TY - JOUR
T1 - A structural protein of hepatitis C virus expressed in E. coli facilitates accurate detection of hepatitis C virus
AU - Muraiso, Kanae
AU - Hijikata, Makoto
AU - Ohkoshi, Showgo
AU - Cho, Myung Je
AU - Kikuchi, Masayoshi
AU - Kato, Nobuyuki
AU - Shimotohno, Kunitada
N1 - Funding Information:
ACKNOWLEDGMENTS: This study was supported by Grants-in-Aid Cancer Research and for a Comprehensive lo-Year Strategy Cancer Control from the Ministry of Health and Welfare, K.M. and M.H. are the recipients of Research Resident Fellowships from the Foundation for Promotion of Cancer Research. We thank M. Ohara for helpful comments.
PY - 1990/10/30
Y1 - 1990/10/30
N2 - A putative core protein derived from hepatitis C virus was expressed in E. coli. More than 5% of the total protein expressed in the bacteria after induction by isopropylthio-beta-D-galactoside was shown to be the expected protein. Western blotting with this E. coli lysate proved to be more efficient than ELISA with a non-structural viral protein, C100, to detect infection of hepatitis C virus in the sera of patients with non-A, non-B chronic hepatitis, hepatocellular carcinoma as well as in sera from healthy persons.
AB - A putative core protein derived from hepatitis C virus was expressed in E. coli. More than 5% of the total protein expressed in the bacteria after induction by isopropylthio-beta-D-galactoside was shown to be the expected protein. Western blotting with this E. coli lysate proved to be more efficient than ELISA with a non-structural viral protein, C100, to detect infection of hepatitis C virus in the sera of patients with non-A, non-B chronic hepatitis, hepatocellular carcinoma as well as in sera from healthy persons.
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U2 - 10.1016/0006-291X(90)90702-O
DO - 10.1016/0006-291X(90)90702-O
M3 - Article
C2 - 1700704
AN - SCOPUS:0025109548
SN - 0006-291X
VL - 172
SP - 511
EP - 516
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -