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快速诱导和分离粘着斑复合物

Rapid induction and isolation of focal adhesion complexes.

作者信息

Plopper G, Ingber D E

机构信息

Department of Surgery, Children's Hospital, Boston, MA 02115.

出版信息

Biochem Biophys Res Commun. 1993 Jun 15;193(2):571-8. doi: 10.1006/bbrc.1993.1662.

Abstract

Focal adhesion complexes (FACs) containing integrin beta 1, talin, vinculin, talin, alpha-actinin, and paxillin formed within 15 min when round cells bound magnetic microbeads coated with integrin ligands, such as fibronectin or RGD-containing peptide, but not when coated with acetylated-low density lipoprotein. Newly formed FACs were isolated and collected for biochemical analysis using a combination of detergent extraction, sonication, dounce homogenization, and magnetic pelleting. Isolated bead complexes were greatly enriched for all FAC proteins when compared with either the whole cytoskeleton or basal cell membranes whereas actin (a general cytoskeletal marker) was relatively depleted. This method which permits isolation of intact FACs within minutes following integrin ligation should facilitate analysis of both FAC assembly and the molecular basis of integrin signaling.

摘要

当圆形细胞与包被有整合素配体(如纤连蛋白或含RGD肽)的磁性微珠结合时,含整合素β1、踝蛋白、纽蛋白、α -辅肌动蛋白和桩蛋白的粘着斑复合物(FACs)在15分钟内形成,但与包被乙酰化低密度脂蛋白的微珠结合时则不会形成。新形成的FACs通过去污剂提取、超声处理、玻璃匀浆和磁性沉淀相结合的方法进行分离和收集,用于生化分析。与整个细胞骨架或基底细胞膜相比,分离出的珠复合物中所有FAC蛋白都得到了极大富集,而肌动蛋白(一种一般的细胞骨架标记物)则相对减少。这种在整合素连接后几分钟内就能分离完整FACs的方法,应该有助于对FAC组装以及整合素信号传导的分子基础进行分析。

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