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DC Field | Value | Language |
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dc.contributor.author | Gustiananda, Marsia | - |
dc.contributor.author | Purnama, Shawn Tjahaja | - |
dc.contributor.author | Siswanto, Melinda | - |
dc.date.accessioned | 2023-09-30T00:53:37Z | - |
dc.date.available | 2023-09-30T00:53:37Z | - |
dc.date.issued | 2019 | - |
dc.identifier.uri | http://repository.i3l.ac.id/jspui/handle/123456789/822 | - |
dc.description.abstract | T cells are the primary effector cells of tumor immunity. T cells recognized peptides derived from tumor antigens wich is presented as a complex with HLA (histocompatibility leukocyte antigen - HLA) on the surface of target cells. HLA-A*24:07 is the major HLA alleles in Indonesia. HLA A*24:07 is considered unique and not a member of the HLA A*24 supertype, which is represented by HLA A*24:02. The two molecules, A*24:02 and A*24:07, share high homology except for one amino acid residue number 70. Residue number 70 in A*24:02 is H and in A*24:07 is Q. This residue happens to be in the peptide binding groove of the HLA allele, and affecting at least 3 out of 6 peptide binding pockets. HLA-A*24:07 is a less characterized allele, and at the moment, there is only one T-cell epitopes reported to be restricted by this HLA allele (IEDB website). The paper will present the peptide binding motif of HLA A*24:07, the benchmark of online T cell epitope prediction server, and the use of prediction server to predict peptide derived from cancer antigens that will bind to HLA A*24:07 | en_US |
dc.language.iso | en | en_US |
dc.publisher | Department of Biomedicine, School of Life Sciences, Indonesia International Institute for Life Sciences | en_US |
dc.subject | T cell | en_US |
dc.subject | Cancer | en_US |
dc.subject | HLA A*24:07 | en_US |
dc.title | T cell epitope prediction of cancer antigens restricted by HLA A*24:07 | en_US |
Appears in Collections: | Biomedicine |
Files in This Item:
File | Description | Size | Format | |
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INCOB2019_HLAA2407.pdf | 1.62 MB | Adobe PDF | View/Open |
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