Rolf J M, Gaudin H M, Eidels L
Department of Microbiology, University of Texas Southwestern Medical Center, Dallas 75235-9048.
J Biol Chem. 1990 May 5;265(13):7331-7.
The carboxyl-terminal Mr = 5982 peptide of diphtheria toxin was prepared by specific cleavage of the toxin with hydroxylamine and purified by fast performance liquid chromatography. The identity of the peptide was established by a combination of sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis, reactivity with specific monoclonal antibodies, and amino-terminal sequence analysis. The Mr = 5982 peptide was shown to protect highly toxin-sensitive Vero cells from the lethal action of diphtheria toxin. This protection was shown to be due to inhibition of the initial step in the cytotoxic process, the binding of toxin to its receptor. These results strongly suggest that the Mr = 5982 carboxyl-terminal region (amino acid residues 482-535) is, or contains, the receptor-binding domain of diphtheria toxin.
通过用羟胺对毒素进行特异性切割制备了白喉毒素的羧基末端Mr = 5982肽,并通过快速液相色谱法进行纯化。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析、与特异性单克隆抗体的反应性以及氨基末端序列分析相结合来确定该肽的身份。已证明Mr = 5982肽可保护高度毒素敏感的Vero细胞免受白喉毒素的致死作用。这种保护作用被证明是由于抑制了细胞毒性过程的起始步骤,即毒素与其受体的结合。这些结果强烈表明,Mr = 5982羧基末端区域(氨基酸残基482 - 535)是白喉毒素的受体结合结构域,或者包含该结构域。