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Peptide Blocking CTLA-4 and B7-1 Interaction
Discovery of the B7 family immune checkpoints such as CTLA-4 (CD152), PD-1 (CD279), as well as their ligands B7-1 (CD80), B7-2 (CD86), B7-H1 (PD-L1, CD274), and B7-DC (PD-L2, CD273), has opened new possibilities for cancer immunotherapy using monoclonal antibodies (mAb). The blockade of inhibitory r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825301/ https://www.ncbi.nlm.nih.gov/pubmed/33419027 http://dx.doi.org/10.3390/molecules26020253 |
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author | Podlesnykh, Stepan V. Abramova, Kristina E. Gordeeva, Anastasia Khlebnikov, Andrei I. Chapoval, Andrei I. |
author_facet | Podlesnykh, Stepan V. Abramova, Kristina E. Gordeeva, Anastasia Khlebnikov, Andrei I. Chapoval, Andrei I. |
author_sort | Podlesnykh, Stepan V. |
collection | PubMed |
description | Discovery of the B7 family immune checkpoints such as CTLA-4 (CD152), PD-1 (CD279), as well as their ligands B7-1 (CD80), B7-2 (CD86), B7-H1 (PD-L1, CD274), and B7-DC (PD-L2, CD273), has opened new possibilities for cancer immunotherapy using monoclonal antibodies (mAb). The blockade of inhibitory receptors (CTLA-4 and PD-1) with specific mAb results in the activation of cancer patients’ T lymphocytes and tumor rejection. However, the use of mAb in clinics has several limitations including side effects and cost of treatment. The development of new low-molecular compounds that block immune checkpoints’ functional activity can help to overcome some of these limitations. In this paper, we describe a synthetic peptide (p344) containing 14 amino acids that specifically interact with CTLA-4 protein. A 3D computer model suggests that this peptide binds to the (99)MYPPPY(104) loop of CTLA-4 protein and potentially blocks the contact of CTLA-4 receptor with B7-1 ligand. Experimental data confirm the peptide-specific interaction with CTLA-4 and its ability to partially block CTLA-4/B7-1 binding. The identified synthetic peptide can be used for the development of novel immune checkpoint inhibitors that can block CTLA-4 functional activity for cancer immunotherapy. |
format | Online Article Text |
id | pubmed-7825301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78253012021-01-24 Peptide Blocking CTLA-4 and B7-1 Interaction Podlesnykh, Stepan V. Abramova, Kristina E. Gordeeva, Anastasia Khlebnikov, Andrei I. Chapoval, Andrei I. Molecules Communication Discovery of the B7 family immune checkpoints such as CTLA-4 (CD152), PD-1 (CD279), as well as their ligands B7-1 (CD80), B7-2 (CD86), B7-H1 (PD-L1, CD274), and B7-DC (PD-L2, CD273), has opened new possibilities for cancer immunotherapy using monoclonal antibodies (mAb). The blockade of inhibitory receptors (CTLA-4 and PD-1) with specific mAb results in the activation of cancer patients’ T lymphocytes and tumor rejection. However, the use of mAb in clinics has several limitations including side effects and cost of treatment. The development of new low-molecular compounds that block immune checkpoints’ functional activity can help to overcome some of these limitations. In this paper, we describe a synthetic peptide (p344) containing 14 amino acids that specifically interact with CTLA-4 protein. A 3D computer model suggests that this peptide binds to the (99)MYPPPY(104) loop of CTLA-4 protein and potentially blocks the contact of CTLA-4 receptor with B7-1 ligand. Experimental data confirm the peptide-specific interaction with CTLA-4 and its ability to partially block CTLA-4/B7-1 binding. The identified synthetic peptide can be used for the development of novel immune checkpoint inhibitors that can block CTLA-4 functional activity for cancer immunotherapy. MDPI 2021-01-06 /pmc/articles/PMC7825301/ /pubmed/33419027 http://dx.doi.org/10.3390/molecules26020253 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Podlesnykh, Stepan V. Abramova, Kristina E. Gordeeva, Anastasia Khlebnikov, Andrei I. Chapoval, Andrei I. Peptide Blocking CTLA-4 and B7-1 Interaction |
title | Peptide Blocking CTLA-4 and B7-1 Interaction |
title_full | Peptide Blocking CTLA-4 and B7-1 Interaction |
title_fullStr | Peptide Blocking CTLA-4 and B7-1 Interaction |
title_full_unstemmed | Peptide Blocking CTLA-4 and B7-1 Interaction |
title_short | Peptide Blocking CTLA-4 and B7-1 Interaction |
title_sort | peptide blocking ctla-4 and b7-1 interaction |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825301/ https://www.ncbi.nlm.nih.gov/pubmed/33419027 http://dx.doi.org/10.3390/molecules26020253 |
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