荧光
荧光显微镜
荧光蛋白
亮度
显微镜
生物物理学
单体
计算机科学
化学
生物系统
纳米技术
计算生物学
材料科学
绿色荧光蛋白
生物
聚合物
生物化学
光学
物理
基因
有机化学
作者
Paula J. Cranfill,Brittney Sell,Michelle A. Baird,John R. Allen,Zeno Lavagnino,H. Martijn de Gruiter,Gert‐Jan Kremers,Michael W. Davidson,Alessandro Ustione,David W. Piston
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2016-05-30
卷期号:13 (7): 557-562
被引量:480
摘要
The advent of fluorescent proteins (FPs) for genetic labeling of molecules and cells has revolutionized fluorescence microscopy. Genetic manipulations have created a vast array of bright and stable FPs spanning blue to red spectral regions. Common to autofluorescent FPs is their tight β-barrel structure, which provides the rigidity and chemical environment needed for effectual fluorescence. Despite the common structure, each FP has unique properties. Thus, there is no single 'best' FP for every circumstance, and each FP has advantages and disadvantages. To guide decisions about which FP is right for a given application, we have quantitatively characterized the brightness, photostability, pH stability and monomeric properties of more than 40 FPs to enable straightforward and direct comparison between them. We focus on popular and/or top-performing FPs in each spectral region.
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