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NMR Titration Studies in Z-DNA Dynamics

Authors
Choi, S.-R.Oh, K.-I.Seo, Y.-J.Lee, J.-H.
Issue Date
Mar-2023
Publisher
Humana Press, Inc.
Keywords
Chemical shift perturbation; DNA–protein interaction; Dynamics; NMR; Titration; Z-DNA; Z-DNA-binding protein
Citation
Methods in molecular biology (Clifton, N.J.), v.2651, pp 69 - 83
Pages
15
Indexed
SCOPUS
Journal Title
Methods in molecular biology (Clifton, N.J.)
Volume
2651
Start Page
69
End Page
83
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/30803
DOI
10.1007/978-1-0716-3084-6_5
ISSN
1064-3745
Abstract
Chemical shift perturbation (CSP) is a simple NMR technique for studying the DNA binding of proteins. Titration of the unlabeled DNA into the 15N-labeled protein is monitored by acquiring a two-dimensional (2D) heteronuclear single-quantum correlation (HSQC) spectrum at each step of the titration. CSP can also provide information on the DNA-binding dynamics of proteins, as well as protein-induced conformational changes in DNA. Here, we describe the titration of DNA for the 15N-labeled Z-DNA-binding protein, monitored via 2D HSQC spectra. NMR titration data can be analyzed with the active B–Z transition model to provide the protein-induced B–Z transition dynamics of DNA. © 2023, The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
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