NMR off-resonance R1Ď? relaxation dispersion measurements on base carbon and nitrogen nuclei have revealed that wobble G·T/U mismatches in DNA and RNA duplexes exist in dynamic equilibrium with short-lived, low-abundance, and mutagenic Watsonâ??Crick-like conformations. As Watsonâ??Crick-like G·T mismatches have base pairing geometries similar to Watsonâ??Crick base pairs, we hypothesized that they would mimic Watsonâ??Crick base pairs with respect to the sugar-backbone conformation as well. Using off-resonance R1Ď? measurements targeting the sugar C3â?˛ and C4â?˛ nuclei, a structure survey, and molecular dynamics simulations, we show that wobble G·T mismatches adopt sugar-backbone conformations that deviate from the canonical Watsonâ??Crick conformation and that transitions toward tautomeric and anionic Watsonâ??Crick-like G·T mismatches restore the canonical Watsonâ??Crick sugar-backbone. These measurements also reveal kinetic isotope effects for tautomerization in D2O versus H2O, which provide experimental evidence in support of a transition state involving proton transfer. The results provide additional evidence in support of mutagenic Watsonâ??Crick-like G·T mismatches, help rule out alternative inverted wobble conformations in the case of anionic G·Tâ??, and also establish sugar carbons as new non-exchangeable probes of this exchange process.
[NMR paper] Assessment of the Role of TFE Solvent Dynamics in Inducing Conformational Transitions in Melittin: An Approach with Solvent 19F Low Field NMR Relaxation and Overhauser DNP Studies.
Assessment of the Role of TFE Solvent Dynamics in Inducing Conformational Transitions in Melittin: An Approach with Solvent 19F Low Field NMR Relaxation and Overhauser DNP Studies.
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J Phys Chem B. 2020 Jun 23;:
Authors: Chaubey B, Dey A, Banerjee...
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[NMR paper] Probing Conformational Exchange Dynamics in a Short-Lived Protein Folding Intermediate by Real-Time Relaxation-Dispersion NMR.
Probing Conformational Exchange Dynamics in a Short-Lived Protein Folding Intermediate by Real-Time Relaxation-Dispersion NMR.
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J Am Chem Soc. 2017 Jan 11;:
Authors: Franco R, Gil-Caballero S, Ayala I, Favier A, Brutscher B
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NMR spectroscopy is a powerful tool for studying...
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[NMR paper] Probing the Residual Structure of the Low Populated Denatured State of ADA2h under Folding Conditions by Relaxation Dispersion NMR Spectroscopy.
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Biochemistry. 2015 Jun 26;
Authors: Pustovalova Y, Kukic P, Vendruscolo M, Korzhnev DM
Abstract
The structural characterization of low-populated states of proteins with accuracy comparable to that achievable for native states is...
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[NMR paper] Probing the Free Energy Landscape of the Fast-Folding gpW Protein by Relaxation Dispersion NMR.
Probing the Free Energy Landscape of the Fast-Folding gpW Protein by Relaxation Dispersion NMR.
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J Am Chem Soc. 2014 May 8;
Authors: Sanchez-Medina C, Sekhar A, Vallurupalli P, Cerminara M, Muńoz V, Kay LE
Abstract
The topographic features of the free energy landscapes that govern the thermodynamics and kinetics of conformational transitions in proteins, which in turn are integral for function, are not well understood....
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Probing the Free Energy Landscape of the Fast-Folding gpW Protein by Relaxation Dispersion NMR
Probing the Free Energy Landscape of the Fast-Folding gpW Protein by Relaxation Dispersion NMR
Celia Sanchez-Medina, Ashok Sekhar, Pramodh Vallurupalli, Michele Cerminara, Victor Mun?oz and Lewis E. Kay
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Journal of the American Chemical Society
DOI: 10.1021/ja502705y
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[NMR paper] Frontispiece: probing transient conformational States of proteins by solid-state r1? relaxation-dispersion NMR spectroscopy.
Frontispiece: probing transient conformational States of proteins by solid-state r1? relaxation-dispersion NMR spectroscopy.
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Angew Chem Int Ed Engl. 2014 Apr 22;53(17)
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[NMR paper] Probing Transient Conformational States of Proteins by Solid-State R1? Relaxation-Dispersion NMR Spectroscopy.
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Angew Chem Int Ed Engl. 2014 Mar 18;
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Abstract
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Probing Transient HoogsteenHydrogen Bonds in CanonicalDuplex DNA Using NMR Relaxation Dispersion and Single-Atom Substitution
Probing Transient HoogsteenHydrogen Bonds in CanonicalDuplex DNA Using NMR Relaxation Dispersion and Single-Atom Substitution
Evgenia N. Nikolova, Federico L. Gottardo and Hashim M. Al-Hashimi
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Journal of the American Chemical Society
DOI: 10.1021/ja2117816
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