核糖核酸
显微镜
荧光显微镜
显微镜
生物物理学
原位杂交
纳米尺度
分辨率(逻辑)
材料科学
生物
化学
纳米技术
计算生物学
信使核糖核酸
荧光
生物化学
光学
基因
物理
计算机科学
人工智能
作者
Fei Chen,Asmamaw T. Wassie,Allison Coté,Anubhav Sinha,Shahar Alon,Shoh Asano,Evan R Daugharthy,Jae‐Byum Chang,Adam Marblestone,George M. Church,Arjun Raj,Edward S. Boyden
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2016-07-04
卷期号:13 (8): 679-684
被引量:428
摘要
ExFISH extends expansion microscopy to single-molecule RNA imaging, enabling super-resolution imaging of diverse RNAs in cells and tissues on conventional microscopes. The method enables multiplexed imaging of RNA and improved RNA quantitation. The ability to image RNA identity and location with nanoscale precision in intact tissues is of great interest for defining cell types and states in normal and pathological biological settings. Here, we present a strategy for expansion microscopy of RNA. We developed a small-molecule linker that enables RNA to be covalently attached to a swellable polyelectrolyte gel synthesized throughout a biological specimen. Then, postexpansion, fluorescent in situ hybridization (FISH) imaging of RNA can be performed with high yield and specificity as well as single-molecule precision in both cultured cells and intact brain tissue. Expansion FISH (ExFISH) separates RNAs and supports amplification of single-molecule signals (i.e., via hybridization chain reaction) as well as multiplexed RNA FISH readout. ExFISH thus enables super-resolution imaging of RNA structure and location with diffraction-limited microscopes in thick specimens, such as intact brain tissue and other tissues of importance to biology and medicine.
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