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This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Antigen epitopes provide valuable information useful for disease prevention, diagnosis, and treatment. Recently, more and more databases focusing on different types of epitopes have become available. Conformational epitopes are an important form of epitope formed by residues that are sequentially discontinuous but close together in three-dimensional space. These epitopes have implicit structural information, making them attractive for both theoretical and applied biomedical research. However, most existing databases focus on linear rather than conformational epitopes.
We describe CED, a special database of well defined conformational epitopes. CED provides a collection of conformational epitopes and related information including the residue make up and location of the epitope, the immunological property of the epitope, the source antigen and corresponding antibody of the epitope. All entries in this database are manually curated from articles published in peer review journals. The database can be browsed or searched through a user-friendly web interface. Most epitopes in CED can also be viewed interactively in the context of their 3D structures. In addition, the entries are also hyperlinked to various databases such as Swiss-Prot, PDB, KEGG and PubMed, providing wide background information.
A conformational epitope database called CED has been developed as an information resource for investigators involved in both theoretical and applied immunology research. It complements other existing specialised epitope databases. The database is freely available at http://web.kuicr.kyoto-u.ac.jp/~ced
Immune cells recognize epitopes (antigenic determinants) rather than entire antigens. Epitopes are the regions of an antigen that are bound by antigen-specific membrane receptors on lymphocytes or to secreted antibodies. T-cells recognize T-cell epitopes, which are usually linear peptides derived from protein antigens and presented by MHC molecules. B-cells and antibodies recognize B-cell epitopes, which can be complete, small chemical compounds or components of larger macromolecules such as nucleotides, lipids, glycans and proteins. Epitopes from macromolecules, especially proteins, are further classified into another two categories. The first, termed linear epitopes, are segments composed of a continuous string of residues along the polymer chain. The second, termed conformational epitopes, are constituted by several sequentially discontinuous segments that are brought together by the folding of the antigen into its native structure [1,2].
As the molecular basis of immune recognition and the immune response, both kinds of epitope provide valuable information that is useful for disease prevention , diagnosis[4,5], and treatment [6-10]. Many databases, focusing on different kinds of epitopes, are available as a large number of epitopes have been identified in the past 20 years. MHCPEP , SYFPEITHI, FIMM, MHCBN, EPIMHC are T cell oriented. Bcipep and Epitome are B cell oriented. AntiJen is a multifaceted database with entries on both T cell and B cell epitopes. However, most existing databases focus on linear rather than conformational epitopes.
Despite this, as many as 90% of B-cell epitopes from native proteins are conformational rather than linear [19-22]. In one report, 10 monoclonal antibodies were produced against Helicobacter pylori vacuolating cytotoxin, and all of them proved to react with conformational epitopes . As well as being very common, conformational epitopes may also have functional advantages over linear epitopes. For example, human antibodies directed to conformational epitopes neutralized a wider range of human immunodeficiency virus isolates than human antibodies directed to linear epitopes. A better understanding of conformational epitopes can not only provide useful information for new vaccine design  and new diagnostic reagent development, but also will be of great value in disease treatment, including against virus infection and cancer [6-10]. Conformational epitopes also have implicit structural information relating to the antigen itself and the mode of binding, which make them attractive to theoretical biology research.
It is money and labour intensive to identify a B cell epitope in detail experimentally. To predict B cell epitopes accurately based on sequence profiling has been a long term goal of many groups. However, a recent report by Blythe et al shows that even the best set of scales and parameters performed only marginally better than random. This suggests that structural approaches and conformational epitope prediction is vital. A conformational epitope prediction server became available recently which will help in conformational epitope discovery, but to predict conformational epitopes accurately is still a very difficult task. For this reason, only several hundred conformational epitopes are currently well defined. We would expect this number to expand rapidly in the future and so it will be necessary to have a database to store and manage all the experimentally well-defined conformational epitopes. Such a specialised conformational epitope database will also be helpful for B cell epitope prediction research.
In this paper, we describe the Conformational Epitope Database (CED). It provides a curated dataset that can be used to evaluate existing epitope prediction methods as well as develop new and better algorithms for prediction. It also complements other existing epitope databases and provides a resource for applied biomedical research in disease prevention, diagnosis, and treatment.
