A New Epitope of CYP2D6 Recognized by Liver Kidney Microsomal Autoantibody from Japanese Patients with Autoimmune Hepatitis(Pharmacology)
スポンサーリンク
概要
- 論文の詳細を見る
Liver-kidney microsomal antibodies type 1 (LKM-1) are a diagnostic marker for autoimmune hepatitis type II (AIH-II). However, LKM autoantibodies are also detected in a small percentage of patients with chronic hepatitis C. The autoantigen to anti-LKM-1 has been identified to be CYP2D6. To identify the specific antigenic site of CYP2D6 for LKM-1 serum, we established an ELISA with peptides spanning the entire sequence of CYP2D6. Human CYP2D6 containing histidine tag was expressed in Escherichia coli. Purified CYP2D6 was digested by lysyl endopeptidase. The linker including the histidine tag has a lysine residue in its C-terminal and can be removed by digestion. Digested peptides were separated by reversed-phase HPLC and coated on ELISA plates chemically with glutaraldehyde. The immunoreactivity of two LKM-1-positive sera (HCV-negative) and five HCV-positive sera from Japanese patients was investigated with the plates. These sera recognized peptides 1-146, 181-214, 246-281, 284-391, and 412-429. The peptide 1-146 was recognized by LKM-1-positive sera but not HCV-positive sera and is a new epitope found in this study. Seven short peptides spanning peptide 1-146 were synthesized and ELISAs were conducted with these peptides. However, two sera recognized none of these peptides, suggesting that two LKM-1-positive sera recognize the conformational immunogenic site of peptide 1-146.
- 公益社団法人日本薬学会の論文
- 2005-12-01
著者
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HIROI Toyoko
Department of Chemical Biology, Osaka City University Graduate School of Medicine
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IMAOKA Susumu
Nanobiotechnology Research Center and Department of Bioscience, School of Science and Technology, Kw
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FUNAE Yoshihiko
Department of Chemical Biology, Osaka City University Graduate School of Medicine
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NISHIGUCHI Shuhei
Division of Hepatobiliary and Pancreatic Medicine, Department of Internal Medicine, Hyogo College of
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Hiroi Toyoko
Department Of Chemical Biology Osaka City University Graduate School Of Medicine
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FUNAE Yoshihiko
Osaka City University School of Medicine
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Nishiguchi Shuhei
Division Of Hepatobiliary And Pancreatic Disease Department Of Internal Medicine Hyogo College Of Me
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Funae Y
Osaka City Univ. Medical School Osaka Jpn
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Funae Yoshihiko
Department Of Chemical Biology Osaka City University Graduate School Of Medicine
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Funae Y
Osaka City University Medical School
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Funae Yoshihiko
Department Of Chemical Biology Osaka City University Medical School
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Imaoka S
Nanobiotechnology Research Center And Department Of Bioscience School Of Science And Technology Kwan
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Imaoka Susumu
Nanobiotechnology Res. Center And Dep. Of Bioscience School Of Sci. And Technol. Kwansei Gakuin Univ
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Imaoka Susumu
Department Of Bioscience And Nanobiotechnology Research Center School Of Science And Technology Kwan
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OSADA Mayuko
Department of Chemical Biology, Osaka City University Medical School
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OBATA Noriko
Department of Chemical Biology, Osaka City University Medical School
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HARA Rie
Nanobiotechnology Research Center and Department of Bioscience, School of Science and Technology, Kw
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Hara Rie
Nanobiotechnology Research Center And Department Of Bioscience School Of Science And Technology Kwan
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Obata Noriko
Department Of Chemical Biology Osaka City University Medical School
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Osada Mayuko
Department Of Pathological Biochemistry Kyoto Pharmaceutical University
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Nishiguchi Shuhei
Department Of Hepatology Osaka City University Medical School
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