Answers are grounded in this paper and cite their sources.
Experimental study demonstrates rapid RNA structure mapping using a nitrone-based click reagent in human cells, highlighting an efficient tool for bioorthogonal profiling.
We report the synthesis and testing of a new reagent for selective 2′-hydroxyl acylation analyzed by primer extension (SHAPE). We report the synthesis and testing of a nitrone acyl imidazole that is capable of labelling RNA (DMImO-AI) for applications including in vivo click SHAPE (icSHAPE). The new reagent has a reasonable lifetime for in vivo applications and can undergo strain-promoted alkyne-nitrone cycloaddition reactions that more rapidly conjugates labelled RNA than 2-(azidomethyl)nicotinic acid imidazolide (NAI-N 3 ). We show that DMImO-AI is a useful reagent for SHAPE mapping experiments of RNA from A549 cells with a faster reacting nitrone moiety for bioorthogonal conjugation.
No takes yet. Share an insight, caveat, or question.
Josephson et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: