| Literature DB >> 28762271 |
Wei Du, Hui Wang, Yingzhong Zhu, Xiaohe Tian, Mingzhu Zhang, Qiong Zhang, Senio Campos De Souza1, Aidong Wang2, Hongping Zhou, Zhongping Zhang, Jieying Wu, Yupeng Tian.
Abstract
A two-photon fluorescent probe (J1) that selectively stains intracellular nucleolar RNA was screened from three water-soluble terpyridine derivatives (J1-J3) with quaternary ammonium groups. The photophysical properties of J1-J3 were systemically investigated both experimentally and theoretically, revealing that J1-J3 possess large Stokes shifts and the two-photon absorption action cross sections range from 38 to 97 GM in the near-infrared region. This indicates that J1 could specifically stain nucleoli by targeting the nucleolar rRNA from the recognition experiments in vitro, the two-photon imaging experiments, and the stimulated emission depletion in vivo. The mechanism of action in which J1 binds to the nucleolar rRNA was researched via both experiments and molecular modeling. The high binding selectivity of J1 to nucleolar RNA over cytosolic RNA made this probe a potential candidate to visualize rRNA probe in the living cells.Entities:
Keywords: STED; molecular docking techniques; rRNA; two-photon; water-soluble
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Year: 2017 PMID: 28762271 DOI: 10.1021/acsami.7b08068
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229