Literature DB >> 10209277

Comparison of physical chemical properties of llama VHH antibody fragments and mouse monoclonal antibodies.

R H van der Linden1, L G Frenken, B de Geus, M M Harmsen, R C Ruuls, W Stok, L de Ron, S Wilson, P Davis, C T Verrips.   

Abstract

Antigen specific llama VHH antibody fragments were compared to antigen specific mouse monoclonal antibodies with respect to specificity, affinity and stability. The llama VHH antibody fragments and the mouse monoclonal antibodies investigated were shown to be highly specific for the protein antigen hCG or the hapten antigen RR-6. The affinity of the interaction between monovalent llama VHH antibody fragments and their antigen is close to the nanomolar range, similar to the bivalent mouse monoclonal antibodies studied. Llama VHH antibody fragments are similar to mouse monoclonal antibodies with respect to antigen binding in the presence of ammonium thiocyanate and ethanol. The results show that relative to antigen specific mouse monoclonal antibodies, antigen specific llama VHH fragments are extremely temperature stable. Two out of six llama VHHs are able to bind antigen specifically at temperatures as high as 90 degrees C, whereas four out of four mouse monoclonal antibodies are not functional at this temperature. Together with the finding that llama VHH fragments can be produced at high yield in Saccharomyces cerevisiae, these findings indicate that in the near future antigen specific llama VHH fragments can be used in for antibodies unexpected products and processes.

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Year:  1999        PMID: 10209277     DOI: 10.1016/s0167-4838(99)00030-8

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  119 in total

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3.  The role of intra-domain disulfide bonds in heat-induced irreversible denaturation of camelid single domain VHH antibodies.

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Review 4.  Nanobodies as Probes for Protein Dynamics in Vitro and in Cells.

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6.  Protein production in Yarrowia lipolytica via fusion to the secreted lipase Lip2p.

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Journal:  Mol Biotechnol       Date:  2014-01       Impact factor: 2.695

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Journal:  J Biol Chem       Date:  2013-11-07       Impact factor: 5.157

8.  Role of a noncanonical disulfide bond in the stability, affinity, and flexibility of a VHH specific for the Listeria virulence factor InlB.

Authors:  Matthew N Mendoza; Mike Jian; Moeko T King; Cory L Brooks
Journal:  Protein Sci       Date:  2020-02-08       Impact factor: 6.725

9.  Structure and specificity of several triclocarban-binding single domain camelid antibody fragments.

Authors:  Sofia Tabares-da Rosa; Linda A Wogulis; Mark D Wogulis; Gualberto González-Sapienza; David K Wilson
Journal:  J Mol Recognit       Date:  2018-07-23       Impact factor: 2.137

Review 10.  Past, present, and future of anti-IgE biologics.

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