The construction and identification of the PRNP vectors with ubiquitin or the lysosome-targeting signal.
- Author:
Yuan LI
1
;
Guo-yong MEI
;
Hui-ying JIANG
;
Gui-rong WANG
;
Chan TIAN
;
Cao CHEN
;
Xin WANG
;
Ke-xia WANG
;
Jun HAN
;
Xiao-ping DONG
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Blotting, Western; CHO Cells; COS Cells; Cercopithecus aethiops; Cricetinae; Cricetulus; Genetic Vectors; genetics; immunology; Humans; Lysosomes; chemistry; Prion Proteins; Prions; genetics; immunology; Recombinant Proteins; genetics; immunology; Transfection; Ubiquitin; genetics; immunology
- From: Chinese Journal of Experimental and Clinical Virology 2008;22(6):419-421
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo evaluate PrP expression characteristic of PRNP nucleic acid vaccine vector with ubiquitin or the lysosome-targeting signal.
METHODSThe gene of ubiquitin and lysosome-targeting signal were ligated to PRNP and pcDNA3.1 vector that is, pcDNA3.1-UPrP and pcDNA3.1-PrPL were constructed. The expression characteristics of PrP with two signals were evaluated by Western Blot and the localization was observed by indirect immune fluorescence.
RESULTSThe protein expressed by pcDNA3.1-UPrP and pcDNA3.1-PrPL with ubiquitin and lysosome-targeting signal can be recognized by prion-specific antibody. The protein has three glycosylation molecules form as native PrP.PrP with ubiquitin was degraded gradually with time extension,whereas quantity of PrP with lysosome signal reduced in 48 h after transfection. The protein with two location signals can direct fusion proteins to cytoplasm.
CONCLUSIONThe PRNP vectors with ubiquitin or the lysosome-targeting signal were constructed and expressed in eukaryocyte successfully. There will be one of good foundation on PRNP nucleic acid vaccine.