Delta PSA: A New Metric for Conformational Dynamics Underlying Macrocyclic Peptide Permeability
Yu, Y.; Wu, Q.; Chem, J.; She, Y.; Zhu, L.; Guo, Z.
Show abstract
Development of oral cyclic drugs often suffers from low oral bioavailability resulting from limited passive permeability making accurate prediction a central challenge in drug development. Existing approaches generally fall into two categories: deep learning-based models and accelerated molecular dynamics (aMD) simulations. While deep learning models enable rapid, high-throughput predictions, they often suffer from dependence on training data, and sensitivity to dataset biases. On the other hand, aMD provide mechanistic interpretability by explicitly modeling peptide translocation across lipid bilayers, however, suffer from huge computational cost. Here, we present a conventional MD-based framework for predicting macrocyclic peptide permeability, designed to facilitate interpretation. Importantly, we show that Delta PSA ({Delta}PSA) directly quantifies a peptides chameleon propensity, providing a mechanistically meaningful measure. Furthermore, we identify two key structural indicators--the sidechain PSA ratio and the radius of gyration--as refined metrics for assessing conformational behavior. When applied to a benchmark dataset of macrocyclic peptides, our framework achieves an MSE of 0.22, surpassing the 0.25 reported for Multi_CycGT and demonstrating its superior performance. Our work also provides a large dataset of MD trajectories for macrocyclic peptides in both polar and nonpolar environments. This dataset offers access to a broader conformational space for cyclic peptide studies. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=97 SRC="FIGDIR/small/697862v2_ufig1.gif" ALT="Figure 1"> View larger version (35K): org.highwire.dtl.DTLVardef@18fc9e4org.highwire.dtl.DTLVardef@10fbc70org.highwire.dtl.DTLVardef@1c763aorg.highwire.dtl.DTLVardef@95d9e4_HPS_FORMAT_FIGEXP M_FIG C_FIG
Matching journals
The top 7 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Computational Insights into Membrane Disruption by Cell-Penetrating Peptides 95%
- A Binary Matrix Method to Enumerate, Hierarchically Order and Structurally Classify Peptide Aggregation 95%
- Investigating Ligand-Mediated Conformational Dynamics of Pre-miR21: A Machine-Learning-Aided Enhanced Sampling Study 95%
Similar papers in this journal
- Computational Modeling of Stapled Coiled-Coil Inhibitors Against Bcr-Abl: Toward a Treatment Strategy for CML 96%
- A computational model to unravel the function of amyloid-β peptide in contact with a phospholipid membrane 95%
- Investigating the effect of POPC-POPG Lipid Bilayer Composition on PAP248-286 Binding using CG Molecular Dynamics Simulations 95%
Similar papers in this journal
- Active Participation of Membrane Lipids in Inhibition of Multidrug Transporter P-Glycoprotein 94%
- Water-Glycan Interactions Drive the SARS-CoV-2 Spike Dynamics: Insights into Glycan-Gate Control and Camouflage Mechanism 93%
- Molecular mechanism of SARS-CoV-2 cell entry inhibition via TMPRSS2 by Camostat and Nafamostat mesylate 93%
Similar papers in this journal
- Energy landscapes and heat capacity signatures for monomers and dimers of amyloid forming hexapeptides 94%
- A deep dive into VDAC1 conformational diversity using all-atom simulations provides new insights into the structural origin of the closed states 94%
- Conformational Space of the Translocation Domain of Botulinum Toxin: Atomistic Modeling and Mesoscopic Description of the Coiled-Coil Helix Bundle 93%
Similar papers in this journal
- Effects of phosphorylation on protein backbone dynamics and conformational preferences 95%
- Simulated tempering-enhanced umbrella sampling improves convergence of free energy calculations of drug membrane permeation 93%
- A benzene-mapping approach for uncovering cryptic pockets in membrane-bound proteins 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.