N-glycosylation and ubiquitinylation of PD-L1 do not restrict interaction with BMS-202: A molecular modeling study

Comput Biol Chem. 2020 Oct:88:107362. doi: 10.1016/j.compbiolchem.2020.107362. Epub 2020 Aug 19.

Abstract

The Programmed cell Death protein-1/Ligand 1 (PD-1/L1) checkpoint is a major target in oncology. Monoclonal antibodies targeting PD-1 or PD-L1 are used to treat different types of solid tumors and lymphoma. PD-L1-binding small molecules are also actively searched. The lead compound is the biphenyl drug BMS-202 which stabilizes PD-L1 protein dimers and displays a potent antitumor activity in experimental models. Here we have investigated the effect of N-glycosylation (at N35, N192, N200 and N219) and mono-ubiquitination (at K178) of PD-L1 on the interaction with BMS-202 by molecular modeling. Two complementary tridimensional models of PD-L1, based on available crystallographic structures, were constructed with BMS-202 bound. The structures were glycosylated, with a fucosylated bi-antennary N-glycan and ubiquitinated. Model 1 refers to glycoPD-L1 bearing 16 N-glycans, with or without 4 ubiquitin residues. Model 2 presents 8 N-glycans and 2 ubiquitin residues. In both cases, BMS-202 was bound to the protein interface, stabilizing a PD-L1 dimer. The incorporation of the N-glycans or the ubiquitins did not significantly alter the drug-protein recognition. The interface of the drug-stabilized protein dimer is unaffected by the glycosylation or ubiquitination. Calculations of the binding energies indicated that the glycosylation slightly reduces the stability of the drug-protein complexes but does not prevent the drug binding process. Our modeling study suggests that the drug can target efficiently the different forms of PD-L1 in cells, glycosylated, ubiquitinated or not. These models of N-glycosylated and ubiquitinated PD-L1 will be useful to study other PD-L1 protein complexes.

Keywords: BMS-202; Drug-protein binding; Molecular modelling; PD-L1; Protein glycosylation; Ubiquitin.

MeSH terms

  • Acetamides / chemistry
  • Acetamides / pharmacology*
  • B7-H1 Antigen / chemistry
  • B7-H1 Antigen / metabolism*
  • Glycosylation
  • Humans
  • Models, Molecular
  • Molecular Structure
  • Pyridines / chemistry
  • Pyridines / pharmacology*
  • Ubiquitination

Substances

  • Acetamides
  • B7-H1 Antigen
  • BMS202
  • CD274 protein, human
  • Pyridines