Koffer A, Edgar A
Department of Biophysics, King's College, London, U.K.
Biochim Biophys Acta. 1989 Jul 10;982(2):295-9. doi: 10.1016/0005-2736(89)90067-9.
Plasma membranes, isolated from normal (C13) and polyoma virus-transformed (J1) cultured BHK cells were incubated with G-actin under polymerizing conditions, followed by a low-speed centrifugation. The amount of actin attached to the pelleted BHK-J1 plasma membranes was at least twice that on BHK-C13 membranes, indicating a greater number of actin attachment sites on the former. This result was confirmed by the observation that the plasma membranes from the transformed cells were also more active in nucleating polymerization of pyrene-labelled actin. Most of the actin attachment sites could be solubilized by Triton or low-salt extraction treatment.
从正常(C13)和多瘤病毒转化(J1)的培养BHK细胞中分离出的质膜,在聚合条件下与G-肌动蛋白一起孵育,然后进行低速离心。附着在沉淀的BHK-J1质膜上的肌动蛋白量至少是BHK-C13膜上的两倍,表明前者上有更多的肌动蛋白附着位点。通过观察转化细胞的质膜在芘标记的肌动蛋白成核聚合中也更活跃,这一结果得到了证实。大多数肌动蛋白附着位点可以通过Triton或低盐提取处理溶解。