Burkel Brian M, von Dassow George, Bement William M
Department of Zoology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Cell Motil Cytoskeleton. 2007 Nov;64(11):822-32. doi: 10.1002/cm.20226.
Actin filaments (F-actin) are protein polymers that undergo rapid assembly and disassembly and control an enormous variety of cellular processes ranging from force production to regulation of signal transduction. Consequently, imaging of F-actin has become an increasingly important goal for biologists seeking to understand how cells and tissues function. However, most of the available means for imaging F-actin in living cells suffer from one or more biological or experimental shortcomings. Here we describe fluorescent F-actin probes based on the calponin homology domain of utrophin (Utr-CH), which binds F-actin without stabilizing it in vitro. We show that these probes faithfully report the distribution of F-actin in living and fixed cells, distinguish between stable and dynamic F-actin, and have no obvious effects on processes that depend critically on the balance of actin assembly and disassembly.
肌动蛋白丝(F-肌动蛋白)是蛋白质聚合物,它们经历快速组装和解聚,并控制从力产生到信号转导调控等各种各样的细胞过程。因此,对于试图了解细胞和组织如何发挥功能的生物学家来说,F-肌动蛋白成像已成为一个日益重要的目标。然而,大多数用于活细胞中F-肌动蛋白成像的现有方法存在一个或多个生物学或实验缺陷。在这里,我们描述了基于肌动蛋白结合蛋白(Utr-CH)的钙调蛋白同源结构域的荧光F-肌动蛋白探针,其在体外结合F-肌动蛋白但不使其稳定。我们表明,这些探针如实地报告了活细胞和固定细胞中F-肌动蛋白的分布,区分了稳定和动态的F-肌动蛋白,并且对严重依赖肌动蛋白组装和解聚平衡的过程没有明显影响。