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针对流感跨膜蛋白 M2 胞质域的抗体的选择和验证。

Selection and verification of antibodies against the cytoplasmic domain of M2 of influenza, a transmembrane protein.

机构信息

Biosecurity and Public Health, Bioscience Division, Los Alamos National Laboratory , Los Alamos, NM, USA.

Specifica Inc ., Santa Fe, NM, USA.

出版信息

MAbs. 2020 Jan-Dec;12(1):1843754. doi: 10.1080/19420862.2020.1843754.

Abstract

Interactions between the cytoplasmic domains of viral transmembrane proteins and host machinery often determine the outcome of viral infection. The M2 protein of influenza A has been identified as a key player in autophagy-mediated viral replication. Here, we describe the engineering and validation of an antibody specific for the cytoplasmic domain of the M2 protein. Through phage and yeast display selection techniques, we obtained an antibody that recognizes: 1) the M2 cytoplasmic domain purified from bacterial inclusion bodies and refolded, 2) full-length M2 recombinant protein expressed in mammalian cells, and 3) native M2 protein in influenza A infected cells. This antibody can serve as a molecular tool to enhance our knowledge of protein-protein interactions between influenza A virus and the host cell machinery. We anticipate the methods described herein will further the development of antibodies specific to the cytoplasmic domains of transmembrane proteins.

摘要

病毒跨膜蛋白的细胞质域与宿主机制之间的相互作用通常决定了病毒感染的结果。甲型流感的 M2 蛋白已被确定为自噬介导的病毒复制中的关键因素。在这里,我们描述了针对 M2 蛋白细胞质域的抗体的工程化和验证。通过噬菌体和酵母展示选择技术,我们获得了一种抗体,该抗体可识别:1)从细菌包涵体中纯化并重折叠的 M2 细胞质域,2)在哺乳动物细胞中表达的全长 M2 重组蛋白,以及 3)在感染流感 A 的细胞中的天然 M2 蛋白。该抗体可用作分子工具,以增强我们对甲型流感病毒与宿主细胞机制之间蛋白-蛋白相互作用的认识。我们预计本文所述的方法将进一步开发针对跨膜蛋白细胞质域的特异性抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a05/7678940/adcf28a24e5e/KMAB_A_1843754_F0001_OC.jpg

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