Back to Authors

Byrne, Shane R.

https://orcid.org/0000-0002-2136-305X

Mayo Clinic

Massachusetts Institute of Technology

Citations 2

DNA Modifications Enabling Proximity Biotinylation
Pearson, Keenan , Byrne, Shane R. , Bickart, Laura B., Maher, L. James , Byrne, Shane R , Dedon, Peter C , III, Louis James Maher , Pearson, Keenan S , Wilbanks, Brandon

Bioconjugate Chemistry | March 8, 2023 | Volume: 34 | Issue: 4 | Pages: 611-615

10.1021/acs.bioconjchem.2c00475 Get It

Phenoxy Radical Reactivity of Nucleic Acids: Practical Implications for Biotinylation
Wilbanks, Brandon , Garcia, Brian A., Byrne, Shane R. , Maher, L. James , Garcia, Brian, III, Louis James Maher , Byrne, Shane R , Wilbanks, Brandon A , Dedon, Peter C

ChemBioChem | December 24, 2020 | Volume: 22 | Issue: 8 | Pages: 1400-1404

10.1002/cbic.202000854 Get It

AbstractRecent advances in peroxidase‐mediated biotin tyramide (BT) signal amplification technology have resulted in high‐resolution and subcellular compartment‐specific mapping of protein and RNA localization. Horseradish peroxidase (HRP) in the presence of H2O2 is known to activate phenolic compounds for phenoxy radical reaction with nucleic acids, where biotinylation by BT is a practical example. BT reactivity with RNA and DNA is not understood in detail. We report that BT phenoxy radicals react in a sequence‐independent manner with guanosine bases in RNA. In contrast, DNA reactivity with BT cannot be detected by our methods under the same conditions. Remarkably, we show that fluorescein conjugates DNA rapidly and selectively reacts with BT phenoxy radicals, allowing convenient and practical biotinylation of DNA on fluorescein with retention of fluorescence.