Hybridization chain reaction enables a unified approach to multiplexed, quantitative, high-resolution immunohistochemistry and in situ hybridization

Maayan Schwarzkopf, Mike C. Liu, S. Schulte, R. Ives, Naeem Husain, Harry M. T. Choi, N. Pierce
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引用次数: 26

Abstract

RNA in situ hybridization (RNA-ISH) based on the mechanism of hybridization chain reaction (HCR) enables multiplexed, quantitative, high-resolution RNA imaging in highly autofluorescent samples including whole-mount vertebrate embryos, thick brain slices, and formalin-fixed paraffin-embedded (FFPE) tissue sections. Here, we extend the benefits of 1-step, multiplexed, quantitative, isothermal, enzyme-free HCR signal amplification to immunohistochemistry (IHC), enabling accurate and precise protein relative quantitation with subcellular resolution in an anatomical context. More-over, we provide a unified framework for simultaneous quantitative protein and RNA imaging with 1-step HCR signal amplification performed for all target proteins and RNAs simultaneously. SUMMARY Signal amplification based on the mechanism of hybridization chain reaction enables multiplexed, quantitative, high-resolution imaging of protein and RNA targets in highly autofluorescent tissues.
杂交链式反应使多路,定量,高分辨率免疫组织化学和原位杂交的统一方法成为可能
基于杂交链反应(HCR)机制的RNA原位杂交(RNA- ish)能够在高度自荧光的样本中进行多路、定量、高分辨率的RNA成像,包括整片脊椎动物胚胎、厚脑切片和福尔马林固定石蜡包埋(FFPE)组织切片。在这里,我们将一步、多路、定量、等温、无酶HCR信号扩增的优势扩展到免疫组织化学(IHC),从而在解剖学背景下实现精确和精确的亚细胞分辨率蛋白质相对定量。此外,我们为同时定量蛋白和RNA成像提供了一个统一的框架,同时对所有目标蛋白和RNA进行一步HCR信号扩增。基于杂交链式反应机制的信号放大技术可以实现高自荧光组织中蛋白和RNA靶点的多路、定量、高分辨率成像。
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