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Development of an enabling platform biotechnology for the production of proteins.
Aschenbrenner, Isabel; Böckler, Maximilian; Franke, Fabian; Liebl, Korbinian; Catici, Dragana A M; Brandl, Matthias; Behnke, Julia; Feige, Matthias J.
Afiliación
  • Aschenbrenner I; TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), 9184 Technical University of Munich , D-85748 Garching, Germany.
  • Böckler M; TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), 9184 Technical University of Munich , D-85748 Garching, Germany.
  • Franke F; TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), 9184 Technical University of Munich , D-85748 Garching, Germany.
  • Liebl K; TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), 9184 Technical University of Munich , D-85748 Garching, Germany.
  • Catici DAM; TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), 9184 Technical University of Munich , D-85748 Garching, Germany.
  • Brandl M; TUM School of Natural Sciences, Department of Bioscience, Bavarian NMR Center (BNMRZ), 9184 Technical University of Munich , D-85748 Garching, Germany.
  • Behnke J; TUM School of Medicine, Department of Surgery, Klinikum Rechts der Isar München, 9184 Technical University of Munich , D-81675 Munich, Germany.
  • Feige MJ; TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), 9184 Technical University of Munich , D-85748 Garching, Germany.
Biol Chem ; 405(7-8): 471-483, 2024 Jul 26.
Article en En | MEDLINE | ID: mdl-38916991
ABSTRACT
Protein-based drugs are a mainstay of modern medicine. In contrast to antibodies, most of these need highly individualized production processes which often limits their development. Here, we develop an immunoglobulin domain tag (i-Tag), which can be fused to any protein of interest. This tag is made of a linear arrangement of antibody light chain constant domains. It enhances expression as well as secretion of the fusion partner and allows for simple purification of several structurally and functionally distinct fusion proteins. Furthermore, it improves the biophysical characteristics of most fusion proteins tested, is inert, and does not compromise the fusion partners' functionality. Taken together, the i-Tag should facilitate the development of biopharmaceuticals and diagnostic proteins otherwise lacking a common structural element.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biotecnología Límite: Humans Idioma: En Revista: Biol Chem Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biotecnología Límite: Humans Idioma: En Revista: Biol Chem Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Alemania