Demonstrates enhanced protein-protein interaction studies using tunable proximity labeling.
H serves as a quencher during the proximity labeling reaction, and adjusting quencher concentration can attenuate labeling, as demonstrated in vitro on a model protein. Tuning the half-life of the proximity labeling reaction was also studied in live cells to give proteomic data sets with high overlap. Labeling reactions with shorter half-lives enriched fewer total proteins but maintained enrichment of known interactors. We anticipate that this use of fast bioorthogonal reactions will be broadly applicable for studying protein-protein interactions.
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Scinto et al. (2026) studied this question.
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