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通过分子对接鉴定出的靶向白血病细胞中翻译控制肿瘤蛋白的肽适配体。

Peptide aptamer identified by molecular docking targeting translationally controlled tumor protein in leukemia cells.

作者信息

Kadioglu Onat, Efferth Thomas

机构信息

Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, University of Mainz, Staudinger Weg 5, 55128, Mainz, Germany.

出版信息

Invest New Drugs. 2016 Aug;34(4):515-21. doi: 10.1007/s10637-016-0339-6. Epub 2016 Mar 14.

Abstract

Bioinformatics screening and molecular docking analyses were utilized to select high affinity peptides targeting translationally controlled tumor protein (TCTP). Selected peptide aptamers were tested towards cancer cell lines with different levels of TCTP expression. One peptide (WGQWPYHC) revealed specific cytotoxicity according to the TCTP expression in tumor cells without affecting normal cells. Western blot analysis showed peptide-induced down-regulation of TCTP as primary target as well as of cell-cycle related downstream proteins (CDK2, CDK6, Cyclin D3) in MOLT-4 leukemia cells. "WGQWPYHC" deserves further analysis for targeted therapy of TCTP-expressing tumor cells. Graphical abstract Molecular docking on TCTP, cytotoxicity toward MOLT-4 leukemia cell line and downregulation of CDK2, CDK6, CyclinD3 and TCTP proteins.

摘要

利用生物信息学筛选和分子对接分析来选择靶向翻译控制肿瘤蛋白(TCTP)的高亲和力肽段。针对具有不同TCTP表达水平的癌细胞系对所选的肽适配体进行测试。一种肽(WGQWPYHC)根据肿瘤细胞中TCTP的表达显示出特异性细胞毒性,而不影响正常细胞。蛋白质印迹分析表明,在MOLT-4白血病细胞中,该肽诱导TCTP作为主要靶点以及细胞周期相关下游蛋白(CDK2、CDK6、细胞周期蛋白D3)的下调。“WGQWPYHC”对于表达TCTP的肿瘤细胞的靶向治疗值得进一步分析。图形摘要:TCTP的分子对接、对MOLT-4白血病细胞系的细胞毒性以及CDK2、CDK6、细胞周期蛋白D3和TCTP蛋白的下调。

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