Matuo Y, Wheeler M A, Bitensky M W
Proc Natl Acad Sci U S A. 1976 Aug;73(8):2654-8. doi: 10.1073/pnas.73.8.2654.
Exposure of cholera toxin to membrane particles prepared from sarcoma 180 cells gives rise to a variety of fragments which are capable of activating adenylate cyclase [ATP:pyrophosphate-lyase (cyclizing), EC 4.6.1.1]. A major component of these fragments has an apparent molecular weight in the 8,000-10,000 range. The smallest stimulatory fragment has a molecular weight of approximately 1400. The small size of the fragments is confirmed by Sephadex gel filtration, in the presence of either sodium dodecyl sulfate or formic acid. These fragments are produced from holotoxin or its A subunit by protease(s) found in sarcoma membrane particles. Production of fragments appears optimal in 40-60 min at 30 degrees and pH 7, and is prevented by protease inhibitors. The ability of the small fragments to activate adenylate cyclase is reversed by anti-holotoxin, but not anticholeragenoid, antibodies. These fragments require NAD for the activation of adenylate cyclase and are fully active after heating at 90 degrees for 5 min (pH 7).
将霍乱毒素与由肉瘤180细胞制备的膜颗粒接触会产生多种片段,这些片段能够激活腺苷酸环化酶[ATP:焦磷酸裂解酶(环化),EC 4.6.1.1]。这些片段的主要成分表观分子量在8000 - 10000范围内。最小的刺激片段分子量约为1400。在十二烷基硫酸钠或甲酸存在的情况下,通过Sephadex凝胶过滤证实了片段的小尺寸。这些片段是由肉瘤膜颗粒中发现的蛋白酶从全毒素或其A亚基产生的。片段的产生在30℃和pH 7条件下40 - 60分钟时似乎最佳,并且被蛋白酶抑制剂阻止。小片段激活腺苷酸环化酶的能力可被抗全毒素抗体逆转,但不能被抗类霍乱原抗体逆转。这些片段激活腺苷酸环化酶需要NAD,并且在90℃加热5分钟(pH 7)后仍具有完全活性。