Kondo T, Dale G L, Beutler E
Biochim Biophys Acta. 1980 Oct 16;602(1):127-30. doi: 10.1016/0005-2736(80)90295-3.
The preparation of inside-out vesicles from human erythrocytes requires their separation from contaminating right-side-out vesicles. We have taken advantage of the fact that there are no glycoproteins on the internal side of the erythrocyte membrane; therefore, inside-out vesicles do not interact with the lectin, concanavalin A, while right-side-out vesicles do interact. A concanavalin A-cellulose affinity matrix has been utilized to separate easily inside-out vesicles with a purity comparable to those prepared by prolonged centrifugation.
从人红细胞制备外翻小泡需要将其与污染的正常取向小泡分离。我们利用了红细胞膜内侧不存在糖蛋白这一事实;因此,外翻小泡不与伴刀豆球蛋白A凝集素相互作用,而正常取向小泡则会相互作用。已使用伴刀豆球蛋白A - 纤维素亲和基质轻松分离外翻小泡,其纯度与通过长时间离心制备的小泡相当。