Nucleic Acids ResearchBiophysicsPeer-reviewed journal article
Zα and Zβ domains of ADAR1 and ZBP1 bind to G-quadruplexes with low micromolar affinity
Charles W. KroftiD, Jeffrey B. KralliD, Magda Warchol, Robb S. WeltyiD, Alan G. HerbertiD, Morkos A. HeneniD, Beat VögeliiD
Abstract
1While it is well established that the Z domains of ADAR1 and ZBP1 proteins bind Z-form-prone nucleic acids (Z-NAs), it has also been shown that the Z domain of ADAR1 binds DNA G-Quadruplexes (GQ). However, no binding partner of the structurally homologous Z{beta} domain of ADAR1 has been identified to date. Based on AlphaFold and molecular dynamics simulations, it has recently been suggested that the Z{beta} domain of ADAR1 targets its substrate by recognizing GQs. Here, we provide the first experimental evidence for Z{beta} domain binding to select G-quadruplex RNA and DNA in vitro, with structural specificity and low micromolar affinity. We also demonstrate that the Z domains of ZBP1 bind to both DNA and RNA GQs with similar affinity. These findings extend the range of potential functional roles for these proteins and open new hypotheses for testing in cells.
- assay: DNA methylation
- assay: proteomics
- research focus: cell type annotation
- research focus: protein folding & dynamics
- research focus: cell signaling & trafficking
- research focus: chromatin & epigenetic regulation
- approach: experimental assay
- Citations
- 2
- FWCI
- 4.10
- Field percentile
- top 6%
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