Complementary-addressed site-directed spin labeling of long natural RNAs Full article
Journal |
Nucleic Acids Research
ISSN: 0305-1048 , E-ISSN: 1362-4962 |
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Output data | Year: 2016, Volume: 44, Number: 16, Pages: 7935-7943 Pages count : 9 DOI: 10.1093/nar/gkw516 | ||||||||||
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Abstract:
Nanoscale distance measurements by pulse dipolar Electron paramagnetic resonance (EPR) spectroscopy allow new insights into the structure and dynamics of complex biopolymers. EPR detection requires site directed spin labeling (SDSL) of biomolecule(s), which remained challenging for long RNAs up-to-date. Here, we demonstrate that novel complementary-addressed SDSL approach allows efficient spin labeling and following structural EPR studies of long RNAs. We succeeded to spin-label Hepatitis C Virus RNA internal ribosome entry site consisting of a parts per thousand 330 nucleotides and having a complicated spatial structure. Application of pulsed double electron-electron resonance provided spin-spin distance distribution, which agrees well with the results of molecular dynamics (MD) calculations. Thus, novel SDSL approach in conjunction with EPR and MD allows structural studies of long natural RNAs with nanometer resolution and can be applied to systems of biological and biomedical significance.
Cite:
Babaylova E.S.
, Malygin A.A.
, Lomzov A.A.
, Pyshnyi D.V.
, Yulikov M.
, Jeschke G.
, Krumkacheva O.A.
, Fedin M.V.
, Karpova G.G.
, Bagryanskaya E.G.
Complementary-addressed site-directed spin labeling of long natural RNAs
Nucleic Acids Research. 2016. V.44. N16. P.7935-7943. DOI: 10.1093/nar/gkw516 WOS Scopus РИНЦ
Complementary-addressed site-directed spin labeling of long natural RNAs
Nucleic Acids Research. 2016. V.44. N16. P.7935-7943. DOI: 10.1093/nar/gkw516 WOS Scopus РИНЦ
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Dates:
Published online: | Jun 6, 2016 |
Published print: | Sep 19, 2016 |
Identifiers:
Web of science | WOS:000384687000037 |
Scopus | 2-s2.0-84988934376 |
Elibrary | 27569813 |
OpenAlex | W2418895284 |