Hightower L E, Morrison T G, Bratt M A
J Virol. 1975 Dec;16(6):1599-607. doi: 10.1128/JVI.16.6.1599-1607.1975.
We have studied the relationships among the polypeptides of Newcastle disease virus by using both kinetic and tryptic peptide analyses. The results of our tryptic peptide analyses suggest that there are at least six unique viral polypeptides--L, HN, FO(F), NP, M, and a 47,000-dalton polypeptide. The small virion glycopolypeptide F is related to FO, a glycopolypeptide found only in infected cells. In addition, several smaller polypeptides, including a 53,000-dalton polypeptide found both in purified virions and in infected cells, are related to the nucleocaspid protein. Kinetic analysis of each viral polypeptide reveals that all of the major viral polypeptides, with the possible exception of L, are stable after an amino acid chase. A precursor-product relationship between FO and F was not demonstrable by pulse-chase experiments. Also, almost the same relative amount of F, the putative product, was present in infected cultures after either 5 or 30 min of radioisotopic labeling. These results suggest that FO is processed rapidly.
我们通过动力学分析和胰蛋白酶肽分析研究了新城疫病毒多肽之间的关系。胰蛋白酶肽分析结果表明,至少存在六种独特的病毒多肽——L、HN、FO(F)、NP、M以及一种47,000道尔顿的多肽。小病毒粒子糖多肽F与仅在感染细胞中发现的糖多肽FO相关。此外,几种较小的多肽,包括在纯化病毒粒子和感染细胞中均发现的一种53,000道尔顿的多肽,与核衣壳蛋白相关。对每种病毒多肽的动力学分析表明,除L可能外,所有主要病毒多肽在氨基酸追踪后都是稳定的。脉冲追踪实验未证明FO和F之间存在前体-产物关系。而且,在放射性同位素标记5分钟或30分钟后,感染培养物中假定产物F的相对含量几乎相同。这些结果表明FO加工迅速。