TY - JOUR
T1 - Production of the bullous pemphigoid antigen 230 (BP230) by Saccharomyces cerevisiae and Pichia pastoris
AU - Laffitte, Emmanuel
AU - Shafaatian, Reza
AU - Fontao, Lionel
AU - Favre, Bertrand
AU - Koster, Jan
AU - Saurat, Jean Hilaire
AU - Monod, Michel
AU - Borradori, Luca
N1 - Funding Information: The authors are indebted to Dr. J.R. Stanley (University of Pennsylvania, Philadelphia) and Dr. T. Hashimoto (Keyo University School of Medicine, Tokyo) for providing antibodies used in this study, Dr. A. Sonnenberg (The Netherlands Cancer Institute, Amsterdam) for fruitful discussions as well as Mrs. B. Léchenne for skillful technical help. The study has been supported by grants from the Swiss National Foundation for Scientific Research (32.56727.99), Téléthon Action Suisse, the V Framework Programme of the European Community (QLG1-CT2001-02007), and the Office fédéral de l’éducation et de la science (OFES No. 01.0113).
PY - 2003/6/1
Y1 - 2003/6/1
N2 - BP230 is a cytoskeletal linker protein of 2649 amino acids originally identified as the target autoantigen in bullous pemphigoid, a potentially devastating autoimmune skin blistering disorder. To better define its function, we sought to generate recombinant forms of BP230 in both Saccharomyces cerevisiae and Pichia pastoris after cloning its entire cDNA. By immunoblot analysis, full-length BP230 was not found in extracts of P. pastoris, whereas minor amounts of degraded BP230 were detected in extracts of S. cerevisiae. In contrast, both S. cerevisiae and P. pastoris were able to produce the 770-amino acid COOH-terminal domain of BP230. Furthermore, the production level of the recombinant BP230 tail in S. cerevisiae was significantly higher than that observed in P. pastoris and that of endogenous BP230 in cultured human keratinocytes. Finally, 12 of 17 (71%) BP sera recognized the recombinant BP230 protein in yeast extracts. Our results indicate that S. cerevisiae occasionally constitutes a better tool for recombinant protein production than P. pastoris. Although both its large size and poor solubility limit production of BP230, the developed yeast system provides cellular fractions enriched in BP230 recombinant proteins that constitute useful tools for the diagnosis of bullous pemphigoid.
AB - BP230 is a cytoskeletal linker protein of 2649 amino acids originally identified as the target autoantigen in bullous pemphigoid, a potentially devastating autoimmune skin blistering disorder. To better define its function, we sought to generate recombinant forms of BP230 in both Saccharomyces cerevisiae and Pichia pastoris after cloning its entire cDNA. By immunoblot analysis, full-length BP230 was not found in extracts of P. pastoris, whereas minor amounts of degraded BP230 were detected in extracts of S. cerevisiae. In contrast, both S. cerevisiae and P. pastoris were able to produce the 770-amino acid COOH-terminal domain of BP230. Furthermore, the production level of the recombinant BP230 tail in S. cerevisiae was significantly higher than that observed in P. pastoris and that of endogenous BP230 in cultured human keratinocytes. Finally, 12 of 17 (71%) BP sera recognized the recombinant BP230 protein in yeast extracts. Our results indicate that S. cerevisiae occasionally constitutes a better tool for recombinant protein production than P. pastoris. Although both its large size and poor solubility limit production of BP230, the developed yeast system provides cellular fractions enriched in BP230 recombinant proteins that constitute useful tools for the diagnosis of bullous pemphigoid.
UR - http://www.scopus.com/inward/record.url?scp=0037791684&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/S1046-5928(03)00057-3
DO - https://doi.org/10.1016/S1046-5928(03)00057-3
M3 - Article
C2 - 12767802
SN - 1046-5928
VL - 29
SP - 141
EP - 147
JO - Protein Expression and Purification
JF - Protein Expression and Purification
IS - 2
ER -