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预测病毒-宿主相互作用和鉴定 DENV-2 与 SH3 结构域相互作用的热点残基。

Prediction of virus-host interactions and identification of hot spot residues of DENV-2 and SH3 domain interactions.

机构信息

Department of Bioinformatics and Biotechnology, Asian University for Women, Chattogram, Bangladesh.

Centre for Inflammation, Centenary Institute and the University of Technology Sydney, School of Life Sciences, Faculty of Science, Sydney, NSW, Australia.

出版信息

Arch Microbiol. 2024 Mar 14;206(4):162. doi: 10.1007/s00203-024-03892-x.

Abstract

Dengue virus, particularly serotype 2 (DENV-2), poses a significant global health threat, and understanding the molecular basis of its interactions with host cell proteins is imperative for developing targeted therapeutic strategies. This study elucidated the interactions between proline-enriched motifs and Src homology 3 (SH3) domain. The SH3 domain is pivotal in mediating protein-protein interactions, particularly by recognizing and binding to proline-rich regions in partner proteins. Through a computational pipeline, we analyzed the interactions and binding modes of proline-enriched motifs with SH3 domains, identified new potential DENV-2 interactions with the SH3 domain, and revealed potential hot spot residues, underscoring their significance in the viral life cycle. This comprehensive analysis provides crucial insights into the molecular basis of DENV-2 infection, highlighting conserved and serotype-specific interactions. The identified hot spot residues offer potential targets for therapeutic intervention, laying the foundation for developing antiviral strategies against Dengue virus infection. These findings contribute to the broader understanding of viral-host interactions and provide a roadmap for future research on Dengue virus pathogenesis and treatment.

摘要

登革热病毒,特别是血清型 2(DENV-2),对全球健康构成重大威胁,了解其与宿主细胞蛋白相互作用的分子基础对于开发靶向治疗策略至关重要。本研究阐明了富含脯氨酸基序与Src 同源 3(SH3)结构域之间的相互作用。SH3 结构域在介导蛋白质-蛋白质相互作用中起着关键作用,特别是通过识别和结合伴侣蛋白中的脯氨酸丰富区域。通过计算分析,我们分析了富含脯氨酸基序与 SH3 结构域的相互作用和结合模式,确定了新的潜在 DENV-2 与 SH3 结构域的相互作用,并揭示了潜在的热点残基,强调了它们在病毒生命周期中的重要性。这项全面的分析为 DENV-2 感染的分子基础提供了重要的见解,突出了保守和血清型特异性的相互作用。鉴定的热点残基为治疗干预提供了潜在的靶点,为开发针对登革热病毒感染的抗病毒策略奠定了基础。这些发现有助于更全面地了解病毒-宿主相互作用,并为登革热病毒发病机制和治疗的未来研究提供了路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c522/10940428/b414f38f8013/203_2024_3892_Fig1_HTML.jpg

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