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绿色荧光蛋白单分子的开/关闪烁及转换行为

On/off blinking and switching behaviour of single molecules of green fluorescent protein.

作者信息

Dickson R M, Cubitt A B, Tsien R Y, Moerner W E

机构信息

Department of Chemistry and Biochemistry, University of California San Diego, La Jolla 92093-0340, USA.

出版信息

Nature. 1997 Jul 24;388(6640):355-8. doi: 10.1038/41048.

Abstract

Optical studies of individual molecules at low and room temperature can provide information about the dynamics of local environments in solids, liquids and biological systems unobscured by ensemble averaging. Here we present a study of the photophysical behaviour of single molecules of the green fluorescent protein (GFP) derived from the jellyfish Aequorea victoria. Wild-type GFP and its mutant have attracted interest as fluorescent biological labels because the fluorophore may be formed in vivo. GFP mutants immobilized in aereated aqueous polymer gels and excited by 488-nm light undergo repeated cycles of fluorescent emission ('blinking') on a timescale of several seconds-behaviour that would be unobservable in bulk studies. Eventually the individual GFP molecules reach a long-lasting dark state, from which they can be switched back to the original emissive state by irradiation at 405 nm. This suggests the possibility of using these GFPs as fluorescent markers for time-dependent cell processes, and as molecular photonic switches or optical storage elements, addressable on the single-molecule level.

摘要

在低温和室温下对单个分子进行光学研究,可以提供有关固体、液体和生物系统中局部环境动力学的信息,而不受系综平均的影响。在此,我们展示了对源自维多利亚多管水母的绿色荧光蛋白(GFP)单分子的光物理行为的研究。野生型GFP及其突变体作为荧光生物标记物引起了人们的兴趣,因为荧光团可以在体内形成。固定在充气水性聚合物凝胶中并用488纳米光激发的GFP突变体,在几秒钟的时间尺度上经历重复的荧光发射循环(“闪烁”)——这种行为在整体研究中是无法观察到的。最终,单个GFP分子会进入一个持久的暗态,通过405纳米的照射可以将它们切换回原来的发射态。这表明了将这些GFP用作时间依赖性细胞过程的荧光标记物,以及用作单分子水平上可寻址的分子光子开关或光存储元件的可能性。

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