Identification by mass spectroscopy of three major early proteins associated with virosomes in vaccinia virus-infected cells

被引:23
作者
Murcia-Nicolas, A
Bolbach, G
Blais, JC
Beaud, G
机构
[1] Univ Paris 06, Inst Jacques Monod, CNRS, F-75251 Paris 05, France
[2] Univ Nacl Colombia AA, Inst Biotecnol, Bogota 14490, Colombia
[3] Univ Paris 06, Chim Struct Organ & Biol Lab, CNRS, UMR 7613, Paris 6, France
关键词
vaccinia virus; MALDI MS; virosomes; H5R; E3L; E5R;
D O I
10.1016/S0168-1702(98)00114-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Virosomes are cytoplasmic sites of replication of vaccinia virus DNA and were prepared from virus-infected HeLa cells. The early virosomal proteins were S-35-labelled and SDS polyacrylamide gel electrophoresis revealed the presence of three major early 35S-labelled proteins of 34, 24 and 45 kDa. The masses of molecules present in the 34 and 24 kDa proteins were measured by the convenient and sensitive MALDI TOE: mass spectroscopy technique. Identification of the three virosomal proteins was carried out by MALDI mass spectroscopy of corresponding tryptic digests. For each protein at least 13 measured masses matched, within less than 0.1 Da, calculated tryptic peptides of the vaccinia virus proteins H5R (34 kDa), E3L (24 kDa) and E5R ( 45 kDa). In addition, virosomes contained several structural proteins from the infecting virus and a 45 kDa keratin-related protein. This work demonstrates directly that the abundant early vaccinia virus proteins H5R, E3L and E5R are associated with the virosomes. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 12
页数:12
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