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Sökning: WFRF:(Duchardt Ferner E) > (2020) > Secondary structure...

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FältnamnIndikatorerMetadata
00004517naa a2201009 4500
001oai:prod.swepub.kib.ki.se:145646070
003SwePub
008240701s2020 | |||||||||||000 ||eng|
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1456460702 URI
024a https://doi.org/10.1093/nar/gkaa10132 DOI
040 a (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Wacker, A4 aut
2451 0a Secondary structure determination of conserved SARS-CoV-2 RNA elements by NMR spectroscopy
264 c 2020-11-10
264 1b Oxford University Press (OUP),c 2020
520 a The current pandemic situation caused by the Betacoronavirus SARS-CoV-2 (SCoV2) highlights the need for coordinated research to combat COVID-19. A particularly important aspect is the development of medication. In addition to viral proteins, structured RNA elements represent a potent alternative as drug targets. The search for drugs that target RNA requires their high-resolution structural characterization. Using nuclear magnetic resonance (NMR) spectroscopy, a worldwide consortium of NMR researchers aims to characterize potential RNA drug targets of SCoV2. Here, we report the characterization of 15 conserved RNA elements located at the 5′ end, the ribosomal frameshift segment and the 3′-untranslated region (3′-UTR) of the SCoV2 genome, their large-scale production and NMR-based secondary structure determination. The NMR data are corroborated with secondary structure probing by DMS footprinting experiments. The close agreement of NMR secondary structure determination of isolated RNA elements with DMS footprinting and NMR performed on larger RNA regions shows that the secondary structure elements fold independently. The NMR data reported here provide the basis for NMR investigations of RNA function, RNA interactions with viral and host proteins and screening campaigns to identify potential RNA binders for pharmaceutical intervention.
700a Weigand, JE4 aut
700a Akabayov, SR4 aut
700a Altincekic, N4 aut
700a Bains, JK4 aut
700a Banijamali, E4 aut
700a Binas, O4 aut
700a Castillo-Martinez, J4 aut
700a Cetiner, E4 aut
700a Ceylan, B4 aut
700a Chiu, LY4 aut
700a Davila-Calderon, J4 aut
700a Dhamotharan, K4 aut
700a Duchardt-Ferner, E4 aut
700a Ferner, J4 aut
700a Frydman, L4 aut
700a Furtig, B4 aut
700a Gallego, J4 aut
700a Grun, JT4 aut
700a Hacker, C4 aut
700a Haddad, C4 aut
700a Hahnke, M4 aut
700a Hengesbach, M4 aut
700a Hiller, F4 aut
700a Hohmann, KF4 aut
700a Hymon, D4 aut
700a de Jesus, V4 aut
700a Jonker, H4 aut
700a Keller, H4 aut
700a Knezic, B4 aut
700a Landgraf, T4 aut
700a Lohr, F4 aut
700a Luo, L4 aut
700a Mertinkus, KR4 aut
700a Muhs, C4 aut
700a Novakovic, M4 aut
700a Oxenfarth, A4 aut
700a Palomino-Schatzlein, M4 aut
700a Petzold, Ku Karolinska Institutet4 aut
700a Peter, SA4 aut
700a Pyper, DJ4 aut
700a Qureshi, NS4 aut
700a Riad, M4 aut
700a Richter, C4 aut
700a Saxena, K4 aut
700a Schamber, T4 aut
700a Scherf, T4 aut
700a Schlagnitweit, J4 aut
700a Schlundt, A4 aut
700a Schnieders, R4 aut
700a Schwalbe, H4 aut
700a Simba-Lahuasi, A4 aut
700a Sreeramulu, S4 aut
700a Stirnal, E4 aut
700a Sudakov, A4 aut
700a Tants, JN4 aut
700a Tolbert, BS4 aut
700a Vogele, J4 aut
700a Weiss, L4 aut
700a Wirmer-Bartoschek, J4 aut
700a Martin, MAW4 aut
700a Wohnert, J4 aut
700a Zetzsche, H4 aut
710a Karolinska Institutet4 org
773t Nucleic acids researchd : Oxford University Press (OUP)g 48:22, s. 12415-12435q 48:22<12415-12435x 1362-4962x 0305-1048
856u https://academic.oup.com/nar/article-pdf/48/22/12415/38817308/gkaa1013.pdf
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:145646070
8564 8u https://doi.org/10.1093/nar/gkaa1013

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