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生成凝血酶作为一种用于探测固体支持物上膜中磷脂混合情况的探针。

Production of thrombin as a probe for mixing of phospholipids in membranes on solid supports.

作者信息

Giesen P L, Hemker H C, Hermens W T

机构信息

Cardiovascular Research Institute Maastricht, University of Limburg, Maastricht, The Netherlands.

出版信息

Biochim Biophys Acta. 1995 Jul 6;1237(1):43-8. doi: 10.1016/0005-2736(95)00109-g.

Abstract

Phospholipid-covered solid supports have been used successfully as model membranes in studies on blood coagulation and other research fields. In order to produce such membranes, simple exposure of the support to suspensions of phospholipid vesicles was recently introduced, but questions have remained about the process of vesicle adherence to the surface and the physico-chemical properties of the resulting membranes. Using a new technique, mixing of phospholipids in such membranes was demonstrated. A rotating, hydrophilic, silicon disc was exposed in a two-step procedure to vesicles prepared from mixtures of dioleoylphosphatidylserine (DOPS) and dioleoylphosphatidylcholine (DOPC). Factor Xa, factor Va and prothrombin were added and the transport-limited production rate of thrombin was measured. For low surface coverage with 40% DOPS/60% DOPC, a much higher conversion rate was found if, prior to addition of coagulation factors, excess DOPC vesicles were added to fill up vacant surface area. It is concluded that DOPS is spread over the entire surface and that confluent bilayers are formed. The presented technique may also be used to measure lateral diffusion constants.

摘要

磷脂覆盖的固体支持物已成功用作血液凝固研究及其他研究领域的模型膜。为了制备此类膜,最近采用了将支持物简单暴露于磷脂囊泡悬浮液的方法,但关于囊泡附着于表面的过程以及所得膜的物理化学性质仍存在疑问。使用一种新技术,证明了此类膜中磷脂的混合情况。将一个旋转的亲水性硅盘分两步暴露于由二油酰磷脂酰丝氨酸(DOPS)和二油酰磷脂酰胆碱(DOPC)混合物制备的囊泡中。加入因子Xa、因子Va和凝血酶原,并测量凝血酶的运输限制产生速率。对于40%DOPS/60%DOPC的低表面覆盖率,如果在添加凝血因子之前加入过量的DOPC囊泡以填充空缺的表面积,则发现转化率要高得多。得出的结论是,DOPS分布在整个表面,形成了融合的双层膜。所提出的技术也可用于测量横向扩散常数。

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