期刊
PROTEIN EXPRESSION AND PURIFICATION
卷 184, 期 -, 页码 -出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pep.2021.105879
关键词
Yeast protein expression; Protein purification; Affinity chromatography; Recombinant antibodies; Secreted proteins
类别
资金
- AIRC [IG 15627, IG 21510, 24020]
- PRIN Italian Ministry of University and Research (MIUR) Leveraging basic knowledge of ion channel network in cancer for innovative therapeutic strategies (LIONESS) [20174TB8KW]
- European Union [813834]
Protein engineering has made significant advancements in biotechnology and pharmaceuticals, particularly with the development of engineered antibody subclasses. The single chain diabody format offers versatility in a variety of applications, but challenges include optimizing production, improving expression systems, purification procedures, and stability. Fine-tuning recombinant antibody expression through choosing the right protein expression host and adjusting expression protocols is crucial for success.
In the last decades, protein engineering has developed particularly in biotechnology and pharmaceutical field. In particular, the engineered antibody subclass has arisen. The single chain diabody format (scDb), conjugating small size with antigen specificity, offers versatility representing a gold standard for a variety of applications, spacing from research to diagnostics and therapy. Along with such advantages, comes the challenge of optimizing their production, improving expression systems, purification procedures and stability. All such parameters are detrimental for protein production in general and above all for recombinant antibody expression, which has to be fine-tuned, choosing a proper protein-expression host and adjusting expression protocols accordingly. In the present paper, we present data regarding the production and purification of a single chain diabody directed against the macromolecular complex hERG1/beta 1 integrin. We focus on the expression of clones deriving from the transformation of Pichia pastoris yeast cells. In particular, we compare two different clones arose from two separate transformation processes, demonstrating that both are suitable for proper protein expression. Moreover, we have set up an expression protocol and compared the yields obtained using two purification machines: Akta Pure and Akta Start, with a positive outcome.
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