Cooper J A, Walker S B, Pollard T D
J Muscle Res Cell Motil. 1983 Apr;4(2):253-62. doi: 10.1007/BF00712034.
The fluorescence of pyrene-labelled actin is much higher after polymerization. We have characterized in detail the polymerization properties of pyrene actin and report that native and pyrene actin are identical using the following criteria: (1) the time course of polymerization; (2) the elongation rate constants; (3) the intrinsic viscosity; and (4) the critical concentration. Native and pyrene actin copolymerize. Fluorescence of polymerized pyrene actin is 7-10 times higher than monomer. The fluorescent signal is proportional to polymer weight concentration and is insensitive to filament length distribution. Bleaching can be minimized by appropriate filters to allow continuous monitoring of signal. Measurements do not influence polymerization kinetics. This establishes that pyrene actin fluorescence is a valid assay for actin polymerization that is more sensitive than any other current assay.
芘标记的肌动蛋白聚合后荧光强度会显著增强。我们详细表征了芘肌动蛋白的聚合特性,并依据以下标准报告天然肌动蛋白和芘肌动蛋白是相同的:(1)聚合的时间进程;(2)伸长速率常数;(3)特性粘度;以及(4)临界浓度。天然肌动蛋白和芘肌动蛋白可共聚。聚合后的芘肌动蛋白荧光比单体高7至10倍。荧光信号与聚合物重量浓度成正比,且对细丝长度分布不敏感。通过合适的滤光片可将漂白降至最低,以便持续监测信号。测量不会影响聚合动力学。这表明芘肌动蛋白荧光是一种用于肌动蛋白聚合的有效检测方法,比目前任何其他检测方法都更灵敏。