Production of bifunctional proteins by Aspergillus awamori: Llama variable heavy chain antibody fragment (V-HH) R9 coupled to Arthromyces ramosus peroxidase (ARP)

V. Joosten, M.S. Roelofs, N. van den Dries, T. Goosen, C.T. Verrips, C.A.M.J.J. van den Hondel, B.C. Lokman

Research output: Contribution to journalArticleAcademicpeer-review

21 Citations (Scopus)

Abstract

The Arthromyces ramosus peroxidase gene (arp) was genetically fused to either the 5'- or 3'-terminal ends of the gene encoding llama variable heavy chain antibody fragment V-HH R9, resulting in the fusion expression cassettes ARP-R9 or R9-ARP. Aspergillus awamori transformants were obtained which produced up to 30 mg 1(-1) fusion protein in the culture medium. Both fusion proteins showed peroxidase activity in an ABTS activity test. Considerable amounts of fusion protein were detected intracellularly, suggesting that the fungus encounters problems in secreting these kind of proteins. ELISA experiments showed that APP-R9 was less able to bind its antigen, the azo-dye RR6, as compared to R9-ARP. Furthermore, in contrast to R9-ARP, ARP-R9 bound to RR6 did not show peroxidase activity anymore. These results indicate that fusion of ARP to the C-terminus of the antibody fragment VHH R9 (R9-ARP) is the preferred orientation.
Original languageEnglish
Pages (from-to)347-359
JournalJournal of Biotechnology
Volume120
Issue number4
DOIs
Publication statusPublished - 2005

Keywords

  • saccharomyces-cerevisiae
  • endoplasmic-reticulum
  • filamentous fungi
  • heterologous expression
  • thaumatin production
  • light-chains
  • gene
  • secretion
  • fusion
  • domain

Fingerprint Dive into the research topics of 'Production of bifunctional proteins by Aspergillus awamori: Llama variable heavy chain antibody fragment (V-HH) R9 coupled to Arthromyces ramosus peroxidase (ARP)'. Together they form a unique fingerprint.

  • Cite this