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对毒性进行特征分析以及 PirAB - 样蛋白结构的研究,这些蛋白在结构上几乎与引起虾 AHPND 的 PirAB 毒素相同。

Characterization of toxicity and structure of PirAB -like proteins that are structurally almost identical to shrimp AHPND-causing PirAB toxin.

机构信息

College of Food Science and Technology, Shanghai Ocean University, Shanghai, China.

Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.

出版信息

J Fish Dis. 2022 Feb;45(2):315-326. doi: 10.1111/jfd.13557. Epub 2021 Nov 21.

Abstract

PirAB is a binary toxic protein that causes acute hepatopancreatic necrosis disease (AHPND) in shrimp. Their closest homologs, PirA -like and PirB -like proteins, are encoded by two adjacent genes on a non-pVH plasmid from a Vibrio campbellii strain. Herein, PirAB -like protein caused neither abnormalities nor death in shrimp postlarvae (Litopenaeus vannamei); furthermore, typical AHPND clinical signs were not observed. PirA -like protein corresponds to Cry toxin domain III (ligand-binding domain) and likely binds to N-acetylgalactosamine. The C-terminal and N-terminal of PirB -like resemble Cry toxin domain II (receptor-binding domain) and domain I (pore-forming domain), respectively. PirA -like and PirB -like proteins are structurally similar to PirA and PirB, respectively. Subtle structural differences between PirA -like protein and PirA appear to be involved in ligand-binding and binary protein complex formation. The difference in virulence of PirAB -like and PirAB may result from the specific binding of the protein complex to distinct host receptors. These results shed light on the potential functions and host receptors of PirAB -like proteins and their relationship with PirAB.

摘要

PirAB 是一种二元毒性蛋白,可引起虾类急性肝胰腺坏死病(AHPND)。它们最接近的同源物 PirA-样和 PirB-样蛋白,由来自副溶血弧菌菌株的非 pVH 质粒上的两个相邻基因编码。在此,PirAB-样蛋白既未引起虾幼体(凡纳滨对虾)出现异常,也未导致其死亡;此外,未观察到典型的 AHPND 临床症状。PirA-样蛋白对应于 Cry 毒素结构域 III(配体结合域),可能与 N-乙酰半乳糖胺结合。PirB-样蛋白的 C 端和 N 端分别类似于 Cry 毒素结构域 II(受体结合域)和结构域 I(孔形成域)。PirA-样和 PirB-样蛋白在结构上分别类似于 PirA 和 PirB。PirA-样蛋白与 PirA 之间的细微结构差异可能涉及配体结合和二元蛋白复合物的形成。PirAB-样和 PirAB 毒力的差异可能源于蛋白复合物与特定宿主受体的特异性结合。这些结果阐明了 PirAB-样蛋白的潜在功能和宿主受体及其与 PirAB 的关系。

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