Affiliation:
1. California Institute of Technology 1 Division of Biology & Biological Engineering , , Pasadena, CA 91125 , USA
2. California Institute of Technology 2 Division of Engineering & Applied Science , , Pasadena, CA 91125 , USA
Abstract
ABSTRACT
Signal amplification based on the mechanism of hybridization chain reaction (HCR) provides a unified framework for multiplex, quantitative, high-resolution imaging of RNA and protein targets in highly autofluorescent samples. With conventional bandpass imaging, multiplexing is typically limited to four or five targets owing to the difficulty in separating signals generated by fluorophores with overlapping spectra. Spectral imaging has offered the conceptual promise of higher levels of multiplexing, but it has been challenging to realize this potential in highly autofluorescent samples, including whole-mount vertebrate embryos. Here, we demonstrate robust HCR spectral imaging with linear unmixing, enabling simultaneous imaging of ten RNA and/or protein targets in whole-mount zebrafish embryos and mouse brain sections. Further, we demonstrate that the amplified and unmixed signal in each of the ten channels is quantitative, enabling accurate and precise relative quantitation of RNA and/or protein targets with subcellular resolution, and RNA absolute quantitation with single-molecule resolution, in the anatomical context of highly autofluorescent samples.
Funder
National Institute of Biomedical Imaging and Bioengineering
National Institute of General Medical Sciences
Beckman Institute, California Institute of Technology
California Institute of Technology
Publisher
The Company of Biologists
Cited by
2 articles.
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