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人血浆蛋白诱导小的球形脂质体包封于较大的松弛脂质体中。

Encapsulation of small spherical liposome into larger flaccid liposome induced by human plasma proteins.

作者信息

Pavlic J I, Mares T, Bester J, Jansa V, Daniel M, Iglic A

机构信息

University College of Health Care, University of Ljubljana, Ljubljana, Slovenia.

出版信息

Comput Methods Biomech Biomed Engin. 2009 Apr;12(2):147-50. doi: 10.1080/10255840903081180.

Abstract

We show that human plasma can induce the encapsulation of small spherical liposomes into larger flaccid liposomes. To explain the observed phenomena, it is proposed that the orientational ordering of charged plasma proteins induces attractive interaction between two like-charged liposome surfaces in close contact. It is observed that the encapsulation of the spherical liposome is possible only if the membrane of the target liposome is flexible enough to adapt its shape to the shape of the spherical liposome. In the theoretical model, the shapes of the two agglutinated liposomes are determined by minimisation of the sum of the adhesion energy and the membrane elastic energy. In the simulations, the membrane of liposomes is considered as an elastic structure and discretised via the finite element method using spring elements. It is shown that the observed agglutination of liposomes and encapsulation of smaller spherical liposomes into larger flaccid liposomes may be explained as a competition between the membrane deformation energy and the membrane adhesion energy.

摘要

我们表明,人血浆可诱导小球形脂质体被包裹进更大的松弛脂质体中。为解释所观察到的现象,有人提出带电血浆蛋白的取向有序性会在紧密接触的两个带同种电荷的脂质体表面之间诱导产生吸引相互作用。据观察,只有当靶脂质体的膜足够柔韧以使其形状适应球形脂质体的形状时,球形脂质体的包裹才有可能。在理论模型中,两个凝集脂质体的形状由粘附能和膜弹性能之和的最小化来确定。在模拟中,脂质体的膜被视为一种弹性结构,并通过使用弹簧单元的有限元方法进行离散化。结果表明,所观察到的脂质体凝集以及较小球形脂质体被包裹进更大的松弛脂质体中,可解释为膜变形能与膜粘附能之间的竞争。

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