posted on 2021-04-30, 13:36authored byVerónica A. Jiménez, Karen R. Navarrete, Mario Duque-Noreña, Kelly P. Marrugo, María A. Contreras, Cristian H. Campos, Joel B. Alderete
E-selectin
is a cell-adhesion receptor with specific recognition
capacity toward sialo-fucosylated Lewis carbohydrates present in leukocytes
and tumor cells. E-selectin interactions mediate the progress of inflammatory
processes and tumor metastasis, which aroused the interest in using
this protein as a biomolecular target to design glycomimetic inhibitors
for active targeting or therapeutic purposes. In this work, we report
the rational discovery of two novel glycomimetic peptides targeting
E-selectin based on mutations of the reference selectin-binding peptide
IELLQAR. Sixteen single or double mutants at Ile1, Leu3, Leu4, and
Arg7 residues were evaluated as potential candidates for E-selectin
targeting using 50 ns molecular dynamics (MD) simulations. Nine peptides
showing a stable association with the functional pocket were modified
by adding a cysteine residue to the N-terminus to confer versatility
for further chemical conjugation. Subsequent 50 ns MD simulations
resulted in five cysteine-modified peptides with retained or improved
E-selectin binding potential. Then, 300 ns accelerated MD (aMD) simulations
were used to examine the binding properties of the best five cysteine-modified
peptides. CIEELQAR and CIELFQAR exhibit the most selective association
with the functional pocket of E-selectin, as revealed by potential
of mean force profiles. Microscale thermophoresis experiments confirmed
the E-selectin binding capacity of the selected peptides with KD values in the low micromolar range (CIEELQAR KD = 35.0 ± 1.4 μM; CIELFQAR KD = 16.4 ± 0.7 μM), which are 25-fold
lower than the reported value for the native ligand sLex (KD = 878 μM). Our findings support
the potential of CIEELQAR and CIELFQAR as novel E-selectin-targeting
peptides with high recognition capacity and versatility for chemical
conjugation, which are critical for enabling future applications in
active targeting.