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Immunoglobulin Y: an IgG-like antibody with an IgE-like structure?

Reference	BB/D011418/1
Principal Investigator / Supervisor	Professor Brian Sutton
Co-Investigators / Co-Supervisors
Institution	King's College London
Department	Randall Div of Cell and Molecular Biophy
Funding type	Research
Value (£)	292,786
Status	Completed
Type	Research Grant
Start date	01/02/2006
End date	31/01/2009
Duration	36 months

Abstract

Birds, reptiles and amphibia have only one serum antibody, IgY, in contrast to mammalian IgG and IgE, and an IgY-like molecule is the evolutionary precursor of IgG and IgE. IgY takes part in opsonisation (a function associated with mammalian IgG) and in anaphylactic reactions (mediated by mammalian IgE). We propose to find out how IgY performs these two different functions. We will prepare IgY and recombinant fragments, and identify one or more of its receptors on leukocytes to investigate IgY-receptor interaction(s). We have extensively studied IgE binding to its high affinity receptor, solved the crystal structure of IgE-Fc (the receptor-binding region of the antibody), and discovered structural features of IgE that determine its characteristically slow dissociation rate from the complex; this slow off-rate confers upon IgE its unique ability to sensitise cells and trigger allergic reactions. With this experience we are ideally placed to make a comparative study of the IgY-receptor interaction, and to produce mutants to probe key features of IgY-Fc. The recent publication of the chicken genome sequence makes this an ideal time to pursue these studies. The chicken orthologues of human Th1 and Th2 cytokines have been cloned, and it has also been discovered that different infective agents can elicit production of a Th1-like or a Th2-like response. The differential response to these cytokines in the human system depends on IgG and IgE, begging the question of how the production of a single antibody IgY can lead to two different responses in the chicken. IgY-receptor interactions may well be involved in this discrimination. We have already cloned the Fc region of IgY, with 'external' glycosylation removed, to provide a homogeneous species for X-ray analysis. We have also cloned a further carbohydrate mutant, together with cysteine mutants, to investigate the effect of the conserved 'internal' glycosylation site, and inter-chain disulphide bridges, on receptor binding. Transient expression has been obtained, but stable clones need to be produced. We shall also prepare yolk and serum IgY and their Fc fragments for binding studies, as earlier work suggested that there may be functional differences with respect to anaphylaxis. We have also recently obtained two alternatively spliced full-length chicken transcripts (one with three, and one with four extracellular immunoglubulin-like domains) of a putative IgY-binding polypeptide (alpha-chain), as well as a full-length putative signalling polypeptide (gamma-chain) that contains a signalling activation motif (ITAM). Together they may constitute leukocyte IgY-Fc receptor(s), orthologue(s) of the IgG-Fc and IgE-Fc receptors, which have not yet been identified. They are cloned and ready for expression on the surface of COS cells. If IgY binding is achieved, we can then clone the soluble extracellular portion of the alpha-chain for analysis of binding kinetics, and crystallisation with our recombinant IgY-Fc. If IgY binding is not detected, we shall search the new version of the chicken genome (expected July 2005) to identify other IgG-Fc receptor orthologues, or revert to protein purification or screening a COS cell expression library, to obtain the receptor. The kinetics and affinity of the IgY-receptor interaction will be measured on cells (using purified chicken basophils and a chicken monocyte cell line) and using the BIAcore technique with the recombinant proteins. The latter will be particularly important for making precise comparisons between the different mutant versions of IgY-Fc. Together these data will provide a complete description of the IgY-receptor interaction for comparison with mammalian IgG and IgE. We have already generated most of the starting materials for this work, and are now in a very competitive position to make a contribution to this field.

Summary

The human immune system provides protection against foreign invading organisms including parasites, bacteria and viruses, through a variety of different cells, such as the white blood cells, and proteins, such as the antibodies. In man, as in other mammals, there are specialized types of antibodies: a type known as IgG deal principally with viruses and bacteria, while another, called IgE, is produced in defence against parasites. However, in regions of the world where parasitic infections no longer present a challenge, these IgE antibodies are instead produced in response to substances that we call allergens. People with a tendency to produce high levels of IgE are especially susceptible to allergies, such as hayfever, asthma and food allergies. We have been studying IgE antibodies in order to understand how they cause allergy, and have discovered that there is a particular part of the antibody molecule, present in IgE but not in IgG, which gives it special properties. In particular, it causes the IgE molecules to stick extremely tightly to cells and activate them when parasites invade the body. Although this is very effective against parasites, it unfortunately has the same effects, which include a sudden inflammation reaction, when allergens such as grass pollen, bee venom or particular foods, for example peanuts, enter the body. The effects of these sudden allergic reactions are well-known, and can even be fatal. One aim of our work in this field is to develop improved drugs to treat these conditions. There is however much that we have yet to learn about the human immune system, such as the 'polarization' into the IgG and IgE type responses, and why only certain molecules that we know as allergens provoke the IgE response. One way of approaching this is from an evolutionary standpoint. Birds do not have IgG or IgE, but instead have a single type of antibody called IgY. In fact, an IgY-like antibody was present in the last common ancestor of birds and mammals, 300 million years ago, and was the evolutionary predecessor of IgG and IgE. IgY combines in a single molecule the properties of both IgG and IgE, yet birds do respond differently to viruses and parasites in their immune response, despite having only one type of antibody. We propose to study IgY from chickens, since they have the best-studied non-mammalian immune system. The publication last year of the complete DNA sequence of the chicken genome has greatly enhanced these studies. In particular, we propose to isolate the molecules to which IgY binds on the surfaces of cells, and we are the first, to our knowledge, to have identified such a 'receptor' for IgY. We shall study how IgY binds to cells, and aim to discover how it combines the roles of both IgG and IgE, thus helping us to understand, and perhaps then prevent, the unwanted IgE allergic response in man. One of the outcomes of this research is therefore an improved understanding of the human immune system and its evolution, with future benefits for human medicine. However, improved understanding of the chicken immune system is not without its own benefits. Poultry meat is an important source of human disease, and the control of bacterial disease in chickens is largely based on an indiscriminate use of antibiotics; this over-use of antibiotics has severely reduced their usefulness in controlling human bacterial infections, as the emergence of strains of antibiotic-resistant 'super-bugs' has shown. A better understanding of the chicken immune system may lead to better ways of controlling bacterial infection in these commercially important animals. Chickens and other avian species can also harbour viruses that can in turn threaten man, such as the recent outbreak of avian 'flu, and improved knowledge of immunity in birds may help us to understand how this transmission process occurs.

Committee	Closed Committee - Biomolecular Sciences (BMS)
Research Topics	Immunology, Structural Biology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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