Miller K G, Alberts B M
Department of Biochemistry and Biophysics, University of California, San Francisco 94143-0448.
Proc Natl Acad Sci U S A. 1989 Jul;86(13):4808-12. doi: 10.1073/pnas.86.13.4808.
We have developed stable and easy to use filamentous actin (F-actin) affinity-chromatography columns that selectively purify proteins that bind to actin filaments from cell extracts. Most traditional assays for actin-associated proteins screen for their effects on actin polymerization or actin filament crosslinking. Because our technique requires only actin-filament binding, it can identify additional types of proteins involved in the function of the actin cytoskeleton. By chromatographing extracts of several types of cells on these columns, we show that known actin-binding proteins are selectively retained as a subset of a larger group of actin-binding proteins that have not been identified previously.
我们开发了稳定且易于使用的丝状肌动蛋白(F-肌动蛋白)亲和色谱柱,该色谱柱可从细胞提取物中选择性地纯化与肌动蛋白丝结合的蛋白质。大多数针对肌动蛋白相关蛋白的传统检测方法是筛选它们对肌动蛋白聚合或肌动蛋白丝交联的影响。由于我们的技术仅需要肌动蛋白丝结合,因此它可以识别参与肌动蛋白细胞骨架功能的其他类型蛋白质。通过在这些色谱柱上对几种类型细胞的提取物进行层析,我们发现已知的肌动蛋白结合蛋白被选择性地保留为一大组先前未被鉴定的肌动蛋白结合蛋白的一个子集。