TY - JOUR
T1 - Profile identification of disease-associated humoral antigens using AMIDA, a novel proteomics-based technology
AU - Gires, O.
AU - Münz, M.
AU - Schaffrik, M.
AU - Kieu, C.
AU - Rauch, J.
AU - Ahlemann, M.
AU - Eberle, D.
AU - Mack, B.
AU - Wollenberg, B.
AU - Lang, S.
AU - Hofmanm, T.
AU - Hammerschmidt, W.
AU - Zeidler, R.
PY - 2004/5
Y1 - 2004/5
N2 - We describe AMIDA (autoantibody-mediated identification of antigens), a novel target identification technology based on the immunoprecipitation of disease-specific antigens by autologous serum antibodies followed by two-dimensional electrophoretic separation, and their identification via mass spectrometry. Twenty-seven potential carcinoma antigens were identified including proteins of hitherto unknown function. Validation of one of the identified antigens, cytokeratin 8, revealed its de novo expression in hyperplastic tissue, gradual overexpression with increasing malignancy, and ectopic localization on the cell surface. Furthermore, a strong prevalence of CK8-specific antibodies occurred in the serum of cancer patients already at early disease stages. In situ hybridization for one marker of unknown function, KIAA1273/TOB3, demonstrated its strong overexpression in head and neck carcinomas, thus making it a likely tumor antigen candidate. Eventually, AMIDA could foster significant improvements for the diagnosis and therapy of human diseases eliciting a humoral immune response, and allows for the rapid identification of new target molecules.
AB - We describe AMIDA (autoantibody-mediated identification of antigens), a novel target identification technology based on the immunoprecipitation of disease-specific antigens by autologous serum antibodies followed by two-dimensional electrophoretic separation, and their identification via mass spectrometry. Twenty-seven potential carcinoma antigens were identified including proteins of hitherto unknown function. Validation of one of the identified antigens, cytokeratin 8, revealed its de novo expression in hyperplastic tissue, gradual overexpression with increasing malignancy, and ectopic localization on the cell surface. Furthermore, a strong prevalence of CK8-specific antibodies occurred in the serum of cancer patients already at early disease stages. In situ hybridization for one marker of unknown function, KIAA1273/TOB3, demonstrated its strong overexpression in head and neck carcinomas, thus making it a likely tumor antigen candidate. Eventually, AMIDA could foster significant improvements for the diagnosis and therapy of human diseases eliciting a humoral immune response, and allows for the rapid identification of new target molecules.
UR - http://www.scopus.com/inward/record.url?scp=2542519935&partnerID=8YFLogxK
U2 - 10.1007/s00018-004-4045-8
DO - 10.1007/s00018-004-4045-8
M3 - Journal articles
C2 - 15141305
AN - SCOPUS:2542519935
SN - 1420-682X
VL - 61
SP - 1198
EP - 1207
JO - Cellular and Molecular Life Sciences
JF - Cellular and Molecular Life Sciences
IS - 10
ER -