TY - JOUR
T1 - Excited-State Charge Transfer, Proton Transfer, and Exciplex Formation Revealed by Ultrafast Time-Resolved Spectroscopy in Human Telomeric Ribonucleic Acid Quadruplex
AU - Ma, Chensheng
AU - Chow, Joshua Chiu Lok
AU - Wong, Allen Ka Wa
AU - Xiong, Qingwu
AU - Chomchoei, Jacob
AU - Kwok, Wai Ming
N1 - Funding Information:
The authors thank the National Natural Science Foundation of China (Nos. 21773157 and 22073063), the Project of Shenzhen Science and Technology (JCYJ20190808110801662), and the Research Grants Council of Hong Kong (15303018, 15302319, and 15301721) for financial support.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/6/8
Y1 - 2023/6/8
N2 - Guanine quadruplexes (GQs), important for genome stability and biotechnology application, can form from both DNA and RNA. However, unlike the study of DNA GQs, little research has been conducted on excited states of GQs from RNA, which due to the ribose 2′-hydroxy group have structures distinct from their DNA counterparts. Combining ultrafast broadband time-resolved fluorescence and transient absorption measurements, we report the first direct probe of excitation dynamics for a bimolecular GQ from human telomeric repeat-containing RNA taking the typical highly compacted parallel folding with a propeller-like loop structure. The result revealed a multichannel decay containing an unusual high-energy excimer featuring charge transfer deactivated by rapid proton transfer in the tetrad core region. It also identified an unprecedented exciplex displaying massively red-shifted fluorescence produced from charge transfer in the loop region. The findings underscore the role of structural conformation and base content in determining the energy, electronic attribution, and decay dynamics of GQ excited states.
AB - Guanine quadruplexes (GQs), important for genome stability and biotechnology application, can form from both DNA and RNA. However, unlike the study of DNA GQs, little research has been conducted on excited states of GQs from RNA, which due to the ribose 2′-hydroxy group have structures distinct from their DNA counterparts. Combining ultrafast broadband time-resolved fluorescence and transient absorption measurements, we report the first direct probe of excitation dynamics for a bimolecular GQ from human telomeric repeat-containing RNA taking the typical highly compacted parallel folding with a propeller-like loop structure. The result revealed a multichannel decay containing an unusual high-energy excimer featuring charge transfer deactivated by rapid proton transfer in the tetrad core region. It also identified an unprecedented exciplex displaying massively red-shifted fluorescence produced from charge transfer in the loop region. The findings underscore the role of structural conformation and base content in determining the energy, electronic attribution, and decay dynamics of GQ excited states.
UR - http://www.scopus.com/inward/record.url?scp=85162844102&partnerID=8YFLogxK
U2 - 10.1021/acs.jpclett.3c00806
DO - 10.1021/acs.jpclett.3c00806
M3 - Journal article
C2 - 37232555
AN - SCOPUS:85162844102
SN - 1948-7185
VL - 14
SP - 5085
EP - 5094
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 22
ER -