Gutensohn W, Huber M
Hoppe Seylers Z Physiol Chem. 1975 Apr;356(4):431-6. doi: 10.1515/bchm2.1975.356.1.431.
Hypoxanthine phosphoribosyltransferase (EC 2.4.2.8) from rat brain or human erytherocytes can be irreversibly inactivated by incubation with periodate-oxidized analogues of the enzyme products GMP or IMP. This inhibition is specific and directed against the product binding site of the enzyme. Inactivation is not produced by periodate-oxidized AMP or other aldehydes, for example periodate-oxidized glycerol. The inactivation is concomitant with the binding of the inhibitor to the enzyme protein. The bound inhibitor cannot be removed from the protein by dialysis, Sephadex chromatography or polyacrylamide-gel electrophoresis. Adenine phosphoribosyltransferase (EC 2.4.2.7), on the other hand, is not influenced by any of the inhibitors mentioned above.
来自大鼠脑或人红细胞的次黄嘌呤磷酸核糖基转移酶(EC 2.4.2.8),与酶产物GMP或IMP的高碘酸盐氧化类似物一起温育时会被不可逆地失活。这种抑制作用具有特异性,且针对酶的产物结合位点。高碘酸盐氧化的AMP或其他醛类,如高碘酸盐氧化的甘油,不会产生失活作用。失活与抑制剂和酶蛋白的结合相伴发生。结合的抑制剂不能通过透析、葡聚糖凝胶色谱法或聚丙烯酰胺凝胶电泳从蛋白质中去除。另一方面,腺嘌呤磷酸核糖基转移酶(EC 2.4.2.7)不受上述任何一种抑制剂的影响。