Xinpei Yi, Yan Fu
Cascaded database searches boost identification sensitivity in vast proteomic search spaces but challenge false discovery rate (FDR) control. The standard target-decoy approach to FDR control relies on decoy matches providing an exchangeable and properly scaled representation of incorrect target matches. This assumption can be disrupted when protein-level filtering is used to define a reduced search space, because target and decoy entries may no longer undergo symmetric retention during database reduction. Although entrapment provides an external benchmark for assessing FDR control, conventional separate-entrapment implementations can become invalid in cascaded searches because entrapment sequences may be disproportionately discarded during protein-level filtering. Here we introduce Fusion Entrapment, a strategy that computationally fuses entrapment sequences with target proteins to preserve identical selection pressure during database reduction. Simulations show that this strategy provides accurate entrapment-based false discovery proportion (FDP) estimation in cascaded searches involving protein-level filtering. Applying Fusion Entrapment to human gut metaproteomic datasets, we further observed that conventional separate target-decoy database reduction led to substantial inflation of the entrapment-estimated FDP relative to the reported FDR threshold. In contrast, fusion target-decoy reduction maintained empirical FDR control under Fusion Entrapment assessment while retaining substantial sensitivity gains over single-step analysis.