Random phage mimotopes recognized by monoclonal antibodies against the pyruvate dehydrogenase complex-E2 (PDC-E2)

被引:18
作者
Cha, SH
Leung, PSC
VandeWater, J
Tsuneyama, K
Joplin, RE
Ansari, AA
Nakanuma, Y
Schatz, PJ
Cwirla, S
Fabris, LE
Neuberger, JM
Gershwin, ME
Coppel, RL
机构
[1] UNIV CALIF DAVIS,SCH MED,DIV RHEUMATOL ALLERGY & CLIN IMMUNOL,DAVIS,CA 95616
[2] MONASH UNIV,DEPT MICROBIOL,CLAYTON,VIC 3168,AUSTRALIA
[3] EMORY UNIV,WINSHIP CANC CTR,DEPT PATHOL,ATLANTA,GA 30322
[4] KANAZAWA UNIV,SCH MED,DEPT PATHOL,KANAZAWA,ISHIKAWA 920,JAPAN
[5] AFFYMAX RES INST,PALO ALTO,CA 94304
[6] QUEEN ELIZABETH HOSP,LIVER & HEPATOBILIARY UNIT,BIRMINGHAM B15 2TH,W MIDLANDS,ENGLAND
关键词
D O I
10.1073/pnas.93.20.10949
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dihydrolipoamide acetyltransferase, the E2 component of the pyruvate dehydrogenase complex (PDC-E2), is the autoantigen most commonly recognized by autoantibodies in primary biliary cirrhosis (PBC), We identified a peptide mimotope(s) of PDC-E2 by screening a phage-epitope library expressing random dodecapeptides in the pill coat protein of fd phage using C355.1, a murine monoclonal antibody (mAb)that recognizes a conformation-dependent epitope in the inner lipoyl domain of PDC-E2 and uniquely stains the apical region of bile duct epithelium (BDE) only in patients with PBC, Eight different sequences were identified in 36 phage clones, WMSYPDRTLRTS was present in 29 clones; WESYPFRVGTSL, APKTYVSVSGMV, LTYVSL-QGRQGH, LDYVPLKHRHRH, AALWGVKVRHVS, KVLN-RIMAGVRH and GNVALVSSRVNA were singly represented, Three common amino acid motifs (W-SYP, TYVS, and VRH) were shared among all peptide sequences, Competitive inhibition of the immunohistochemical staining of PBC BDE was performed by incubating the peptides WMSYPDRTLRTS, WESYPDRTLRTS, APKTYVSVSGMV, and AALWGVKVRHVS with either C355.1 or a second PDC-E2-specific mAb, C150.1. Both mAbs were originally generated to PDC-E2 but map to distinct regions of PDC-E2, Two of the peptides, although selected by reaction with C355.1, strongly inhibited the staining of BDE by C150.1, whereas the peptide APK-TYVSVSGMV consistently inhibited the staining of C355.1 on biliary duct epithelium more strongly than the typical mitochondrial staining of hepatocytes, Rabbit sera raised against the peptide WMSYPDRTLRTS stained BDE of livers and isolated bile duct epithelial cells of PBC patients more intensively than controls, The rabbit sera stained all size ducts in normals, but only small/medium-sized ductules in PBC livers, These studies provide evidence that the antigen present in BDE is a molecular mimic of PDC-E2, and not PDC-E2 itself.
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收藏
页码:10949 / 10954
页数:6
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