The MySQL relational database management system is used in CED to store, retrieve and manage the data. The web interface between the user and CED are coded in PHP with PEAR database abstraction layer support. All entries in this database are sourced from articles published in peer reviewed journals. Initially, exhaustive queries are made to PubMed and ScienceDirect; returning more than 3000 references that are loaded into an EndNote reference database. The references are then filtered manually to exclude articles that do not define a conformational epitope or where the defined epitope is only at a very low resolution or completeness. The remaining data is checked and entered manually into CED.
Each entry in CED provides information about a given conformational epitope. The information provided includes:
(1) The residue constitution and location of the epitope
(2) The immunological property of the epitope
(3) The antibody that can bind to the epitope
(4) The experimental method used to identify the epitope
(5) The source antigen where the epitope exists
(6) The sequence of the source antigen
(7) The structure of the source antigen
(8) The structure of the antigen-antibody complex
(9) The chemical properties of the source antigen
(10) The references describing the epitope
(11) The comments and miscellaneous information
Currently, CED has 225 entries. The majority (213) are epitopes from protein antigens, though the database also includes 6 from nucleic acids, 5 from glycans and 1 from lipid. 138 epitopes are from vertebrates, the majority from human (109), the rest of the epitopes are from viruses (54), bacteria (22), invertebrates (7), plants (2) and unspecified (2).
From the homepage of CED, users can find an introduction to conformational epitopes and CED. They can browse epitope records page by page and entry by entry. When browsing CED, the entries appear in a summary table at first. Only the conformational epitope ID and the constitution and location field are shown, and the data is ordered by the CED identification number (ID). Clicking on an ID opens a new window that displays the information for the selected epitope in detail. An example is shown in Figure Figure11.
Users can also search CED for specific conformational epitopes. A detailed help page for the search function is provided. CED can be searched by any field in the entry and by any combination of up to three of the fields. There are three pulldown listboxes and two pairs of radio buttons on the search interface. A query is formed by selecting one or more fields from the pulldown listbox and combining them logically by "and" or "or" radio buttons. Key words or strings, such as a partial protein sequence, the name of an antigen, PDB ID of a structure, clone code of a monoclonal antibody, author name or PMID of a reference are entered into the blank text forms. The HTML form parses the criteria into SQL database queries. The initial results returned are formatted into a summary table as described above. Selecting each ID in the summary table opens a new window that displays the detailed information of each epitope.
As an example, if one wanted to retrieve all well defined conformational epitopes from human antigens that are recognized by mouse antibodies and identified by X-ray diffraction, you would first select search field "Source antigen" from the pulldown listbox, input "human" into the corresponding blank text form and then select the "and" button. Then you would select the "Corresponding antibody" search field and input "mouse". Finally, you would select "Experimental method" and input "X-ray diffraction". The operations above will make the search interface appear as shown in Figure Figure2.2. After clicking on the "Search" button, records fulfilling the requirements would appear in a new window as shown in Figure Figure33.
Most conformational epitopes in CED can be viewed interactively in the context of the antigen-antibody complex, antigen structure or known theoretical model, if they have corresponding PDB structures. The visualization function of CED is powered by Jmol. To view an epitope in the context of its 3D structure can help users identify important structural features and judge if entries defined by non-structural methods are reasonable. When browsing or searching the CED, entries that have PDB structures will have a conspicuous view icon in both the summary table and the entry table. Clicking the view icon will initialize the loading of the Jmol Java applet. By default, structures in CED are displayed as backbone colored by secondary structure. After loading, users can turn on or turn off the epitope segments, antigen chains, and antibody chains. When turned on, epitope segments "blink" and are then displayed in spacefill mode colored by CPK. Users can also zoom in, zoom out, move, spin, and rotate the structure, or even measure distance, angle, and dihedral angle. A help page for viewing epitopes can be found through a link on the view page. An example visualisation of CE0096 is shown in Figure Figure44.
Conformational epitopes can not only provide useful information for new vaccine design  and new diagnostic reagent development , but also will be of great value in disease treatment, including against virus infection and cancer [6-10]. For example, two conformational epitopes in CED (CE0096 and CE0199) are targets of two FDA approved drugs (Herceptin and Erbitux), which are effective in treating some cancers [6,9]. We need a specialised database to store this kind of useful information. Conformational epitopes also provide structural information relating to the antigen itself, making them attractive to theoretical biology research. A recent research clearly shows the underperformance of existing linear B cell epitope prediction methods , suggesting that structural approaches and conformational epitope prediction is vital. Thus a specialised conformational epitope database will be helpful for developing new B cell epitope prediction methods.
