Moskaug J O, Sandvig K, Olsnes S
Institute for Cancer Research, Norwegian Radium Hospital, Montebello, Oslo.
J Biol Chem. 1989 Jul 5;264(19):11367-72.
Previous work has shown that when Vero cells with surface-bound diphtheria toxin are exposed to low pH, toxin entry across the plasma membrane is induced and that this entry involves two steps, insertion of the B-fragment of the toxin into the membrane and translocation of the enzymatically active A-fragment to the cytosol. Here we have studied the role of permeant anions in this process. It was found that when the B-fragment was inserted into the membrane, part of it, a 25-kDa polypeptide, was shielded from externally added Pronase. This insertion did not require permeant anions. The translocation of the A-fragment was monitored by measuring either its ability to inhibit protein synthesis in the cells or the appearance of radioactively labeled 21-kDa fragment after treatment of the cells with externally applied Pronase. The translocation of the A-fragment was dependent on the presence of permeant anions in the medium. However, when the cells were depleted of Cl- by incubation in Cl- free buffer at high pH, translocation of the A-fragment did not require permeant anions in the medium. The possibility that translocation of the A-fragment is inhibited by an outward directed chloride gradient rather than by the absence of chloride is discussed.
先前的研究表明,当表面结合有白喉毒素的Vero细胞暴露于低pH值环境时,毒素会诱导进入质膜,且这种进入涉及两个步骤,即毒素的B片段插入膜中以及具有酶活性的A片段转运至胞质溶胶。在此,我们研究了渗透性阴离子在此过程中的作用。结果发现,当B片段插入膜中时,其一部分,即一条25 kDa的多肽,对外源添加的链霉蛋白酶具有抗性。这种插入不需要渗透性阴离子。通过测量A片段抑制细胞内蛋白质合成的能力或在用外源链霉蛋白酶处理细胞后放射性标记的21 kDa片段的出现情况来监测A片段的转运。A片段的转运依赖于培养基中渗透性阴离子的存在。然而,当细胞在高pH值的无氯缓冲液中孵育而耗尽Cl-时,A片段的转运在培养基中不需要渗透性阴离子。本文讨论了A片段的转运被外向性氯离子梯度抑制而非被氯离子缺失抑制的可能性。