Imaging and quantifying analysis the binding behavior of PD-L1 at molecular resolution by atomic force microscopy
Autor: | Christian Rankl, Jilin Tang, Xinyue Guo, Yanxue Guan, Miaomiao Zhang, Zongjia Li, Juan Qin |
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Rok vydání: | 2021 |
Předmět: |
Programmed cell death
biology Atomic force microscopy Chemistry medicine.medical_treatment Force spectroscopy Immunotherapy Molecular resolution Microscopy Atomic Force Biochemistry B7-H1 Antigen Analytical Chemistry PD-L1 Neoplasms biology.protein Biophysics medicine Environmental Chemistry Molecule Humans Antibody Spectroscopy |
Zdroj: | Analytica chimica acta. 1191 |
ISSN: | 1873-4324 |
Popis: | Immunotherapy has emerged as an effective treatment modality for cancer. The interaction of programmed cell death ligand-1 (PD-L1) and programmed cell death protein-1 (PD-1) plays a key role in tumor-related immune escape and has become one of the most extensive targets for immunotherapy. Herein, we investigated the interaction of PD-L1 with its antibody and PD-1 using atomic force microscopy-based single molecule force spectroscopy for the first time. It was found that the PD-L1/anti-PD-L1 antibody complex was easier to dissociate than PD-L1/PD-1. The unbinding forces of specific interaction of PD-L1 on T24 cells with its antibody and PD-1 were quantitatively measured and similar to those on substrate. In addition, the location of PD-L1 on T24 cells was mapped at the single-molecule level by force-volume mapping. The force maps revealed that PD-L1 randomly distributed on T24 cells surface. The recognition events on cells obviously increased after INF-γ treatment, which proved that INF-γ up-regulated the expression of PD-L1 on T24 cells. These findings enrich our understanding of the molecular mechanisms by which PD-L1 interacts with its antibody and PD-1. It provides useful information for the physical factors that is needed to be considered in the design of inhibitors for tumor immunology. |
Databáze: | OpenAIRE |
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