| Literature DB >> 35654846 |
Rob C Oslund1,2, Tamara Reyes-Robles3, Cory H White4, Jake H Tomlinson4, Kelly A Crotty4, Edward P Bowman5, Dan Chang6, Vanessa M Peterson6, Lixia Li6, Silvia Frutos7, Miquel Vila-Perelló7, David Vlerick8, Karen Cromie8, David H Perlman4, Sampat Ingale4, Samantha D O' Hara4, Lee R Roberts4, Grazia Piizzi4, Erik C Hett4, Daria J Hazuda4,9, Olugbeminiyi O Fadeyi10,11.
Abstract
The growing appreciation of immune cell-cell interactions within disease environments has led to extensive efforts to develop immunotherapies. However, characterizing complex cell-cell interfaces in high resolution remains challenging. Thus, technologies leveraging therapeutic-based modalities to profile intercellular environments offer opportunities to study cell-cell interactions with molecular-level insight. We introduce photocatalytic cell tagging (PhoTag) for interrogating cell-cell interactions using single-domain antibodies (VHHs) conjugated to photoactivatable flavin-based cofactors. Following irradiation with visible light, the flavin photocatalyst generates phenoxy radical tags for targeted labeling. Using this technology, we demonstrate selective synaptic labeling across the PD-1/PD-L1 axis in antigen-presenting cell-T cell systems. In combination with multiomics single-cell sequencing, we monitored interactions between peripheral blood mononuclear cells and Raji PD-L1 B cells, revealing differences in transient interactions with specific T cell subtypes. The utility of PhoTag in capturing cell-cell interactions will enable detailed profiling of intercellular communication across different biological systems.Entities:
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Year: 2022 PMID: 35654846 DOI: 10.1038/s41589-022-01044-0
Source DB: PubMed Journal: Nat Chem Biol ISSN: 1552-4450 Impact factor: 16.174