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噬菌体-DMS:一种用于精细定位抗体表位的综合方法。

Phage-DMS: A Comprehensive Method for Fine Mapping of Antibody Epitopes.

作者信息

Garrett Meghan E, Itell Hannah L, Crawford Katharine H D, Basom Ryan, Bloom Jesse D, Overbaugh Julie

机构信息

Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

Molecular and Cellular Biology Graduate Program, University of Washington and Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

iScience. 2020 Sep 29;23(10):101622. doi: 10.1016/j.isci.2020.101622. eCollection 2020 Oct 23.

Abstract

Understanding the antibody response is critical to developing vaccine and antibody-based therapies and has inspired the recent development of new methods to isolate antibodies. Methods to define the antibody-antigen interactions that determine specificity or allow escape have not kept pace. We developed Phage-DMS, a method that combines two powerful approaches-immunoprecipitation of phage peptide libraries and deep mutational scanning (DMS)-to enable high-throughput fine mapping of antibody epitopes. As an example, we designed sequences encoding all possible amino acid variants of HIV Envelope to create phage libraries. Using Phage-DMS, we identified sites of escape predicted using other approaches for four well-characterized HIV monoclonal antibodies with known linear epitopes. In some cases, the results of Phage-DMS refined the epitope beyond what was determined in previous studies. This method has the potential to rapidly and comprehensively screen many antibodies in a single experiment to define sites essential for binding interactions.

摘要

了解抗体反应对于开发疫苗和基于抗体的疗法至关重要,并推动了近期分离抗体新方法的发展。然而,用于确定决定特异性或导致逃逸的抗体-抗原相互作用的方法却未能跟上步伐。我们开发了噬菌体深度突变扫描(Phage-DMS)方法,该方法结合了两种强大的方法——噬菌体肽库免疫沉淀和深度突变扫描(DMS),以实现抗体表位的高通量精细定位。例如,我们设计了编码HIV包膜所有可能氨基酸变体的序列来创建噬菌体库。使用Phage-DMS,我们确定了使用其他方法预测的四个具有已知线性表位的特征明确的HIV单克隆抗体的逃逸位点。在某些情况下,Phage-DMS的结果对表位的细化超出了先前研究的确定范围。这种方法有可能在单个实验中快速、全面地筛选许多抗体,以确定结合相互作用所必需的位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aacf/7566095/32cbfc4facd3/fx1.jpg

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