Authors
Hou, Y., Zhang, Y., Liu, Z., Peng, X., Liu, Z., Yusupujiang, M., Xu, Y., Hu, J., Liu, Z., Yang, S.
Abstract
Cyclic peptides can engage extended protein interfaces, but sequence changes that improve developability often disrupt the selected target-bound geometry. Existing property-guided design methods lack a principled way to preserve this geometry during local multiproperty optimization. Here we present RF-PepTune, which separates structural eligibility from property prioritization. Before any property score is queried, RF-PepTune evaluates single substitutions and all position-distinct pairs induced by admitted substitutions to build a parent-specific, pair-complete admission graph. Pareto Monte Carlo tree search then optimizes predicted permeability, solubility, non-fouling, and low-haemolysis scores exclusively within this graph, and selected sequences undergo full structural re-evaluation. In a matched three-arm comparison of 334 parents across MDM2, GABARAP, and MCL1, joint property-structure success rose from 10.2% without admission to 51.5% with single-substitution admission and 77.5% with pair-complete admission; pair-complete gating improved success by 26.0 percentage points over single-substitution gating (95% CI, 20.7-31.4). Property-positive but structure-failing endpoints fell from 88.3% to 9.3%. In a separate target-balanced set, all 90 prioritized outputs improved all four model-native scores while satisfying prespecified structural criteria. This work establishes pairwise structural gating as a general strategy for constrained multi-objective molecular optimization.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 01 Oct 2026.
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