NanobodiesApril 2011 Molecule of the Month by David Goodsell
doi: 10.2210/rcsb_pdb/mom_2011_4 (ePub Version )
Nature is full of exceptions, and sometimes they turn out to be exceptionally useful. In 1993, researchers discovered that camels, dromedaries and llamas have unusual antibodies composed of a single type of protein chain. Later, similar single-chain antibodies were discovered in sharks. This would have been just another biological oddity, but it turns out that these unusual molecules hold the key to better tools for biotechnology and medicine.
The antibodies in our blood, and in most other vertebrate animals, are composed of two types of chains (shown here on the left). The larger heavy chain (in blue) plays two roles. It comes together with another heavy chain, forming the stem of the Y-shaped antibody. It also associates with two smaller light chains (in green), which together create the antigen-binding site at the tips of each arm. Some of the antibodies in camels, however, do without the light chains entirely (shown on the right). The two arms are composed of a truncated version of the heavy chain, and the single domain in each arm does all the work of recognizing antigens.
Fragments of antibodies are widely used in technology and medicine. The arms are cut off, forming smaller molecules known as Fabs. Each Fab contains a single site for binding to their target molecules. If this Fab binds to a cell surface protein, it can be used as a diagnostic tool to identify damaged or malignant cells. If this Fab is connected to a fluorescent molecule, it can be used to image the location of its target molecule inside cells. If the Fab binds to a viral protein, it can be used as a drug to fight the virus. Unfortunately, Fab molecules are rather large, and since they are composed of two chains, they are not as stable as we would like for these applications. This is where nanobodies come in.
Nanobodies are similar fragments taken from the unusual camel antibodies. The arms are cut off, creating a smaller, more stable molecule that, like an antibody Fab, is highly specific for a given target molecule. The one shown here binds specifically to lysozyme (PDB entry 1mel). The nanobody is shown in blue and lysozyme is shown in red. Researchers have already used them in research, and are currently exploring them for use as drugs.
click on the image for an interactive Jmol
Exploring the Structure
Since nanobodies are so small, they typically interact with a smaller portion of their targets when compared to other antibodies. This turns out to be an advantage, as seen by comparing the structure of a nanobody bound to lysozyme (PDB entry 1mel) and a typical antibody Fab bound to the same target (PDB entry 1mlc). The nanobody has a finger-shaped loop that pokes into the active site of lysozyme, forming interactions that mimic the substrate. The typical antibody, however, has a large cup-shaped binding site that can't fit into the active site, so it grips one side of the protein instead. Click on the image to explore these two structures along with the structures of a shark nanobody and the lysozyme substrate.
- S. Muyldermans, T. N. Baral, V. Cortez Retamozzo, P. De Baetselier, E. De Genst, J. Kinne, H. Leonhardt, S. Magez, V. K. Nguyen, H. Revets, U. Rothbauer, B. Stijlemans, S. Tillib, U. Wernery, L. Wyns, Gh. Hassanzadeh-Ghassabeh and D. Saerens (2009) Camelid immunoglobulins and nanobody technology. Veternary Immunology and Immunopathology 128, 178-183.
- J. Wesolowski, V. Alzogaray, J. Reyelt, M. Unger, K. Juarez, M. Urrutia, A. Cauerhff, W. Danquah, F. Scheuplein, N. Schwarz, S. Adriouch, O. Boyer, M. Seman, A. Licea, D. V. Serreze, F. A. Goldbaum, F. Haag and F. Koch-Nolte (2009) Single domain antibodies: promising experimental and therapeutic tools in infection and immunity. Medical Microbiology and Immunology 198, 157-174.
- C. Hamers-Casterman, T. Atarhouch, S. Muyldermans, G. Robinson, C. Hamers, E. Bajyana Songa, N. Bendahman and R. Hamers (1993) Naturally occuring antibodies devoid of light chains. Nature 363, 446-448.
Related PDB IDs
© 2013 David Goodsell & RCSB Protein Data Bank