The effects of vanadate on human erythrocyte membrane have been investigated with stopped-flow and equilibrium fluorescence quenching techniques. The equilibrium study showed a half-quenching concentration(K 1/2 ) of ...The effects of vanadate on human erythrocyte membrane have been investigated with stopped-flow and equilibrium fluorescence quenching techniques. The equilibrium study showed a half-quenching concentration(K 1/2 ) of 0.27 mmol.L-1. The stopped-flow experiment exhibited a fast rise (tsk1/f1 S) and a slow drop (tin 1~2 min) in fluorescence. Based on the results and that from the across membrane transport of vanadate, a kinetic model is proposed which suggests that the membrane proteins experience a series of conformational changes before and during the quenching of the intrinsic fluorescence. These changes are induced mainly by three kinds of interactions: (i) the long-distance, non-specific interaction between the vanadate and the erythrocyte membrane surface, (ii) the charge interaction between the vanadate and parts of the membrane proteins, and(iii) the binding of the vanadate to some membrane proteins.展开更多
为探讨丙溴磷对人红细胞膜的毒性作用 ,检测了红细胞膜Ⅰ型补体受体 (Em -CR1)免疫粘附肿瘤细胞活性与红细胞超氧化物歧化酶 (E -SOD)活性、红细胞膜唾液酸 (Em -SA)含量以及红细胞膜脂流动性。结果发现 ,一定浓度丙溴磷可使上述各项指...为探讨丙溴磷对人红细胞膜的毒性作用 ,检测了红细胞膜Ⅰ型补体受体 (Em -CR1)免疫粘附肿瘤细胞活性与红细胞超氧化物歧化酶 (E -SOD)活性、红细胞膜唾液酸 (Em -SA)含量以及红细胞膜脂流动性。结果发现 ,一定浓度丙溴磷可使上述各项指标显著降低 ,并呈现剂量 -效应关系 。展开更多
基金Project supported by the National Natural Science Foundation of China (Grant No. 29471007).
文摘The effects of vanadate on human erythrocyte membrane have been investigated with stopped-flow and equilibrium fluorescence quenching techniques. The equilibrium study showed a half-quenching concentration(K 1/2 ) of 0.27 mmol.L-1. The stopped-flow experiment exhibited a fast rise (tsk1/f1 S) and a slow drop (tin 1~2 min) in fluorescence. Based on the results and that from the across membrane transport of vanadate, a kinetic model is proposed which suggests that the membrane proteins experience a series of conformational changes before and during the quenching of the intrinsic fluorescence. These changes are induced mainly by three kinds of interactions: (i) the long-distance, non-specific interaction between the vanadate and the erythrocyte membrane surface, (ii) the charge interaction between the vanadate and parts of the membrane proteins, and(iii) the binding of the vanadate to some membrane proteins.