Expression of Human Papillomavirus Type 16, Prototype and Natural Variant E7 Proteins using Baculovirus Expression System.
- Author:
Hee Sung HAN
;
Sun Ho KEE
;
Hyung Jun KIM
;
Kyung A CHO
;
Yoon Won KIM
;
Min Kee CHO
;
Woo Hyun CHANG
;
Soon Bong HWANG
- Publication Type:Original Article
- Keywords:
Human papillomavirus type 16 (HPV-16);
Prototype and natural variant;
E7;
Expression;
Subcellular localization
- MeSH:
Asparagine;
Baculoviridae*;
Blotting, Western;
Chromatin;
Cytoplasm;
Humans*;
Immunoprecipitation;
Insects;
Open Reading Frames;
Phosphoproteins;
Serine;
Sf9 Cells
- From:Journal of the Korean Society of Virology
1998;28(1):53-62
- CountryRepublic of Korea
- Language:English
-
Abstract:
Human papillomavirus (HPV) 16, E7 proteins derived from the prototype (Bac73) and natural variant (Bac101) E7 open reading frame were produced in Sf9 insect cells. The variant E7 gene occurred naturally by substitution mutation at the position of 88 nucleotide, resulting serine instead of asparagine. Using E7 specific monoclonal antibody (VD6), both E7 proteins were identified in recombinant baculovirus infected SF9 cells. Radiolabelling and immunoprecipitation analysis revealed that both E7 proteins were phosphoproteins. Immunostaining result showed that E7 proteins were mainly localized in the cytoplasm. Nuclear form of E7 proteins was also detected after a sequential fractionation procedure for removing chromatin structure. Considering that the VD6 recognition site in E7 protein is located within 10 amino acid at the N-terminus, this region appears to be blocked by the nuclear component. Western blot analysis revealed that nuclear form was more abundant than cytoplasmic E7 proteins. Time course immunostaining showed that the primary location of E7 protein was the nucleus and exported to the cytoplasm as proteins were accumulated. These events occurred similarly in both Bac73 and Bac101 infected Sf9 cells, suggesting that these two proteins may have similar biological functions.
