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Nucleic Acids Res ; 46(D1): D419-D427, 2018 01 04.
Article in English | MEDLINE | ID: mdl-28977646

ABSTRACT

The ability to decode antigen specificities encapsulated in the sequences of rearranged T-cell receptor (TCR) genes is critical for our understanding of the adaptive immune system and promises significant advances in the field of translational medicine. Recent developments in high-throughput sequencing methods (immune repertoire sequencing technology, or RepSeq) and single-cell RNA sequencing technology have allowed us to obtain huge numbers of TCR sequences from donor samples and link them to T-cell phenotypes. However, our ability to annotate these TCR sequences still lags behind, owing to the enormous diversity of the TCR repertoire and the scarcity of available data on T-cell specificities. In this paper, we present VDJdb, a database that stores and aggregates the results of published T-cell specificity assays and provides a universal platform that couples antigen specificities with TCR sequences. We demonstrate that VDJdb is a versatile instrument for the annotation of TCR repertoire data, enabling a concatenated view of antigen-specific TCR sequence motifs. VDJdb can be accessed at https://vdjdb.cdr3.net and https://github.com/antigenomics/vdjdb-db.


Subject(s)
Antigens/chemistry , Databases, Protein , Molecular Sequence Annotation , Receptors, Antigen, T-Cell/chemistry , Software , Amino Acid Sequence , Animals , Antigens/immunology , Antigens/metabolism , Binding Sites , High-Throughput Nucleotide Sequencing , Humans , Internet , Macaca mulatta , Major Histocompatibility Complex/genetics , Major Histocompatibility Complex/immunology , Mice , Models, Molecular , Protein Binding , Protein Interaction Domains and Motifs , Protein Structure, Secondary , Receptors, Antigen, T-Cell/immunology , Receptors, Antigen, T-Cell/metabolism , Sequence Alignment , Sequence Homology, Amino Acid , Single-Cell Analysis , T-Lymphocytes/cytology , T-Lymphocytes/immunology
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