Srivastava A K, Morita K, Igarashi A
Department of Virology, Nagasaki University, Japan.
Acta Virol. 1990 May;34(3):228-38.
Envelope glycoprotein (E) prepared from purified Japanese encephalitis (JE) virus was cleaved with cyanogen bromide (CNBr) followed by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). Mice were immunized with 36 kD, 27 kD, and 8 kD bands from CNBr-cleaved and 54 kD band from control specimens. Neutralization test was positive in one out of two anti-54 kD, in none of the anti-36 kD, and all of anti-27 kD and anti-8 kD sera at 1:10 dilution. Geometrical mean ELISA titre was the highest for anti-54 kD followed by anti-36 kD, anti-27 kD, and anti-8 kD sera. Reactivity of these sera to CNBr-cleaved fragments in Western blotting indicated that the 8 kD fragment was a part of the 27 kD but was not included in the 36 kD fragment, while the 27 kD and 36 kD fragments shared an overlapping part. These fragments were located on the E protein by N-terminal amino acid sequencing of each fragment purified by reversed-phase high-performance liquid chromatography and by comparison with the nucleotide sequence of the E protein gene. The 36 kD fragment was located between the third and the ninth methionine and covered most of the N-terminal side of the E protein. In contrast, the 27 kD fragment was located between the fourth and the tenth methionine and included the 8 kD fragment which was situated between the ninth and the tenth methionine near to the C-terminus of the E protein. Denaturation-resistant neutralizing epitope(s) appeared to be present on the 8 kD fragment, but not on the 36 kD fragment.
从纯化的日本脑炎(JE)病毒中制备包膜糖蛋白(E),用溴化氰(CNBr)裂解,然后进行十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)。用来自CNBr裂解产物的36 kD、27 kD和8 kD条带以及对照标本的54 kD条带免疫小鼠。在1:10稀释度下,两种抗54 kD血清中有一份中和试验呈阳性,抗36 kD血清均为阴性,抗27 kD和抗8 kD血清均为阳性。抗54 kD血清的几何平均ELISA滴度最高,其次是抗36 kD、抗27 kD和抗8 kD血清。这些血清在蛋白质免疫印迹中对CNBr裂解片段的反应性表明,8 kD片段是27 kD片段的一部分,但不包含在36 kD片段中,而27 kD和36 kD片段有重叠部分。通过对经反相高效液相色谱纯化的每个片段进行N端氨基酸测序,并与E蛋白基因的核苷酸序列进行比较,确定这些片段位于E蛋白上。36 kD片段位于第三个和第九个甲硫氨酸之间,覆盖了E蛋白大部分的N端。相反,27 kD片段位于第四个和第十个甲硫氨酸之间,包括位于靠近E蛋白C端的第九个和第十个甲硫氨酸之间的8 kD片段。抗变性中和表位似乎存在于8 kD片段上,而不存在于36 kD片段上。