核酸
核糖核酸
点击化学
DNA
荧光原位杂交
杂交探针
荧光
核酸热力学
荧光显微镜
化学
生物物理学
原位杂交
分子生物学
生物
生物化学
组合化学
信使核糖核酸
基序列
基因
染色体
物理
光学
作者
Sara H. Rouhanifard,Ian A. Mellis,Margaret C. Dunagin,Sareh Bayatpour,Connie Jiang,Ian Dardani,Orsolya Symmons,Benjamin Emert,Eduardo A. Torre,Allison Coté,Alessandra M. Sullivan,J Stamatoyannopoulos,Arjun Raj
摘要
Sensitive detection of individual RNA and DNA molecules is achieved by exponentially amplifying the fluorescence signal. Methods for detecting single nucleic acids in cell and tissues, such as fluorescence in situ hybridization (FISH), are limited by relatively low signal intensity and nonspecific probe binding. Here we present click-amplifying FISH (clampFISH), a method for fluorescence detection of nucleic acids that achieves high specificity and high-gain (>400-fold) signal amplification. ClampFISH probes form a 'C' configuration upon hybridization to the sequence of interest in a double helical manner. The ends of the probes are ligated together using bio-orthogonal click chemistry, effectively locking the probes around the target. Iterative rounds of hybridization and click amplify the fluorescence intensity. We show that clampFISH enables the detection of RNA species with low-magnification microscopy and in RNA-based flow cytometry. Additionally, we show that the modular design of clampFISH probes allows multiplexing of RNA and DNA detection, that the locking mechanism prevents probe detachment in expansion microscopy, and that clampFISH can be applied in tissue samples.
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