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1
Coronavirus IBV: partial amino terminal sequencing of spike polypeptide S2 identifies the sequence Arg-Arg-Phe-Arg-Arg at the cleavage site of the spike precursor propolypeptide of IBV strains Beaudette and M41.冠状病毒传染性支气管炎病毒(IBV):刺突多肽S2的部分氨基末端测序确定了IBV毒株Beaudette和M41的刺突前体多肽裂解位点处的序列为精氨酸-精氨酸-苯丙氨酸-精氨酸-精氨酸。
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2
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Coronavirus IBV: removal of spike glycopolypeptide S1 by urea abolishes infectivity and haemagglutination but not attachment to cells.冠状病毒传染性支气管炎病毒(IBV):用尿素去除刺突糖多肽S1可消除其感染性和血凝作用,但不会消除其对细胞的附着。
J Gen Virol. 1986 Jul;67 ( Pt 7):1443-8. doi: 10.1099/0022-1317-67-7-1443.
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Virus Res. 1986 Aug;5(2-3):253-63. doi: 10.1016/0168-1702(86)90022-5.

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Cloning and DNA sequence of double-stranded copies of haemagglutinin genes from H2 and H3 strains elucidates antigenic shift and drift in human influenza virus.H2和H3毒株血凝素基因双链拷贝的克隆及DNA序列分析阐明了人流感病毒的抗原转变和抗原漂移。
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冠状病毒传染性支气管炎病毒(IBV):刺突多肽S2的部分氨基末端测序确定了IBV毒株Beaudette和M41的刺突前体多肽裂解位点处的序列为精氨酸-精氨酸-苯丙氨酸-精氨酸-精氨酸。

Coronavirus IBV: partial amino terminal sequencing of spike polypeptide S2 identifies the sequence Arg-Arg-Phe-Arg-Arg at the cleavage site of the spike precursor propolypeptide of IBV strains Beaudette and M41.

作者信息

Cavanagh D, Davis P J, Pappin D J, Binns M M, Boursnell M E, Brown T D

出版信息

Virus Res. 1986 Feb;4(2):133-43. doi: 10.1016/0168-1702(86)90037-7.

DOI:10.1016/0168-1702(86)90037-7
PMID:3010595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7133853/
Abstract

The spike protein of avian infectious bronchitis coronavirus comprises two glycopolypeptides S1 and S2 derived by cleavage of a proglycopolypeptide So, the nucleotide sequence of which has recently been determined for the Beaudette strain (Binns, M.M. et al., 1985, J. Gen. Virol. 66, 719-726). The order of the two glycopolypeptides within So is aminoterminus(N)-S1-S2-carboxyterminus(C). To locate the N-terminus of S2 we have performed partial amino acid sequencing on S2 from IBV-Beaudette labelled with [3H]serine and from the related strain labelled with [3H]valine, leucine and isoleucine. The residues identified and their positions relative to the N-terminus of S2 were: serine, 13; valine, 6, 12; leucine, none in the first 20 residues; isoleucine, 2, 19. These results identified the N-terminus of S2 of IBV-Beaudette as serine, 520 residues from the N-terminus of S1, excluding the signal sequence. Immediately to the N-terminal side of residue 520 So has the sequence Arg-Arg-Phe-Arg-Arg; similar basic connecting peptides are a feature of several other virus spike glycoproteins. It was deduced that for IBV-Beaudette S1 comprises 519 residues (Mr 57.0K) or 514 residues (56.2K) if the connecting peptide was to be removed by carboxypeptidase-like activity in vivo while S2 has 625 residues (69.2K). Nucleotide sequencing of the cleavage region of the So gene of IBV-M41 revealed the same connecting peptide as IBV-Beaudette and that the first 20 N-terminal residues of S2 of IBV-M41 were identical to those of the Beaudette strain. IBV-Beaudette grown in Vero cells had some uncleaved So; this was cleavable by 10 micrograms/ml of trypsin and of chymotrypsin. Partial N-terminal analysis of S1 from IBV-M41 identified leucine and valine residues at positions 2 and 9 respectively from the N-terminus. This confirms the identification, made by Binns et al. (1985), of the N-terminus of S1 and the end of the signal sequence of the IBV-Beaudette spike propolypeptide. N-terminal sequencing of [3H]leucine-labelled IBV-Beaudette membrane (M) polypeptide showed leucine residues at positions 8, 16 and 22 from the N-terminus; these results confirm the open reading frame identified by M.E.G. Boursnell et al. (1984, Virus Res. 1, 303-313) in the nucleotide sequence of M. The N-terminus of the nucleocapsid (N) polypeptide appeared to be blocked.

摘要

禽传染性支气管炎冠状病毒的刺突蛋白由前体糖多肽So裂解产生的两种糖多肽S1和S2组成,最近已确定了Beaudette株So的核苷酸序列(Binns, M.M.等人,1985年,《普通病毒学杂志》66卷,719 - 726页)。So中两种糖多肽的顺序为氨基端(N)-S1-S2-羧基端(C)。为了确定S2的N端,我们对用[3H]丝氨酸标记的IBV-Beaudette的S2以及用[3H]缬氨酸、亮氨酸和异亮氨酸标记的相关毒株的S2进行了部分氨基酸测序。鉴定出的残基及其相对于S2 N端的位置为:丝氨酸,第13位;缬氨酸,第6、12位;亮氨酸,前20个残基中无;异亮氨酸,第2、19位。这些结果确定IBV-Beaudette的S2的N端为丝氨酸,位于S1 N端下游520个残基处,不包括信号序列。在残基520的紧邻N端一侧,So的序列为Arg-Arg-Phe-Arg-Arg;类似的碱性连接肽是其他几种病毒刺突糖蛋白的一个特征。据推测,对于IBV-Beaudette,S1包含519个残基(Mr 57.0K),如果连接肽在体内被类似羧肽酶的活性去除,则包含514个残基(56.2K),而S2有625个残基(69.2K)。IBV-M41的So基因裂解区的核苷酸测序显示其连接肽与IBV-Beaudette相同,且IBV-M41的S2的前20个N端残基与Beaudette株相同。在Vero细胞中生长的IBV-Beaudette有一些未裂解的So;它可被10微克/毫升的胰蛋白酶和胰凝乳蛋白酶裂解。对IBV-M41的S1进行的部分N端分析确定,分别在N端第2和第9位有亮氨酸和缬氨酸残基。这证实了Binns等人(1985年)对IBV-Beaudette刺突前体多肽的S1的N端和信号序列末端的鉴定。对用[3H]亮氨酸标记的IBV-Beaudette膜(M)多肽进行的N端测序显示,在N端第8、16和22位有亮氨酸残基;这些结果证实了M.E.G. Boursnell等人(1984年,《病毒研究》1卷,303 - 313页)在M的核苷酸序列中确定的开放阅读框。核衣壳(N)多肽的N端似乎被封闭。