Chang T, Neville D M
J Biol Chem. 1978 Oct 10;253(19):6866-71.
A detailed binding study of 125I-labeled diphtheria toxin to isolated cell surface membrane-enriched fractions is reported. The study was undertaken to determine if toxin-resistant species exhibit a defet in either the binding step or the transport step of the intoxication process. Surface membrane fractions were obtained from liver and mammary glands of toxin-sensitive species, rabbit and giunea pig, and toxin-resistant species, rat mouse. All membrane fractions exhibited reversible binding of 125I-toxin which was competitively inhibited by unlabeled toxin. Toxin receptors from liver co-purified with plasma membranes and the plasma membrane marker 5'-nucleotidase. One-half saturation of all receptors occurred between 5 x 10(-8) and 1.8 x 10(-7) M. Scatchard plots were nonlinear and concave upwards. Total receptor sites ranged from 3.4 to 16 pmol/mg of membrane protein, tissue differences being more pronounced than difference between sensitive and nonsensitive species. Over 95% of the toxin specific binding was inhibited by removal of divalent cation from the medium or by the inclusion of 1 mM ATP, procedures which have been shown to protect sensitive cells from intoxication by diphtheria toxin. We conclude that the rat and mouse have surface membrane receptors for diphtheria toxin and that the toxin insensitivity of these species results from a defect in or a lack of the transport process.
本文报道了对125I标记的白喉毒素与分离的富含细胞表面膜的组分进行的详细结合研究。进行该研究是为了确定抗毒素物种在中毒过程的结合步骤或转运步骤中是否存在缺陷。从毒素敏感物种(兔和豚鼠)以及抗毒素物种(大鼠和小鼠)的肝脏和乳腺中获得表面膜组分。所有膜组分均表现出125I毒素的可逆结合,未标记的毒素可竞争性抑制这种结合。肝脏中的毒素受体与质膜和质膜标记物5'-核苷酸酶共纯化。所有受体的半饱和状态出现在5×10(-8)至1.8×10(-7)M之间。Scatchard图呈非线性且向上凹。总受体位点范围为3.4至16 pmol/mg膜蛋白,组织差异比敏感和不敏感物种之间的差异更明显。通过从培养基中去除二价阳离子或加入1 mM ATP可抑制超过95%的毒素特异性结合,这些方法已被证明可保护敏感细胞免受白喉毒素中毒。我们得出结论,大鼠和小鼠具有白喉毒素的表面膜受体,并且这些物种对毒素不敏感是由于转运过程中的缺陷或缺乏所致。