荧光
秀丽隐杆线虫
斑马鱼
荧光蛋白
绿色荧光蛋白
近红外光谱
生物
荧光显微镜
细胞生物学
生物物理学
蛋白质标签
黄色荧光蛋白
体内
计算生物学
生物化学
融合蛋白
遗传学
神经科学
基因
重组DNA
物理
量子力学
作者
Hanbin Zhang,Stavrini Papadaki,Xiaoting Sun,Li Wang,Mikhail Drobizhev,Luxia Yao,Michel Rehbock,Reinhard W. Köster,Lianfeng Wu,Kazuhiko Namikawa,Kiryl D. Piatkevich
出处
期刊:Nature Methods
[Springer Nature]
日期:2023-09-04
卷期号:20 (10): 1605-1616
被引量:6
标识
DOI:10.1038/s41592-023-01975-z
摘要
Recent progress in fluorescent protein development has generated a large diversity of near-infrared fluorescent proteins (NIR FPs), which are rapidly becoming popular probes for a variety of imaging applications. However, the diversity of NIR FPs poses a challenge for end-users in choosing the optimal one for a given application. Here we conducted a systematic and quantitative assessment of intracellular brightness, photostability, oligomeric state, chemical stability and cytotoxicity of 22 NIR FPs in cultured mammalian cells and primary mouse neurons and identified a set of top-performing FPs including emiRFP670, miRFP680, miRFP713 and miRFP720, which can cover a majority of imaging applications. The top-performing proteins were further validated for in vivo imaging of neurons in Caenorhabditis elegans, zebrafish, and mice as well as in mice liver. We also assessed the applicability of the selected NIR FPs for multicolor imaging of fusions, expansion microscopy and two-photon imaging. This Registered Report describes an extensive comparison of 22 near-infrared fluorescent proteins in vitro, in cultured mammalian cells, and in model animals, clarifying top performers in diverse biological settings.
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