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利用杆状病毒MHC/肽展示文库来鉴定T细胞受体配体。

Use of baculovirus MHC/peptide display libraries to characterize T-cell receptor ligands.

作者信息

Crawford Frances, Jordan Kimberly R, Stadinski Brian, Wang Yibing, Huseby Eric, Marrack Philippa, Slansky Jill E, Kappler John W

机构信息

Integrated Department of Immunology, National Jewish Medical and Research Center, Denver, CO 80206, USA.

出版信息

Immunol Rev. 2006 Apr;210:156-70. doi: 10.1111/j.0105-2896.2006.00365.x.

Abstract

Peptide/protein display libraries are powerful tools for identifying and manipulating receptor/ligand pairs. While the large size of bacterial phage display libraries has made them the platform of choice in many applications, often considerable engineering has been required to achieve display of properly folded and active eukaryotic proteins, such as antibodies. This problem has been partially solved in several eukaryotic display systems, e.g. using yeast or retroviruses, but these systems have their own limitations. Recently, baculovirus has been developed as a display system using the virus itself or infected insect cells as the display platform. Here, we review the development and use of baculovirus-infected cells as a platform for display libraries of peptides bound to major histocompatibility complex (MHC) class I (MHCI) or class II (MHCII). We have used fluorescent multimeric soluble T-cell receptors (TCRs) to screen these libraries and to identify peptide antigen mimotopes. We also present some improvements to this system that allow very large libraries to be constructed and screened. We have used these libraries to examine the role of MHCII-bound peptides in the presentation of the staphylococcal enterotoxin A (SEA) and to manipulate an MHCI tumor-associated antigen.

摘要

肽/蛋白质展示文库是识别和操纵受体/配体对的强大工具。虽然细菌噬菌体展示文库规模庞大,使其成为许多应用中的首选平台,但通常需要进行大量工程操作才能实现正确折叠且具有活性的真核蛋白质(如抗体)的展示。在几种真核展示系统中,例如使用酵母或逆转录病毒,这个问题已得到部分解决,但这些系统有其自身的局限性。最近,杆状病毒已被开发为一种展示系统,使用病毒本身或受感染的昆虫细胞作为展示平台。在此,我们综述了杆状病毒感染细胞作为与主要组织相容性复合体(MHC)I类(MHCI)或II类(MHCII)结合的肽展示文库平台的开发和应用。我们已使用荧光多聚体可溶性T细胞受体(TCR)来筛选这些文库并鉴定肽抗原模拟表位。我们还介绍了对该系统的一些改进,这些改进使得能够构建和筛选非常大的文库。我们已使用这些文库来研究与MHCII结合的肽在葡萄球菌肠毒素A(SEA)呈递中的作用,并操纵一种MHCI肿瘤相关抗原。

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