荧光
抗原
脚手架
化学
细胞生物学
支架蛋白
荧光蛋白
计算生物学
绿色荧光蛋白
生物物理学
纳米技术
生物
生物化学
材料科学
计算机科学
信号转导
光学
基因
遗传学
数据库
物理
作者
Olena S. Oliinyk,Mikhail Baloban,Charles L. Clark,Erin M. Carey,Sergei Pletnev,Axel Nimmerjahn,Vladislav V. Verkhusha
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2022-05-23
卷期号:19 (6): 740-750
被引量:62
标识
DOI:10.1038/s41592-022-01467-6
摘要
Small near-infrared (NIR) fluorescent proteins (FPs) are much needed as protein tags for imaging applications. We developed a 17 kDa NIR FP, called miRFP670nano3, which brightly fluoresces in mammalian cells and enables deep-brain imaging. By exploring miRFP670nano3 as an internal tag, we engineered 32 kDa NIR fluorescent nanobodies, termed NIR-Fbs, whose stability and fluorescence strongly depend on the presence of specific intracellular antigens. NIR-Fbs allowed background-free visualization of endogenous proteins, detection of viral antigens, labeling of cells expressing target molecules and identification of double-positive cell populations with bispecific NIR-Fbs against two antigens. Applying NIR-Fbs as destabilizing fusion partners, we developed molecular tools for directed degradation of targeted proteins, controllable protein expression and modulation of enzymatic activities. Altogether, NIR-Fbs enable the detection and manipulation of a variety of cellular processes based on the intracellular protein profile.
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