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重组抗体与体外筛选技术。

Recombinant antibodies and in vitro selection technologies.

作者信息

Geyer C Ronald, McCafferty John, Dübel Stefan, Bradbury Andrew R M, Sidhu Sachdev S

机构信息

University of Saskatchewan, Saskatoon, SK, Canada.

出版信息

Methods Mol Biol. 2012;901:11-32. doi: 10.1007/978-1-61779-931-0_2.

Abstract

Over the past decade, the accumulation of detailed knowledge of antibody structure and function has enabled antibody phage display to emerge as a powerful in vitro alternative to hybridoma methods for creating antibodies. Many antibodies produced using phage display technology have unique properties that are not obtainable using traditional hybridoma technologies. In phage display, selections are performed under controlled, in vitro conditions that are tailored to suit demands of the antigen and the sequence encoding the antibody is immediately available. These features obviate many of the limitations of hybridoma methodology, and because the entire process relies on scalable molecular biology techniques, phage display is also suitable for high-throughput applications. Thus, antibody phage display technology is well suited for genome-scale biotechnology and therapeutic applications. This review describes the antibody phage display technology and highlights examples of antibodies with unique properties that cannot easily be obtained by other technologies.

摘要

在过去十年中,对抗体结构和功能的详细了解不断积累,使得抗体噬菌体展示技术成为一种强大的体外方法,可替代杂交瘤技术来制备抗体。许多利用噬菌体展示技术产生的抗体具有独特的性质,这些性质是使用传统杂交瘤技术无法获得的。在噬菌体展示中,筛选是在可控的体外条件下进行的,这些条件经过调整以适应抗原的需求,并且编码抗体的序列可立即获得。这些特性消除了杂交瘤方法的许多局限性,而且由于整个过程依赖于可扩展的分子生物学技术,噬菌体展示也适用于高通量应用。因此,抗体噬菌体展示技术非常适合基因组规模的生物技术和治疗应用。本综述描述了抗体噬菌体展示技术,并重点介绍了具有独特性质、难以通过其他技术轻易获得的抗体实例。

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