| Literature DB >> 31397326 |
Robert J Trachman1, Jason R Stagno2, Chelsie Conrad2, Christopher P Jones1, Pontus Fischer3, Alke Meents3, Yun Xing Wang2, Adrian R Ferré-D'Amaré1.
Abstract
Turn-on aptamers are in vitro-selected RNAs that bind to conditionally fluorescent small molecules and enhance their fluorescence. Upon binding TO1-biotin, the iMango-III aptamer achieves the largest fluorescence enhancement reported for turn-on aptamers (over 5000-fold). This aptamer was generated by structure-guided engineering and functional reselection of the parental aptamer Mango-III. Structures of both Mango-III and iMango-III have previously been determined by conventional cryocrystallography using synchrotron X-radiation. Using an X-ray free-electron laser (XFEL), the room-temperature iMango-III-TO1-biotin co-crystal structure has now been determined at 3.0 Å resolution. This structural model, which was refined against a data set of ∼1300 diffraction images (each from a single crystal), is largely consistent with the structures determined from single-crystal data sets collected at 100 K. This constitutes a technical benchmark on the way to XFEL pump-probe experiments on fluorescent RNA-small molecule complexes.Entities:
Keywords: RNA structure; X-ray free-electron lasers; XFELS; fluorescence; fluorescence turn-on aptamers; iMango-III; room temperature
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Year: 2019 PMID: 31397326 PMCID: PMC6688663 DOI: 10.1107/S2053230X19010136
Source DB: PubMed Journal: Acta Crystallogr F Struct Biol Commun ISSN: 2053-230X Impact factor: 1.056