Background & Aims: Primary biliary cirrhosis (PBC) is a chronic choles
tatic liver disease characterized by the presence of antimitochondrial
autoantibodies in patients' serum. The major autoantigen, recognized
by antibodies from >95% of patients with PBC, has been identified as t
he E2 component (E2p) of the pyruvate dehydrogenase multienzyme comple
x, Immunodominant sites on E2p have been localized to the inner of the
two lipoyl domains, where the essential cofactor lipoic acid is attac
hed covalently. The aim of this study was to determine the three-dimen
sional structure of the inner lipoyl domain of human E2p. Methods: The
domain was expressed in Escherichia coli; after purification, its str
ucture was analyzed using nuclear magnetic resonance spectroscopy. Res
ults: The structure of the lipoyl domain from human E2p was determined
, and the implications of the structure for autoimmune recognition wer
e assessed. Conclusions: Knowledge of the structure further defines th
e major epitope and may help in the design of antigen-specific immunot
herapy for treatment of PBC.