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. 2024;25(8):638-650.
doi: 10.2174/0113892037297012240408063250.

Structural Insights of PD-1/PD-L1 Axis: An In silico Approach

Affiliations

Structural Insights of PD-1/PD-L1 Axis: An In silico Approach

Shishir Rohit et al. Curr Protein Pept Sci. 2024.

Abstract

Background: Interaction of PD-1 protein (present on immune T-cell) with its ligand PD-L1 (over-expressed on cancerous cell) makes the cancerous cell survive and thrive. The association of PD-1/PD-L1 represents a classical protein-protein interaction (PPI), where receptor and ligand binding through a large flat surface. Blocking the PD-1/PDL-1 complex formation can restore the normal immune mechanism, thereby destroying cancerous cells. However, the PD-1/PDL1 interactions are only partially characterized.

Objective: We aim to comprehend the time-dependent behavior of PD-1 upon its binding with PD-L1.

Methods: The current work focuses on a molecular dynamics simulation (MDs) simulation study of apo and ligand bound PD-1.

Results: Our simulation reveals the flexible nature of the PD-1, both in apo and bound form. Moreover, the current study also differentiates the type of strong and weak interactions which could be targeted to overcome the complex formation.

Conclusion: The current article could provide a valuable structural insight about the target protein (PD-1) and its ligand (PD-L1) which could open new opportunities in developing small molecule inhibitors (SMIs) targeting either PD-1 or PD-L1.

Keywords: PD-1/PD-L1 interactions; PD-1: Programmed cell death protein-1; PD-L1: programmed death ligand-1; immune T-cell; molecular dynamics simulations; protein-protein interaction..

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References

    1. Esfahani K.; Roudaia L.; Buhlaiga N.; Del Rincon S.V.; Papneja N.; Miller W.H.; A review of cancer immunotherapy: From the past, to the present, to the future. Curr Oncol 2020,27(12),87-97 - DOI - PubMed
    1. Pardoll D.M.; The blockade of immune checkpoints in cancer immunotherapy. Nat Rev Cancer 2012,12(4),252-264 - DOI - PubMed
    1. Hoos A.; Development of immuno-oncology drugs — from CTLA4 to PD1 to the next generations. Nat Rev Drug Discov 2016,15(4),235-247 - DOI - PubMed
    1. Khalil D.N.; Smith E.L.; Brentjens R.J.; Wolchok J.D.; The future of cancer treatment: Immunomodulation, CARs and combination immunotherapy. Nat Rev Clin Oncol 2016,13(5),273-290 - DOI - PubMed
    1. Ishida Y.; Agata Y.; Shibahara K.; Honjo T.; Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death. EMBO J 1992,11(11),3887-3895 - DOI - PubMed

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