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侧向移动细胞粘附分子的二维解离常数分析

Analysis of two-dimensional dissociation constant of laterally mobile cell adhesion molecules.

作者信息

Zhu De-Min, Dustin Michael L, Cairo Christopher W, Golan David E

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Hematology Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

Biophys J. 2007 Feb 1;92(3):1022-34. doi: 10.1529/biophysj.106.089649. Epub 2006 Nov 3.

Abstract

We formulate a general analysis to determine the two-dimensional dissociation constant (2D Kd), and use this method to study the interaction of CD2-expressing T cells with glass-supported planar bilayers containing fluorescently labeled CD58, a CD2 counter-receptor. Both CD2 and CD58 are laterally mobile in their respective membranes. Adhesion is indicated by accumulation of CD2 and CD58 in the cell-bilayer contact area; adhesion molecule density and contact area size attain equilibrium within 40 min. The standard (Scatchard) analysis of solution-phase binding is not applicable to the case of laterally mobile adhesion molecules due to the dynamic nature of the interaction. We derive a new binding equation, B/F=[(Ntxf)/(KdxScell)]-[(Bxp)/Kd], where B and F are bound and free CD58 density in the contact area, respectively; Nt is CD2 molecule number per cell; f is CD2 fractional mobility; Scell is cell surface area; and p is the ratio of contact area at equilibrium to Scell. We use this analysis to determine that the 2D Kd for CD2-CD58 is 5.4-7.6 molecules/microm2. 2D Kd analysis provides a general and quantitative measure of the mechanisms regulating cell-cell adhesion.

摘要

我们制定了一种通用分析方法来确定二维解离常数(2D Kd),并使用该方法研究表达CD2的T细胞与含有荧光标记的CD58(一种CD2反受体)的玻璃支撑平面双层膜之间的相互作用。CD2和CD58在各自的膜中均可横向移动。细胞双层接触区域中CD2和CD58的积累表明存在粘附;粘附分子密度和接触面积大小在40分钟内达到平衡。由于相互作用的动态性质,溶液相结合的标准(Scatchard)分析不适用于横向移动的粘附分子的情况。我们推导了一个新的结合方程,B/F = [(Ntxf)/(KdxScell)] - [(Bxp)/Kd],其中B和F分别是接触区域中结合和游离的CD58密度;Nt是每个细胞的CD2分子数;f是CD2的分数迁移率;Scell是细胞表面积;p是平衡时接触面积与Scell的比值。我们使用该分析确定CD2 - CD58的2D Kd为5.4 - 7.6个分子/μm²。二维Kd分析为调节细胞 - 细胞粘附的机制提供了一种通用的定量测量方法。

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