快速解离的酶 - 抑制剂复合物的系统平衡的影响的必要性。已开发出一些使用竞争性抑制剂SQ 20 881(Glu-Trp-Pro-Arg-Pro-Gln-Ile-Pro-Pro)测定牛肾皮质中二肽基羧肽酶(EC 3.4.15.1)活性位点数量的方法。已计算出酶 - 抑制剂相互作用的动力学和平衡常数(ki = 3.2×10⁶ M⁻¹s⁻¹,k-i = 8 ms⁻¹和Ki = 2.5±0.5 nM)。