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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