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盘基网柄菌30 kDa肌动蛋白成束蛋白与接触区域的关联。

Association of the Dictyostelium 30 kDa actin bundling protein with contact regions.

作者信息

Fechheimer M, Ingalls H M, Furukawa R, Luna E J

机构信息

Department of Zoology, University of Georgia, Athens.

出版信息

J Cell Sci. 1994 Sep;107 ( Pt 9):2393-401. doi: 10.1242/jcs.107.9.2393.

Abstract

'Contact regions' are plasma membrane domains derived from areas of intercellular contact between aggregating Dictyostelium amebae (H.M. Ingalls et al. (1986). Proc. Nat. Acad. Sci. USA 83, 4779). Purified contact regions contain a prominent actin-binding protein with an M(r) of 34,000. Immunoblotting with monoclonal antibodies identifies this polypeptide as a 34,000 M(r) actin-bundling protein (known as 30 kDa protein), previously shown to be enriched in filopodia (M. Fechheimer (1987). J. Cell Biol. 104, 1539). About four times more 30 kDa protein by mass is associated with contact regions than is found in total plasma membranes isolated from aggregating cells. In agreement with these observations, immunostaining of the 30 kDa protein in aggregating cells reveals a prominent localization along the plasma membrane at sites of intercellular contact. By contrast, alpha-actinin does not appear to be significantly enriched at sites of cell to cell contact. Binding experiments using purified plasma membranes, actin and 30 kDa protein indicate that the 30 kDa protein is associated with the plasma membrane primarily through interactions with actin filaments. Calcium ions are known to decrease the interaction of actin with 30 kDa protein in solution. Surprisingly, membrane-associated complexes of actin and the 30 kDa protein are much less sensitive to dissociation by micromolar levels of free calcium ions than are complexes in solutions lacking membranes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

“接触区域”是指从聚集的盘基网柄菌变形虫之间的细胞间接触区域衍生而来的质膜结构域(H.M.英格尔斯等人,《美国国家科学院院刊》83卷,4779页,1986年)。纯化后的接触区域含有一种显著的肌动蛋白结合蛋白,其相对分子质量为34000。用单克隆抗体进行免疫印迹分析表明,该多肽是一种相对分子质量为34000的肌动蛋白成束蛋白(称为30 kDa蛋白),先前已证明其在丝状伪足中含量丰富(M.费希默,《细胞生物学杂志》104卷,1539页,1987年)。与从聚集细胞中分离得到的总质膜相比,接触区域中按质量计的30 kDa蛋白含量约多四倍。与这些观察结果一致,对聚集细胞中30 kDa蛋白进行免疫染色显示,在细胞间接触部位的质膜上有明显定位。相比之下,α - 辅肌动蛋白在细胞间接触部位似乎没有显著富集。使用纯化的质膜、肌动蛋白和30 kDa蛋白进行的结合实验表明,30 kDa蛋白主要通过与肌动蛋白丝相互作用而与质膜结合。已知钙离子会降低溶液中肌动蛋白与30 kDa蛋白的相互作用。令人惊讶的是,与缺乏膜的溶液中的复合物相比,肌动蛋白和30 kDa蛋白的膜相关复合物对微摩尔浓度的游离钙离子解离的敏感性要低得多。(摘要截选至250词)

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