| Literature DB >> 33585449 |
Renjie Liao1, Manas Mondal1, Christopher D Nazaroff1,2, Diego Mastroeni3,4, Paul D Coleman3,4, Joshua Labaer1, Jia Guo1.
Abstract
The ability to comprehensively profile proteins in intact tissues in situ is crucial for our understanding of health and disease. However, the existing methods suffer from low sensitivity and limited sample throughput. To address these issues, here we present a highly sensitive and multiplexed in situ protein analysis approach using cleavable fluorescent tyramide and off-the-shelf antibodies. Compared with the current methods, this approach enhances the detection sensitivity and reduces the imaging time by 1-2 orders of magnitude, and can potentially detect hundreds of proteins in intact tissues at the optical resolution. Applying this approach, we studied protein expression heterogeneity in a population of genetically identical cells, and performed protein expression correlation analysis to identify co-regulated proteins. We also profiled >6,000 neurons in a human formalin-fixed paraffin-embedded (FFPE) hippocampus tissue. By partitioning these neurons into varied cell clusters based on their multiplexed protein expression profiles, we observed different sub-regions of the hippocampus consist of neurons from distinct clusters.Entities:
Keywords: hippocampus; immunofluorescence; immunohistochemistry; single-cell; spatial proteomics
Year: 2021 PMID: 33585449 PMCID: PMC7874177 DOI: 10.3389/fcell.2020.614624
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X