Mattion N M, Harnish E C, Crowley J C, Reilly P A
Wyeth-Lederle Vaccines and Pediatrics, Viral Vaccine Research, Pearl River, New York 10965, USA.
J Virol. 1996 Nov;70(11):8124-7. doi: 10.1128/JVI.70.11.8124-8127.1996.
Poliovirus vectors are being studied as potential vaccine delivery systems, with foreign genetic sequences incorporated as part of the viral genome. The foreign sequences are expressed as part of the viral polyprotein. Addition of proteolytic cleavage sites at the junction of the foreign polypeptide and the viral proteins results in cleavage during polyprotein processing. The ability of foot-and-mouth disease virus (FMDV) 2A to mediate proteolytic cleavage in the context of poliovirus vectors was studied. The results demonstrate that FMDV 2A is able to generate cleavage of the foreign antigen from the viral polyprotein. A second cleavage event between the FMDV 2A peptide and the foreign protein was also observed.
脊髓灰质炎病毒载体正作为潜在的疫苗递送系统进行研究,其中外源基因序列作为病毒基因组的一部分被整合。外源序列作为病毒多聚蛋白的一部分被表达。在外源多肽与病毒蛋白的连接处添加蛋白水解切割位点可导致多聚蛋白加工过程中的切割。研究了口蹄疫病毒(FMDV)2A在脊髓灰质炎病毒载体背景下介导蛋白水解切割的能力。结果表明,FMDV 2A能够从病毒多聚蛋白中切割出外源抗原。还观察到FMDV 2A肽与外源蛋白之间的第二次切割事件。