Novel peptide—based inhibitor for targeted inhibition of T cell function
| العنوان: | Novel peptide—based inhibitor for targeted inhibition of T cell function |
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| المؤلفون: | Ashna Gauthaman, Sneha Pasupati, C. George Priya Doss, Anbalagan Moorthy, Rini Jacob, Abarna Rajadurai |
| المصدر: | J Cell Commun Signal |
| بيانات النشر: | Springer Science and Business Media LLC, 2021. |
| سنة النشر: | 2021 |
| مصطلحات موضوعية: | Cell physiology, Chemistry, Kinase, T cell, Cell Biology, Biochemistry, Cell biology, Transactivation, Immune system, medicine.anatomical_structure, medicine, Cytokine secretion, Signal transduction, Protein kinase A, Molecular Biology, Research Article |
| الوصف: | Novel immunosuppressants are sought to overcome the side effects of currently used drugs. T cells play a central role in the functioning of the immune system; hence, drugs that specifically inhibit T cell function are expected to be better immunosuppressants with fewer side effects than the ones currently used. Peptides that interfere with crucial protein–protein interactions (PPIs) have been shown to influence cell physiology and have therapeutic potential. In this study, we designed a peptide, GVITAA, which specifically inhibits the function of lymphocyte-specific protein kinase (LCK), a signaling molecule that is mainly expressed in T cells and is responsible for positively regulating T cell function. Aspartate Histidine -Histidine Cysteine (DHHC21) -LCK is an important PPI present in T cells; DHHC21 interacts with LCK and targets the kinase to membrane rafts by adding a palmitoyl group. GVITAA is a ten amino acid peptide that interferes with the DHHC21-LCK interaction, prevents the membrane localization of LCK, and inhibits LCK-mediated initiation of complex signal transduction pathways required for T cell activation. In this study, we present evidence that the GVITAA peptide when conjugated with a cell-penetrating peptide—human immunodeficiency virus transactivator of transcription (TAT) and incubated with mouse T cells specifically inhibits LCK-mediated T cell receptor signaling, cytokine secretion, and T cell proliferation. This peptide does not affect other non-T cell functions and is non-toxic. A similar strategy was also tested and demonstrated in human peripheral T cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12079-021-00660-0. |
| تدمد: | 1873-961X 1873-9601 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93a6b55371e548a50ebc47f50e28da22 https://doi.org/10.1007/s12079-021-00660-0 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.doi.dedup.....93a6b55371e548a50ebc47f50e28da22 |
| قاعدة البيانات: | OpenAIRE |
Find this article in full text from Springer Verlag. | تدمد: | 1873961X 18739601 |
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