荧光化合物在蛋白质成像应用中的共价标记。

Scanning microscopy. Supplement Pub Date : 1996-01-01
D R Swartz
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引用次数: 0

摘要

用荧光化合物在显微镜下标记蛋白质使得对生物过程有了更深入的了解。荧光蛋白的制备是荧光蛋白在显微镜中应用的第一步。描述了标记和表征蛋白质的方法,作为其他蛋白质的一般方法的示例。用荧光素-5-马来酰亚胺或5-碘乙酰氨基荧光素标记骨骼肌α -肌动蛋白,并对反应进行表征。在一定配比条件下,马来酰亚胺反应比碘乙酰胺反应更快、更有效,偶联效率为65%。对荧光素-5-马来酰亚胺α -肌动蛋白进行了功能表征,荧光素标记对α -肌动蛋白的f -肌动蛋白结合特性基本没有影响。荧光素-肌动素也被证明能特异性地与分离的肌原纤维的z线结合。概述和讨论了如何标记和表征用于显微镜的蛋白质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Covalent labeling of proteins with fluorescent compounds for imaging applications.

The labeling of proteins with fluorescent compounds for microscopy has allowed a greater understanding of biological processes. The preparation of fluorescent proteins is the first step in development of their use in microscopy. Methods are described to label and characterize a protein as an example of the general approach for other proteins. Skeletal muscle alpha-actinin was labeled with either fluorescein-5-maleimide or 5-iodoaceamidofluorescein and the reaction characterized. The maleimide reaction was much more rapid and efficient than the iodoacetamide reaction giving a coupling efficiency of 65% under the given ration conditions. The fluorescein-5-maleimide alpha-actinin was functionally characterized and there was essentially no influence on the fluorescein label on the F-actin binding properties of alpha-actinin. The fluorescein alpha-actinin was also shown to specifically bind to the Z-line of isolated myofibrils. A general outline and discussion are presented on how to label and characterize proteins for use in microscopy.

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