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Epitope mapping and functional analysis of sigma A and sigma NS proteins of avian reovirus

机译:禽呼肠孤病毒sigma a和sigma Ns蛋白的表位作图和功能分析

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摘要

We have previously shown that avian reovirus (ARV) sigmaA and sigmaNS proteins possess dsRNA and ssRNA binding activity and suggested that there are two epitopes on sigmaA (I and II) and three epitopes (A, B, and C) on sigmaNS. To further define the location of epitopes on sigmaA and sigmaNS proteins and to further elucidate the biological functions of these epitopes by using monoclonal antibodies (MAbs) 62, 1F9, H1E1, and 4A 123 against the ARV S1133 strain, the full-length and deletion fragments of S2 and S4 genes of ARV generated by polymerase chain reaction (PCR) were cloned into pET32 expression vectors and the fusion proteins were overexpressed in Escherichia coli BL21 strain. Epitope mapping using MAbs and E. coli-expressed deletion fragments of sigmaA and sigmaNS of the ARV S1133 strain, synthetic peptides, and the cross reactivity of MAbs to heterologous ARV strains demonstrated that epitope II on sigmaA was located at amino acid residues (340)QWVMAGLVSAA(350) and epitope B on sigmaNS at amino acid residues (180)MLDMVDGRP(188). The MAbs (62, 1F9, and H1E1) directed against epitopes 11 and B did not require the native conformation of sigmaA and sigmaNS, suggesting that their binding activities were conformation-independent. On the other hand, MAb 4A123 only reacted with complete sigmaNS but not with truncated o-NS fusion proteins in Western blot, suggesting that the binding activity of MAb to epitope A on o-NS was conformation-dependent. Amino acid sequence analysis and the binding assays of MAb 62 to heterologous ARV strains suggested that epitope 11 on sigmaA was highly conserved among ARV strains and that this epitope is suitable as a serological marker for the detection of ARV antibodies following natural infection in chickens. On the contrary, an amino acid substitution at position 183 (M to V) in epitope B of ARV could hinder the reactivity of the sigmaNS with MAb 1F9. The sigmaNS of ARV with ssRNA-binding activity could be blocked by monoclonal antibody 1F9. The epitope B on (sigmaNS is required for ssRNA binding because its deletion fully abolished the ssRNA binding activity of sigmaNS. (C) 2004 Elsevier Inc. All rights reserved.
机译:先前我们已经证明禽呼肠孤病毒(ARV)sigmaA和sigmaNS蛋白具有dsRNA和ssRNA结合活性,并建议在sigmaA上存在两个表位(I和II),在sigmaNS上存在三个表位(A,B和C)。为了进一步定义表位在sigmaA和sigmaNS蛋白上的位置并通过使用抗ARV S1133菌株的单克隆抗体(MAb)62、1F9,H1E1和4A 123进一步阐明这些表位的生物学功能,全长和缺失将通过聚合酶链反应(PCR)产生的ARV的S2和S4基因的片段克隆到pET32表达载体中,并且融合蛋白在大肠杆菌BL21菌株中过表达。使用MAb和ARV S1133菌株sigmaA和sigmaNS的大肠杆菌表达缺失片段进行表位作图,合成肽以及MAb与异源ARV菌株的交叉反应性表明sigmaA上的表位II位于氨基酸残基(340) QWVMAGLVSAA(350)和sigmaNS上的氨基酸残基上的表位B(180)MLDMVDGRP(188)。针对表位11和B的MAb(62、1F9和H1E1)不需要sigmaA和sigmaNS的天然构象,表明它们的结合活性不依赖于构象。另一方面,MAb 4A123仅与完整的sigmaNS反应,而与截短的o-NS融合蛋白不反应,这表明MAb与o-NS上表位A的结合活性是构象依赖性的。氨基酸序列分析和MAb 62与异源ARV株的结合测定表明,sigmaA上的表位11在ARV株之间是高度保守的,并且该表位适合作为血清学标记物,用于检测鸡自然感染后的ARV抗体。相反,ARV表位B中第183位(M到V)的氨基酸取代可能会阻碍sigmaNS与MAb 1F9的反应性。具有ssRNA结合活性的ARV的sigmaNS可以被单克隆抗体1F9阻断。 ssRNA结合需要表位B(sigmaNS是ssRNA结合所必需的,因为其缺失完全消除了sigmaNS的ssRNA结合活性。(C)2004 Elsevier Inc.保留所有权利。

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