Abstract
Fluorogenic sulforhodamine–neomycin conjugates have been designed and synthesized for RNA tagging. Conjugates were fluorescently activated by binding to RNA aptamers and exhibited greater than 250–400 fold enhancement in binding affinity relative to corresponding unconjugated fluorophores.
Original language | English |
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Pages (from-to) | 10034-10036 |
Number of pages | 3 |
Journal | Chemical Communications |
Volume | 48 |
Issue number | 80 |
DOIs | |
State | Published - 12 Sep 2012 |