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扩展KHSRP蛋白的功能:对DNA G-四链体结合的见解

Expanding the Functions of KHSRP Protein: Insights into DNA G-Quadruplex Binding.

作者信息

Russomanno Pasquale, Zizza Pasquale, Cerofolini Linda, D'Aria Federica, Iachettini Sara, Di Vito Serena, Biroccio Annamaria, Amato Jussara, Fragai Marco, Pagano Bruno

机构信息

Department of Pharmacy, University of Naples Federico II, Naples, 80131, Italy.

CERM-CIRMMP and Department of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino (FI), 50019, Italy.

出版信息

Adv Sci (Weinh). 2025 Feb;12(8):e2410086. doi: 10.1002/advs.202410086. Epub 2025 Jan 6.

Abstract

KHSRP (KH-type splicing regulatory protein) is a multifunctional nucleic acid-binding protein that regulates various cellular processes, with critical roles in controlling gene expression. G-quadruplexes (G4s) are noncanonical nucleic acid structures involved in essential cellular activities, including gene expression, and are recognized as potential therapeutic targets in cancer. The biological functions of G4s are mediated by proteins making their formation highly dynamic within cells. Therefore, the recognition of G4s by specific proteins is crucial for modulating physiological and pathological pathways. Given the growing interest in DNA G4s, a deeper understanding of the proteins that interact with them and their molecular recognition is imperative. This study demonstrates that KHSRP binds to these DNA structures. Biophysical analyses provide insights into the thermodynamics, kinetics, and structural aspects of these interactions, showing that G4 structural variability significantly influences KHSRP binding, in which the KH3 protein domain plays a key role. Validation of these interactions in cancer cells further highlights their biological relevance. Notably, the G4 ligand pyridostatin affects KHSRP/G4 interactions both in vitro and in cells, suggesting that small molecules can modulate this molecular recognition. These findings underscore KHSRP's potential role in regulating cellular mechanisms through binding to G4-forming DNA, positioning it as a possible therapeutic target in cancer.

摘要

KH型剪接调节蛋白(KHSRP)是一种多功能核酸结合蛋白,可调节多种细胞过程,在控制基因表达中起关键作用。G-四链体(G4s)是参与包括基因表达在内的基本细胞活动的非规范核酸结构,被认为是癌症潜在的治疗靶点。G4s的生物学功能由蛋白质介导,使其在细胞内的形成高度动态化。因此,特定蛋白质对G4s的识别对于调节生理和病理途径至关重要。鉴于对DNA G4s的兴趣日益浓厚,深入了解与它们相互作用的蛋白质及其分子识别势在必行。本研究表明KHSRP与这些DNA结构结合。生物物理分析为这些相互作用的热力学、动力学和结构方面提供了见解,表明G4结构变异性显著影响KHSRP结合,其中KH3蛋白结构域起关键作用。在癌细胞中对这些相互作用的验证进一步突出了它们的生物学相关性。值得注意的是,G4配体吡啶抑素在体外和细胞内均影响KHSRP/G4相互作用,表明小分子可调节这种分子识别。这些发现强调了KHSRP通过与形成G4的DNA结合在调节细胞机制中的潜在作用,将其定位为癌症可能的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009b/11848572/27d5ed12fb28/ADVS-12-2410086-g003.jpg

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