Schibeci A, Fincher G B, Stone B A, Wardrop A B
Biochem J. 1982 Sep 1;205(3):511-9. doi: 10.1042/bj2050511.
Plasma membranes have been isolated from protoplasts of suspension-cultured ryegrass (Lolium multiflorum) endosperm cells. The protoplast membrane is coated before cell disruption with murine myeloma protein J539, a galactose-binding immunoglobulin A. The plasma membrane is labelled with 125I by using chemically or enzymically catalysed iodination techniques, or, more conveniently, by using 125I-labelled myeloma protein J539, which enables the membrane to be simultaneously coated and labelled. Protoplast lysis is effected by gentle mechanical means after swelling in hypo-osmotic medium. The plasma-membrane fraction is recovered at low centrifugal forces by fractionation of cell lysates on a discontinuous sucrose/sorbitol gradient. The plasma-membrane fraction is enriched 96-fold on a protein basis with respect to the specific radioactivity of 125I-labeled myeloma protein J539 in the homogenate. Electron microscopy showed long membrane profiles often associated with one another.
已从悬浮培养的黑麦草(多花黑麦草)胚乳细胞的原生质体中分离出质膜。在用鼠骨髓瘤蛋白J539(一种半乳糖结合免疫球蛋白A)对细胞进行破坏之前,先对原生质体膜进行包被。通过化学或酶催化碘化技术,或者更方便地,使用125I标记的骨髓瘤蛋白J539对质膜进行125I标记,这使得膜能够同时被包被和标记。在低渗培养基中膨胀后,通过温和的机械方法使原生质体裂解。通过在不连续的蔗糖/山梨醇梯度上对细胞裂解物进行分级分离,在低离心力下回收质膜部分。相对于匀浆中125I标记的骨髓瘤蛋白J539的比放射性,质膜部分在蛋白质基础上富集了96倍。电子显微镜显示长的膜轮廓常常相互关联。