Cavanagh D
J Gen Virol. 1983 Aug;64 (Pt 8):1787-91. doi: 10.1099/0022-1317-64-8-1787.
The surface projections (peplomers) of avian infectious bronchitis virus (IBV) strain M41 have been separated from the nucleocapsid (N) and matrix (M) proteins by sedimentation in a sucrose gradient after virus disruption by the non-ionic detergent Nonidet P40. The peplomers comprised two glycopolypeptides of mol. wt. 90 X 10(3) (90K; S1) and 84K (S2), shown by analysis of differentially radiolabelled virus to be present in equimolar proportions. Polypeptides of 75K and 110K, which were detected by Coomassie Brilliant Blue staining in similar amounts to S1 and S2 in some unlabelled virus preparations, were absent from peplomer preparations and are probably host cell polypeptides. The S1:S2:N:M polypeptide molar ratio for IBV-M41 was approximately 1:1:6:15.
禽传染性支气管炎病毒(IBV)M41株的表面突起(纤突),在通过非离子去污剂Nonidet P40破坏病毒后,经蔗糖梯度沉降已与核衣壳(N)蛋白和基质(M)蛋白分离。纤突由两种分子量分别为90×10³(90K;S1)和84K(S2)的糖蛋白多肽组成,通过对差异放射性标记病毒的分析表明它们以等摩尔比例存在。在一些未标记病毒制剂中,用考马斯亮蓝染色检测到的75K和110K多肽,其含量与S1和S2相似,但在纤突制剂中不存在,可能是宿主细胞多肽。IBV-M41的S1:S2:N:M多肽摩尔比约为1:1:6:15。