High-throughput single-cell proteomics and transcriptomics from same cells with a nanoliter-scale, spin-transfer approach

Read full text
Authors: Pranav Dawar, Lye Meng Markillie, Sarah M Williams, Hugh D. Mitchell, Johannes W Bagnoli, Joshua Cantlon-Bruce, Anjali Seth, Carter C. Bracken, ljiljana Pasa-Tolic, Ying Zhu, James Michael Fulcher
Cited by: 1
References: 35

Abstract

a centrifugation-based approach, while proteins are retained on the initial platform. Benchmarking of nanoSPINS on two cell lines demonstrates its ability to generate global proteomic and transcriptomic profiles that align well with previously established methodologies/platforms. The incorporation of isobaric TMTpro labeling into this single-cell multiomics platform significantly enhances the throughput of single-cell proteomic analyses. Through the high-throughput quantification of the proteome and transcriptome, nanoSPINS not only facilitates the identification of molecular features at both mRNA and protein level but also provides larger sample sizes for improved statistical power in clustering and differential abundance. Given the broad applicability of single-cell multiomics in biological research and clinical settings, we believe nanoSPINS represents a powerful platform for the characterization of heterogeneous cell populations.

Fields of Study & Subjects

Single-cell and spatial transcriptomics Advanced Biosensing Techniques and Applications Advanced biosensing and bioanalysis techniques

Publication details

Journal / source
Lab on a Chip
Publisher
Royal Society of Chemistry (RSC)
Volume
26
Issue
7
Pages
2319–2329
Publication date
1 January 2026
Language
EN