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海洋来源的硫酸化聚糖抑制肝素与 . 的黏附蛋白的相互作用。

Marine-Derived Sulfated Glycans Inhibit the Interaction of Heparin with Adhesion Proteins of .

机构信息

The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, College of Life Sciences, Nankai University, Tianjin 300071, China.

Department of Chemistry and Chemical Biology, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.

出版信息

Mar Drugs. 2024 May 20;22(5):232. doi: 10.3390/md22050232.

Abstract

, a notable pathogen behind respiratory infections, employs specialized proteins to adhere to the respiratory epithelium, an essential process for initiating infection. The role of glycosaminoglycans, especially heparan sulfate, is critical in facilitating pathogen-host interactions, presenting a strategic target for therapeutic intervention. In this study, we assembled a glycan library comprising heparin, its oligosaccharide derivatives, and a variety of marine-derived sulfated glycans to screen the potential inhibitors for the pathogen-host interactions. By using Surface Plasmon Resonance spectroscopy, we evaluated the library's efficacy in inhibiting the interaction between adhesion proteins and heparin. Our findings offer a promising avenue for developing novel therapeutic strategies against infections.

摘要

肺炎支原体是引发呼吸道感染的重要病原体之一,它利用特殊的蛋白质黏附在呼吸道上皮细胞上,这是引发感染的关键步骤。糖胺聚糖,特别是肝素硫酸酯,在促进病原体与宿主相互作用方面发挥着关键作用,成为治疗干预的一个重要靶点。在这项研究中,我们构建了一个聚糖文库,其中包含肝素、其低聚糖衍生物和各种海洋来源的硫酸化聚糖,用于筛选可能抑制病原体与宿主相互作用的抑制剂。通过使用表面等离子体共振光谱技术,我们评估了文库抑制黏附蛋白与肝素相互作用的效果。我们的研究结果为开发针对肺炎支原体感染的新型治疗策略提供了一个有前途的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a63/11123223/a3a5de4e340e/marinedrugs-22-00232-g001.jpg

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