The ULTIMATE Reagent: A Universal Photocleavable and Clickable Reagent for the Regiospecific and Reversible End Labeling of Any Nucleic Acid
- 27 April 2018
- journal article
- research article
- Published by Wiley in ChemBioChem
- Vol. 19 (12) , 1264-1270
Abstract
There is a need for methods to chemically incorporate photocleavable labels into synthetic and biologically sourced nucleic acids in a chemically defined and reversible manner. We have previously demonstrated that the light‐cleaved diazo di‐methoxy nitro phenyl ethyl (diazo‐DMNPE) group has a remarkable regiospecificity for modifying terminally phosphorylated siRNA. Building on this observation, we have identified conditions under which a diazo‐DMNPE reagent that we designed (diazo‐DMNPE‐azide or DDA) is able to singly modify any nucleic acid (RNA, DNA, single‐stranded, double‐stranded, 3′ or 5′ phosphate). It can then be modified with any clickable reagent to incorporate arbitrary labels such as fluorophores into the nucleic acid. Finally, native nucleic acid can be regenerated directly through photolysis of the reagent. Use of the described approach should allow for the tagging of any nucleic acid, from any source—natural or unnatural—while allowing for the light‐induced regeneration of native nucleic acid.Keywords
Funding Information
- Directorate for Mathematical and Physical Sciences (1052871)
This publication has 36 references indexed in Scilit:
- A Covalent Approach for Site‐Specific RNA Labeling in Mammalian CellsAngewandte Chemie, 2015
- A Covalent Approach for Site‐Specific RNA Labeling in Mammalian CellsAngewandte Chemie International Edition, 2015
- Click Chemistry Based Functionalizations of Nucleoside, Nucleotide and Nucleic AcidsCurrent Organic Chemistry, 2013
- Click Nucleic Acid Ligation: Applications in Biology and NanotechnologyAccounts of Chemical Research, 2012
- Cleavable linkers in chemical biologyBioorganic & Medicinal Chemistry, 2012
- Imaging of RNA in live cellsCurrent Opinion in Chemical Biology, 2011
- Developing Visible Fluorogenic ‘Click-On’ Dyes for Cellular ImagingBioconjugate Chemistry, 2011
- RNA labeling, conjugation and ligationMethods, 2011
- Click Chemistry for Rapid Labeling and Ligation of RNAChemBioChem, 2010
- Site-directed genome modification: nucleic acid and protein modules for targeted integration and gene correctionTrends in Biotechnology, 2005