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通过长程排斥力和短程吸引力的相互作用实现粘附诱导的结构域形成:模型膜研究

Adhesion-induced domain formation by interplay of long-range repulsion and short-range attraction force: a model membrane study.

作者信息

Albersdörfer A, Feder T, Sackmann E

机构信息

Physics Department, Technische Universität München, Germany.

出版信息

Biophys J. 1997 Jul;73(1):245-57. doi: 10.1016/S0006-3495(97)78065-2.

Abstract

We study the role of the interplay of specific and universal forces for the adhesion of giant vesicles on solid supported membranes. To model the situation of cell adhesion, we incorporated lipopolymers (phospholipids with polyethyleneoxide headgroups) as artificial glycocalix, whereas attractive lock-and-key forces are mimicked by incorporating biotinylated lipids into both membranes and by mediating the strong coupling through streptavidin. Adhesion is studied by quantitative reflection interference contrast microscopy (RICM), which enables visualization of the contact zone and reconstruction of the height profile of the membrane beyond the contact line (outside the contact zone) up to a height of 1 micron. We demonstrate that adhesion is accompanied by lateral phase separation, leading to the formation of domains of tight adhesion (adhesion plaques) separated by areas of weak adhesion exhibiting pronounced flickering. By analyzing the height profile S(x) near the contact line in terms of the tension equilibrium (Young equation) and the moment equilibrium, respectively, the adhesion energy and membrane tension can be approximately measured locally. We show that the adhesion energy is about three orders of magnitude larger for the adhesion plaques than for the weekly adhering regions. The adhesion is studied as a function of the excess area of the vesicle generated by temperature variation. A very remarkable finding is that increased excess area is not always stored in the contact area, but leads to the formation of microbuds (diameter approximately 2 microns).

摘要

我们研究了特定力和普遍力的相互作用在巨型囊泡与固体支撑膜黏附中所起的作用。为了模拟细胞黏附的情况,我们将脂聚合物(带有聚环氧乙烷头部基团的磷脂)作为人工糖萼引入,而通过将生物素化脂质掺入两种膜中并通过链霉亲和素介导强耦合来模拟有吸引力的锁钥力。通过定量反射干涉对比显微镜(RICM)研究黏附情况,该显微镜能够可视化接触区域,并重建接触线之外(接触区域之外)高达1微米高度的膜的高度轮廓。我们证明黏附伴随着横向相分离,导致形成紧密黏附区域(黏附斑),这些区域由表现出明显闪烁的弱黏附区域分隔开。通过分别根据张力平衡(杨氏方程)和力矩平衡分析接触线附近的高度轮廓S(x),可以局部近似测量黏附能和膜张力。我们表明,黏附斑的黏附能比弱黏附区域大约大三个数量级。研究了黏附作为温度变化产生的囊泡多余面积的函数。一个非常显著的发现是,增加的多余面积并不总是存储在接触区域,而是导致形成微芽(直径约2微米)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee7/1180926/9e119f555b72/biophysj00032-0255-a.jpg

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