Goins B, Freire E
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.
Biochemistry. 1988 Mar 22;27(6):2046-52. doi: 10.1021/bi00406a035.
The thermal stability of cholera toxin free in solution and in association with its cell-surface receptor ganglioside GM1 has been studied by using high-sensitivity differential scanning calorimetry and differential solubility thermal gel analysis. In the absence of ganglioside GM1, cholera toxin undergoes two distinct thermally induced transitions centered at 51 and 74 degrees C, respectively. The low-temperature transition has been assigned to the irreversible thermal denaturation of the active A subunit. The second transition has been assigned to the reversible unfolding of the B subunit pentamer. The isolated B subunit pentamer exhibits a single transition also centered at 74 degrees C, suggesting that the attachment of the A subunit does not contribute to the stability of the pentamer. In the intact toxin, the A subunit dissociates from the B subunit pentamer at a temperature that coincides with the onset of the B subunit thermal unfolding. In aqueous solution, the denatured A subunit precipitates after dissociation from the B subunit pentamer. This phenomenon can be detected calorimetrically by the appearance of an exothermic heat effect. In the presence of ganglioside GM1, the B subunit is greatly stabilized as indicated by an increase of 20 degrees C in the transition temperature. In addition, ganglioside GM1 greatly enhances the cooperative interactions between B subunits. In the absence of ganglioside, each monomer within the B pentamer unfolds in an independent fashion whereas the fully ganglioside-bound pentamer behaves as a single cooperative unit. On the contrary, the thermotropic behavior of the A subunit is only slightly affected by the presence of increasing concentrations of ganglioside GM1.(ABSTRACT TRUNCATED AT 250 WORDS)
利用高灵敏度差示扫描量热法和差示溶解度热凝胶分析法,研究了溶液中游离的霍乱毒素及其与细胞表面受体神经节苷脂GM1结合时的热稳定性。在没有神经节苷脂GM1的情况下,霍乱毒素经历两个不同的热诱导转变,分别以51℃和74℃为中心。低温转变被认为是活性A亚基的不可逆热变性。第二个转变被认为是B亚基五聚体的可逆解折叠。分离的B亚基五聚体也表现出一个以74℃为中心的单一转变,这表明A亚基的附着对五聚体的稳定性没有贡献。在完整毒素中,A亚基在与B亚基热解折叠开始相吻合的温度下从B亚基五聚体上解离。在水溶液中,变性的A亚基从B亚基五聚体解离后沉淀。这种现象可以通过放热热效应的出现用热量法检测到。在存在神经节苷脂GM1的情况下,B亚基的稳定性大大提高,转变温度升高了20℃。此外,神经节苷脂GM1大大增强了B亚基之间的协同相互作用。在没有神经节苷脂的情况下,B五聚体内的每个单体以独立的方式解折叠,而完全与神经节苷脂结合的五聚体则表现为一个单一的协同单元。相反,A亚基的热致行为仅受到浓度不断增加的神经节苷脂GM1的轻微影响。(摘要截短于250字)