Research focus
The occurrence of bona fide antibodies devoid of light chains in Camelidae was one of the major discoveries within our department. These so-called heavy-chain antibodies (HCAbs) bind antigens solely with one single variable domain, referred to as VHH. Methods were developed to clone the VHH repertoire of an immunized dromedary (or llama) in phage display vectors, and to select the antigen-specific VHHs from these “immune” VHH libraries. Our current research activities on camelid HCAbs and VHHs aims at three goals: (i) to increase the fundamental knowledge of VHH characteristics and HCAb ontogeny, (ii) to broaden the efficacy of VHHs and extend their applications in medical or biotechnological fields where the unique VHH properties offer a clear advantage over other antibody formats, and (iii) to develop new VHH selection strategies that are amenable to a high throughput mode. The objective here is to arrive at a rapid identification of small molecular probes to be employed in biosensors, functional genomics, structural genomics and proteomics. Obviously, the appearance of HCAbs requires the acquisition of multiple events to allow their generation and maturation into functional molecules. The dromedary germline genes (V, D and J) and constant immunoglobulin genes used to generate HCAbs were cloned. Analysis of these genes forms the cornerstone for understanding the HCAb ontogeny in camelids, and might eventually lead to the generation of a Xeno-mouse producing camel HCAbs. The antigen-specific VHHs we retrieved already have excellent biophysical properties (antigen affinity, specificity, solubility, stability, small size, recognition of epitopes that are less immunogenic for conventional antibodies). We obtained the crystal structure of many VHHs in complex with their antigen, and this forms the basis for further engineering of the VHHs to develop more versatile small molecular units. These small units are used as building blocks for more complex constructs, which are being tested as probe in biosensors, for tumor targeting, etc.
Publications
Modulation of protein properties in living cells using nanobodiesKirchhofer A, Helma J, Schmidthals K, Frauer C, Cui S, Karcher A, Pellis M, Muyldermans S, Casas-Delucchi C, Cardoso M, Leonhardt H, Hopfner K, Rothbauer UNATURE STRUCTURAL & MOLECULAR BIOLOGY, 17, 133-8, 2010 Experimental therapy of African trypanosomiasis with a nanobody-conjugated human trypanolytic factorBaral T, Magez S, Stijlemans B, Conrath K, Vanhollebeke B, Pays E, Muyldermans S, De Baetselier PNATURE MEDICINE, 12, 580-4, 2006
News
05/04/2012 - Flemish scientists have succeeded, for the first time, in developing a technology that can distinguish between different types of arterial stenosis. Their discovery is an important step in the prevention of heart attacks and sudden death. 09/04/2006 - Researchers from the Flanders Interuniversity Institute for Biotechnology (VIB) connected to the Free University of Brussels are making strides in the battle against this disease
 Serge MuyldermansResearch area(s)BioPh.D.: Vrije Universiteit Brussel, Brussels, Belgium, 1982 VIB Group leader since 1996 Contact Info
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