TY - JOUR
T1 - Designing Reversible Photoswitching Azobenzene-Modified Nucleotide for Controlling Biological Function
AU - Li, Juncheng
AU - Du, Jinxi
AU - He, Weiwei
AU - Adelakun, Ibrahim O.
AU - Zhong, Miao
AU - Boyer, Savia
AU - Zheng, Ya Ying
AU - Lin, Qishan
AU - Kirmizialtin, Serdal
AU - Sheng, Jia
AU - Wang, Ting
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.
PY - 2025/6/25
Y1 - 2025/6/25
N2 - RNA plays vital roles in numerous normal and diseased cellular functions and processes. Reversible photoregulation of oligonucleotide’s structure and function is a powerful strategy for both regulating biological processes and developing novel RNA-based therapeutics. Herein, we designed an azobenzene-modified cytidine phosphoramidite and synthesized a series of oligoribonucleotides containing this photoswitchable residue. We validated the reversible photoisomerization in both ribonucleoside and oligoribonucleotide contexts and studied the overall impact of this cytidine modification through all-atom molecular dynamics (MD) simulations and UV melting experiments. We also showed that the modified oligoribonucleotide can switch the reverse transcription (RT) process upon light irradiation in the presence of various RT enzymes. In addition, the optical control mechanism of the HIV reverse transcriptase-mediated RT process was elucidated by MD simulation. This new chemical biology toolset enables reversible optical control of RNA structures and functions for gene regulation and novel drug development.
AB - RNA plays vital roles in numerous normal and diseased cellular functions and processes. Reversible photoregulation of oligonucleotide’s structure and function is a powerful strategy for both regulating biological processes and developing novel RNA-based therapeutics. Herein, we designed an azobenzene-modified cytidine phosphoramidite and synthesized a series of oligoribonucleotides containing this photoswitchable residue. We validated the reversible photoisomerization in both ribonucleoside and oligoribonucleotide contexts and studied the overall impact of this cytidine modification through all-atom molecular dynamics (MD) simulations and UV melting experiments. We also showed that the modified oligoribonucleotide can switch the reverse transcription (RT) process upon light irradiation in the presence of various RT enzymes. In addition, the optical control mechanism of the HIV reverse transcriptase-mediated RT process was elucidated by MD simulation. This new chemical biology toolset enables reversible optical control of RNA structures and functions for gene regulation and novel drug development.
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U2 - 10.1021/jacs.5c03252
DO - 10.1021/jacs.5c03252
M3 - Article
C2 - 40513074
AN - SCOPUS:105008384914
SN - 0002-7863
VL - 147
SP - 21638
EP - 21648
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 25
ER -