Aug 2026· Proceedings of the National Academy of Sciences of the United States of America· Vol 123· 0 citations· 13 references
Medicine
TL;DR
This work used isolated brain vascular fragments to study the blood–brain barrier and applied a combination of deep bulk proteomic analysis, a proteomic ruler approach, and scRNA-seq, assuming a high within-gene correlation between mRNA and protein.
Abstract
Current methods for assessing low-abundance proteins in individual cells are limited. As a result, cell functions are often inferred from single-cell RNA sequencing (scRNA-seq) data, which can be misleading due to the poor cross-gene correlation (different genes in the same cells) between messenger RNA (mRNA) and protein levels. To address this issue, we used isolated brain vascular fragments to study the blood–brain barrier. We applied a combination of deep bulk proteomic analysis, a proteomic ruler approach, and scRNA-seq, assuming a high within-gene correlation (same gene in different cells) between mRNA and protein. This approach allowed us to estimate protein copy numbers per cell for 9,940 proteins across eight cell types, including endothelium, smooth muscle, pericytes, fibroblasts, and microglia. We also evaluated protein abundance in astrocyte end-feet attached to the vessel fragments. Our data are available through an Online Database, providing a searchable resource and reference protein atlas for future studies of neurovascular proteomics in health and disease.
The first human single-cell proteomic atlas of the aorta is established, altered FBN1 protein regulation in both human and mouse MFS is revealed, and single-cell proteomics is position as a transformative framework for decoding vascular plasticity and identifying actionable effectors in disease.
Junedh M. Amrute, Lihua Jiang, Nikhita Bolar et al.· Arteriosclerosis, Thrombosis...· 0 citations
A reference-informed Bayesian deconvolution framework and a score that identifies gene–cell-type pairs likely to have more accurate estimates of cross-sample variation are described and shown that observable information can help prioritize pairs with more accurately recovered cross-sample variation.
VINE-seq provides a robust, reproducible workflow for the enrichment and high-resolution profiling of vascular, perivascular, and immune cells from fresh or frozen human and mouse brain tissue and optimized extraction of nuclei from purified vessels using enzymatic digestion.
J. Oberhauser, Bella Ding, M. Reid et al.· Nature Protocols· 0 citations
Spatially resolved protein expression is essential for understanding tissue organization, cellular specialization, and protein function. The open‐access Human Protein Atlas database (www.proteinatlas.org) has generated an extensive antibody‐based tissue resource for a majority of the human protein‐coding genes using co...
Borbala Katona, Rutger Schutten, Filippa Bertilsson et al.· Protein Science· 0 citations
A scalable, cell-type-resolved in vivo CRISPR interference (CRISPRi) platform enabling systematic gene function profiling in the mouse brain is developed and the CRISPRinvivo data portal is established as a community resource for in vivo screening.
Risheng Lin, Ze-Ting Ke, Jian-Hui Wang et al.· Neuron· 0 citations
A single-cell multiomics atlas of the human pancreas is presented, profiling over four million cells and nuclei from 57 donors across fetal development, adult homeostasis, and type 2 diabetes.
E. Mereu, D. Balboa, J. Liebig et al.· Cell Metabolism· 1 citation
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