Literature DB >> 31743557

Detecting Counterion Dynamics in DNA-Protein Association.

Channing C Pletka1, Ridvan Nepravishta1, Junji Iwahara1.   

Abstract

Due to a high density of negative charges on its surface, DNA condenses cations as counterions, forming the so-called "ion atmosphere". Although the release of counterions upon DNA-protein association has been postulated to have a major contribution to the binding thermodynamics, this release remains to be confirmed through a direct observation of the ions. Herein, we report the characterization of the ion atmosphere around DNA using NMR spectroscopy and directly detect the release of counterions upon DNA-protein association. NMR-based diffusion data reveal the highly dynamic nature of counterions within the ion atmosphere around DNA. Counterion release is observed as an increase in the apparent ionic diffusion coefficient, which directly provides the number of counterions released upon DNA-protein association.
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  DNA recognition; NMR spectroscopy; dynamics; ion pairs; protein-DNA interactions

Mesh:

Substances:

Year:  2019        PMID: 31743557      PMCID: PMC6980997          DOI: 10.1002/anie.201910960

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  20 in total

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Authors:  J Reuben; M Shporer; E J Gabbay
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8.  Direct observation of the ion-pair dynamics at a protein-DNA interface by NMR spectroscopy.

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7.  Accurate Machine Learning Prediction of Protein Circular Dichroism Spectra with Embedded Density Descriptors.

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8.  Direct Measurement of Interhelical DNA Repulsion and Attraction by Quantitative Cross-Linking.

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9.  De novo determination of near-surface electrostatic potentials by NMR.

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