首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Linkage of a membrane skeleton to integral membrane glycoproteins in human platelets. Identification of one of the glycoproteins as glycoprotein Ib.
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Linkage of a membrane skeleton to integral membrane glycoproteins in human platelets. Identification of one of the glycoproteins as glycoprotein Ib.

机译:膜骨架与人血小板中完整的膜糖蛋白的联系。将一种糖蛋白鉴定为糖蛋白Ib。

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摘要

Experiments were performed to determine whether platelets contain a membrane skeleton. Platelets were labeled by a sodium periodate/sodium [3H]borohydride method and lysed with Triton X-100. Much of the filamentous actin could be sedimented at low g forces (15,600 g, 4 min), but some of the actin filaments required high-speed centrifugation for their sedimentation (100,000 g, 3 h). The latter filaments differed from those in the low-speed pellet in that they could not be depolymerized by Ca2+ and could not be sedimented at low g forces even from Triton X-100 lysates of platelets that had been activated with thrombin. Actin-binding protein sedimented with both types of filaments, but 3H-labeled membrane glycoproteins were recovered mainly with the high-speed filaments. The primary 3H-labeled glycoprotein recovered with this "membrane skeleton" was glycoprotein (GP) Ib. Approximately 70% of the platelet GP Ib was present in this skeleton. Several other minor glycoproteins, including greater than 50% of the GP Ia and small amounts of three unidentified glycoproteins of Mr greater than 200,000, were also recovered with the membrane skeleton. The Triton X-100 insolubility of GP Ib, GP Ia, a minor membrane glycoprotein of 250,000 Mr, and actin-binding protein resulted from their association with actin filaments as they were rendered Triton X-100-soluble when actin filaments were depolymerized with deoxyribonuclease I and co-isolated with actin filaments on sucrose gradients. When isolated platelet plasma membranes were extracted with Triton X-100, actin, actin-binding protein, and GP Ib were recovered as the Triton X-100 residue. These studies show that unstimulated platelets contain a membrane skeleton composed of actin filaments and actin-binding protein that is distinct from the rest of the cytoskeleton and is attached to GP Ib, GP Ia, and a minor glycoprotein of 250,000 Mr on the plasma membrane.
机译:进行实验以确定血小板是否含有膜骨架。用高碘酸钠/ [3H]硼氢化钠方法标记血小板,并用Triton X-100裂解。许多丝状肌动蛋白可以在低g力(15,600 g,4分钟)下沉淀,但是一些肌动蛋白丝需要高速离心才能沉淀(100,000 g,3 h)。后者的细丝与低速沉淀物中的细丝的不同之处在于,即使由凝血酶活化的血小板的Triton X-100裂解物,它们也不会被Ca2 +解聚,也无法在低g力下沉降。肌动蛋白结合蛋白沉积在两种类型的细丝中,但3H标记的膜糖蛋白主要通过高速细丝回收。用此“膜骨架”回收的主要3H标记糖蛋白是糖蛋白(GP)Ib。该骨架中约有70%的血小板GP Ib存在。膜的骨架还回收了其他几种次要的糖蛋白,包括大于50%的GP Ia和少量的三种未鉴定的Mr大于200,000的糖蛋白。 GP Ib,GP Ia,250,000 Mr的次要膜糖蛋白和肌动蛋白结合蛋白的Triton X-100不溶性是由于它们与肌动蛋白丝的结合而产生的,因为当肌动蛋白丝通过脱氧核糖核酸酶解聚时,它们变成Triton X-100可溶的。我和肌动蛋白丝在蔗糖梯度共分离。当用Triton X-100提取分离的血小板质膜时,肌动蛋白,肌动蛋白结合蛋白和GP Ib被作为Triton X-100残留物回收。这些研究表明,未刺激的血小板含有由肌动蛋白丝和肌动蛋白结合蛋白组成的膜骨架,该骨架不同于其余的细胞骨架,并附着于GP Ib,GP Ia和质膜上的250,000 Mr的次要糖蛋白。

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