MATE-Seq: microfluidic antigen-TCR engagement sequencing.


Journal

Lab on a chip
ISSN: 1473-0189
Titre abrégé: Lab Chip
Pays: England
ID NLM: 101128948

Informations de publication

Date de publication:
10 09 2019
Historique:
entrez: 11 9 2019
pubmed: 11 9 2019
medline: 2 10 2020
Statut: ppublish

Résumé

Adaptive immunity is based on peptide antigen recognition. Our ability to harness the immune system for therapeutic gain relies on the discovery of the T cell receptor (TCR) genes that selectively target antigens from infections, mutated proteins, and foreign agents. Here we present a method that selectively labels peptide antigen-specific CD8+ T cells using magnetic nanoparticles functionalized with peptide-MHC tetramers, isolates these specific cells within an integrated microfluidic device, and directly amplifies the TCR genes for sequencing. Critically, the identity of the peptide recognized by the TCR is preserved, providing the link between peptide and gene. The platform requires inputs on the order of just 100 000 CD8+ T cells, can be multiplexed for simultaneous analysis of multiple peptides, and performs sorting and isolation on chip. We demonstrate 1000-fold sensitivity enhancement of detecting antigen-specific TCRs relative to bulk analysis and simultaneous capture of two virus antigen-specific TCRs from a population of T cells.

Identifiants

pubmed: 31502632
doi: 10.1039/c9lc00538b
doi:

Substances chimiques

Antigens 0
Magnetite Nanoparticles 0
Receptors, Antigen, T-Cell 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3011-3021

Subventions

Organisme : NCI NIH HHS
ID : F32 CA213966
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA199090
Pays : United States

Auteurs

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Classifications MeSH