Repanovici R, Iliescu R, Lober G, Cajal N, Popa L M
Acta Virol. 1985 Dec;29(6):499-504.
Anthracycline antibiotics violamycin BI (VBI) and adriamycin (Adr) strongly inhibited the neuraminidase (NA) activity of Sendai virus and of its isolated glycoproteins, occurring either in solution or associated in liposome-like particles. NA did not exhibit the classical Michaelis-Menten kinetics: the plot of reaction velocity versus substrate concentration was sigmoidal, while Hill's plotting indicated that the enzyme has at least two binding sites for the substrate. The reaction kinetics obtained suggested that Sendai virus NA acts as an allosteric enzyme, when its material support, the HN is located on the virus surface. The inhibitory effect of the anthracycline antibiotics in question on the NA activity seemed to be similar to that of negative effectors.
蒽环类抗生素紫霉素BI(VBI)和阿霉素(Adr)强烈抑制仙台病毒及其分离的糖蛋白的神经氨酸酶(NA)活性,这些糖蛋白存在于溶液中或与脂质体样颗粒结合。NA不表现出经典的米氏动力学:反应速度与底物浓度的关系图呈S形,而希尔作图表明该酶至少有两个底物结合位点。所获得的反应动力学表明,当仙台病毒NA的物质支持物血凝素-神经氨酸酶(HN)位于病毒表面时,它作为一种别构酶起作用。上述蒽环类抗生素对NA活性的抑制作用似乎与负效应物的作用相似。