Suppr超能文献

工程改造M13噬菌体以在pVIII上展示HER2模拟表位用于疫苗开发。

Engineering M13 bacteriophage to display HER2 mimotopes on pVIII for vaccine development.

作者信息

Nazeri Narmin, Bahrami Yadollah, Barzegari Ebrahim, Mohammadi Mohammad, Kazemi-Lomedasht Fatemeh, Rajabibazl Masoumeh, Mohammadzadeh Sara

机构信息

Department of Medical Biotechnology, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Sci Rep. 2025 Jul 1;15(1):22285. doi: 10.1038/s41598-025-08032-z.

Abstract

HER2-positive breast cancer is a subtype characterized by overexpression of the human epidermal growth factor receptor 2 (HER2), which is associated with aggressive tumor growth and poor prognosis. Peptide mimics of HER2 epitopes, recognized by tumor growth-inhibitory antibodies like trastuzumab, have the potential to be developed into effective vaccines. Active immunization with these mimotopes could induce tumor-inhibitory antibodies, offering a cost-effective alternative to trastuzumab therapy. This study aimed to design high-affinity mimotopes to trastuzumab using bioinformatics tools and to evaluate the potential of M13 bacteriophages as platforms for displaying these mimotopes. Using the Peptiderive server, peptide sequences involved in binding HER2 to trastuzumab were identified and refined. Docking studies validated their enhanced binding affinity to trastuzumab. The optimized mimotopes were then displayed on the pVIII coat protein of M13 bacteriophages using the PAK8 phagemid vector. ELISA assays confirmed the binding of these recombinant phages to trastuzumab.This study highlights the effectiveness of using bioinformatics tools to enhance mimotope design for therapeutic applications. The M13 bacteriophage displaying optimized mimotopes shows potential as a vaccine candidate for HER2-positive breast cancer, offering a promising approach to overcoming current limitations of trastuzumab therapy.

摘要

人表皮生长因子受体2(HER2)阳性乳腺癌是一种以HER2过表达为特征的亚型,这与肿瘤的侵袭性生长和不良预后相关。被曲妥珠单抗等肿瘤生长抑制抗体识别的HER2表位肽模拟物有潜力被开发成有效的疫苗。用这些模拟表位进行主动免疫可诱导肿瘤抑制抗体,为曲妥珠单抗治疗提供一种经济有效的替代方案。本研究旨在利用生物信息学工具设计与曲妥珠单抗具有高亲和力的模拟表位,并评估M13噬菌体作为展示这些模拟表位平台的潜力。使用Peptiderive服务器,鉴定并优化了参与HER2与曲妥珠单抗结合的肽序列。对接研究验证了它们与曲妥珠单抗增强的结合亲和力。然后使用PAK8噬菌粒载体将优化后的模拟表位展示在M13噬菌体的pVIII外壳蛋白上。酶联免疫吸附测定(ELISA)证实了这些重组噬菌体与曲妥珠单抗的结合。本研究突出了使用生物信息学工具增强模拟表位设计用于治疗应用的有效性。展示优化模拟表位的M13噬菌体显示出作为HER2阳性乳腺癌候选疫苗的潜力,为克服曲妥珠单抗治疗目前的局限性提供了一种有前景的方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验