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本文引用的文献

1
Coronavirus glycoprotein E1, a new type of viral glycoprotein.冠状病毒糖蛋白E1,一种新型病毒糖蛋白。
J Mol Biol. 1981 Dec 25;153(4):993-1010. doi: 10.1016/0022-2836(81)90463-0.
2
Coronavirus JHM: intracellular protein synthesis.冠状病毒JHM:细胞内蛋白质合成
J Gen Virol. 1981 Mar;53(Pt 1):145-55. doi: 10.1099/0022-1317-53-1-145.
3
Heterologous response of antiserum-treated cell clones from a persistently infected DBT cell line to mouse hepatitis virus.来自持续感染的DBT细胞系的抗血清处理细胞克隆对小鼠肝炎病毒的异源反应。
Jpn J Exp Med. 1982 Dec;52(6):297-302.
4
Monoclonal antibodies to murine hepatitis virus-4 (strain JHM) define the viral glycoprotein responsible for attachment and cell--cell fusion.针对鼠肝炎病毒4型(JHM株)的单克隆抗体确定了负责病毒附着和细胞间融合的病毒糖蛋白。
Virology. 1982 Jun;119(2):358-71. doi: 10.1016/0042-6822(82)90095-2.
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Cell tropism and expression of mouse hepatitis viruses (MHV) in mouse spinal cord cultures.小鼠肝炎病毒(MHV)在小鼠脊髓培养物中的细胞嗜性及表达
Virology. 1982 Jun;119(2):317-31. doi: 10.1016/0042-6822(82)90092-7.
6
Persistent infection with mouse hepatitis virus, JHM strain in DBT cell culture.小鼠肝炎病毒JHM株在DBT细胞培养物中的持续感染
Adv Exp Med Biol. 1981;142:301-8. doi: 10.1007/978-1-4757-0456-3_24.
7
Analysis of the functions of coronavirus glycoproteins by differential inhibition of synthesis with tunicamycin.通过衣霉素对合成的差异抑制分析冠状病毒糖蛋白的功能
Adv Exp Med Biol. 1981;142:133-42. doi: 10.1007/978-1-4757-0456-3_11.
8
Comparison of mouse hepatitis virus strains for pathogenicity in weanling mice infected by various routes.通过不同途径感染断奶小鼠的情况下,小鼠肝炎病毒毒株致病性的比较。
Arch Virol. 1981;70(1):69-73. doi: 10.1007/BF01320795.
9
Viral protein synthesis in mouse hepatitis virus strain A59-infected cells: effect of tunicamycin.小鼠肝炎病毒A59株感染细胞中的病毒蛋白合成:衣霉素的作用
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Genetic variation of neurotropic and non-neurotropic murine coronaviruses.嗜神经和非嗜神经小鼠冠状病毒的基因变异
J Gen Virol. 1981 May;54(Pt 1):67-74. doi: 10.1099/0022-1317-54-1-67.

小鼠肝炎病毒JHM株小噬斑突变体的特性分析

Characterization of small plaque mutants of mouse hepatitis virus, JHM strain.

作者信息

Makino S, Taguchi F, Hayami M, Fujiwara K

出版信息

Microbiol Immunol. 1983;27(5):445-54. doi: 10.1111/j.1348-0421.1983.tb00603.x.

DOI:10.1111/j.1348-0421.1983.tb00603.x
PMID:6312277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7168364/
Abstract

Two small plaque mutants designated as 1a and 2c were isolated from DBT cells persistently infected with the JHM strain of mouse hepatitis virus. Unlike the wild type JHM, these two mutant viruses grew more slowly with no prominent cell fusion. The buoyant densities of the mutants were slightly lower and 2c was revealed to have fewer peplomers than JHM by electron microscopy. The purified JHM contained five polypeptides with molecular weights (M.W.) of 260,000, 105,000 (GP105), 65,000, 60,000 (P60), and 23,000 (GP23). In addition to two polypeptides, P60 and GP23, which were common to JHM and the mutants, 1a was found to contain three other specific polypeptides with M.W. of 180,000 (GP180), 110,000, and 95,000 (GP95), while 2c had GP180, GP105, GP95, and one with a M.W. of 175,000. All of these polypeptides were shown to be glycosylated except for P60. After bromelain treatment, all these viruses lost the peplomers and contained P60 and another new 18,000 dalton polypeptide.

摘要

从持续感染小鼠肝炎病毒JHM株的DBT细胞中分离出两个小斑块突变体,分别命名为1a和2c。与野生型JHM不同,这两种突变病毒生长较慢,没有明显的细胞融合现象。突变体的浮力密度略低,通过电子显微镜观察发现2c的纤突比JHM少。纯化的JHM含有五种分子量分别为260,000、105,000(GP105)、65,000、60,000(P60)和23,000(GP23)的多肽。除了JHM和突变体共有的两种多肽P60和GP23外,发现1a还含有另外三种分子量分别为180,000(GP180)、110,000和95,000(GP95)的特异性多肽,而2c含有GP180、GP105、GP95和一种分子量为175,000的多肽。除P60外,所有这些多肽都被证明是糖基化的。用菠萝蛋白酶处理后,所有这些病毒都失去了纤突,并含有P60和另一种新的18,000道尔顿的多肽。