Hsia J A, Tsai S C, Adamik R, Yost D A, Hewlett E L, Moss J
J Biol Chem. 1985 Dec 25;260(30):16187-91.
Hydroxylamine stability has been used to classify (ADP-ribose)protein bonds into sensitive and resistant linkages, with the former representing (ADP-ribose)glutamate, and the latter, (ADP-ribose)arginine. Recently, it was shown that cysteine also serves as an ADP-ribose acceptor. The hydroxylamine stability of [cysteine([32P]ADP-ribose)]protein and [arginine([32P] ADP-ribose)]protein bonds was compared. In transducin, pertussis toxin catalyzes the ADP-ribosylation of a cysteine residue, whereas choleragen (cholera toxin) modifies an arginine moiety. The (ADP-ribose)cysteine bond formed by pertussis toxin was more stable to hydroxylamine than was the (ADP-ribose)arginine bond formed by choleragen. The (ADP-ribose)cysteine bond apparently represents a third class of ADP-ribose bonds. Pertussis toxin ADP-ribosylates the inhibitory guanyl nucleotide-binding regulatory protein (Gi) of adenylate cyclase, whereas choleragen modifies the stimulatory guanyl nucleotide-binding regulatory protein (Gs). These (ADP-ribose)protein linkages are identical in stability to those formed in transducin by the two toxins, consistent with the probability that cysteine and arginine are modified in Gi and Gs, respectively. Bonds exhibiting differences in hydroxylamine-stability were found in membranes from various non-intoxicated mammalian cells following incubation with [32P]NAD, which may reflect the presence of endogenous NAD:protein-ADP-ribosyl-transferases.
羟胺稳定性已被用于将(ADP-核糖)蛋白质键分为敏感型和抗性型连接,前者代表(ADP-核糖)谷氨酸,后者代表(ADP-核糖)精氨酸。最近研究表明,半胱氨酸也可作为ADP-核糖的受体。比较了[半胱氨酸([³²P]ADP-核糖)]蛋白质和[精氨酸([³²P]ADP-核糖)]蛋白质键的羟胺稳定性。在转导素中,百日咳毒素催化半胱氨酸残基的ADP-核糖基化,而霍乱毒素修饰精氨酸部分。百日咳毒素形成的(ADP-核糖)半胱氨酸键比霍乱毒素形成的(ADP-核糖)精氨酸键对羟胺更稳定。(ADP-核糖)半胱氨酸键显然代表了第三类ADP-核糖键。百日咳毒素使腺苷酸环化酶的抑制性鸟苷酸结合调节蛋白(Gi)发生ADP-核糖基化,而霍乱毒素修饰刺激性鸟苷酸结合调节蛋白(Gs)。这些(ADP-核糖)蛋白质连接在稳定性上与两种毒素在转导素中形成的连接相同,这与半胱氨酸和精氨酸分别在Gi和Gs中被修饰的可能性一致。在用[³²P]NAD孵育后,在各种未中毒的哺乳动物细胞的膜中发现了羟胺稳定性存在差异的键,这可能反映了内源性NAD:蛋白质-ADP-核糖基转移酶的存在。