The existing epitope databases can be classified into four main categories: T cell oriented such as MHCPEP, SYFPEITHI, FIMM, MHCBN, EPIMHC; B cell oriented such as Bcipep and Epitome; single pathogenic organism oriented such as the HIV Molecular Immunology Database  and HCV Molecular Immunology Database ; multifaceted database such as AntiJen and IEDB. IEDB is still under construction at the time of writing.
Compared with most existing epitope databases, the current size of CED is limited. However, most existing epitope databases are focused on collecting linear epitopes; whereas CED only contains conformational epitopes, which are often less well defined and are harder to identify experimentally or theoretically. Many articles report new conformational epitopes, but few are defined completely and precisely enough for inclusion in CED. Taking autoimmune epitopes as an example: In many cases, the nature of the epitopes have often been successively defined and refined from the level of whole cellular organelles (using immunofluorescence methods), to identifying the macromolecule involved (immunoblot, gene expression libraries), to epitope regions (truncated cDNAs, peptide scanning), but few are identified at the contact residue level . Since data quality is vital in bioinformatics research, the aim of CED is to provide high quality, well defined conformational epitope information. So conformational epitopes that are not defined clearly are discarded which limits the database size.
Epitome, a very recently released B cell epitope database has a similar size to CED. Epitome collects B cell epitopes only from PDB structures and includes CDR information. In contrast, CED is sourced from the literature and also has conformational epitopes defined by methods other than X-ray diffraction and NMR, such as scanning mutagenesis, overlapping peptides, and phage display. Although CED and Epitome are similar they are derived from different resources and so provide complementary information. We believe that a simple database, such as CED, specialising in conformational epitopes has value in conjunction with these more complex, less specialised, databases. Although our manual search procedure may have missed a few known conformational epitopes, we believe that CED is an essentially complete database of well defined conformational epitopes.
Firstly, like all other databases, errors will have occurred during the data accumulation phase. We hope users will send their feedback to help us maintain and revise CED in future.
Secondly, we will scan newly published peer review articles for well defined or refined conformational epitopes routinely. New epitopes will be added; and newly refined epitopes will be updated. Due to the rapid progress of techniques in this field, we expect that more and more new conformational epitopes will be identified in the future. Thus, both the quantity and quality of CED entries will increase.
Lastly, we have noticed that a formal ontology of epitopes has been developed and suggested recently. To represent and communicate epitope information systematically and effectively, we will make the next release of CED completely compatible with IEDB's ontology.
A conformational epitope database (CED) has been developed, which can be browsed or searched through a simple user friendly web interface. It is an essentially complete database of well defined conformational epitopes and provides a complement to other existing specialised epitope databases. CED is also hyperlinked to several external databases, providing wide background information for each entry. Though currently relatively small in size, the data in CED provides valuable information for disease prevention, diagnosis, and treatment. Thus, we hope it will be an important information resource for investigators involved in both theoretical and applied immunology research.
CED: Conformational Epitope Database; CDR: Complementarity-Determining Region; HCV: Hepatitis C Virus; HIV: Human Immunodeficiency Virus; HTML: Hypertext Markup Language; IEDB: Immune Epitope Database and Analysis Resource; KEGG: Kyoto Encyclopaedia of Genes and Genomes; MHC: Major Histocompatibility Complex; NCBI: National Center for Biotechnology Information; PEAR: PHP Extension and Application Repository; PDB: Protein Data Bank; PHP: Hypertext Preprocessor; SQL: Structured Query Language.
JH and WH extracted the data, compiled the database and wrote the code for the web interface. All authors have read and approved the final manuscript.
We thank Professor Kanehisa for supervising the work, our lab colleagues Dr Alex Gutteridge for copyediting the manuscript, Dr Shanfeng Zhu for useful discussion, Mr Koichiro Tonomura and Dr Nobuya Tanaka for help with coding. We also thank Professor Mackay of Monash University for permitting us to adapt their published figure to the logo of CED. The computational resources were provided by the Bioinformatics Center, Institute for Chemical Research, Kyoto University.