PL-PatchSurfer3: Improved Structure-Based Virtual Screening for Structure Variation Using 3D Zernike Descriptors

Structure-based virtual screening (SBVS) is a widely used method in silico drug discovery. It necessitates a receptor structure or binding site to predict the binding pose and fitness of a ligand. Therefore, the performance of the SBVS is affected by the protein conformation. The most frequently used method in SBVS is the protein-ligand docking program, which utilizes atomic distance-based scoring functions. Hence, they are highly prone to sensitivity towards variation in receptor structure, and it is reported that the conformational change significantly drops the performance of the docking program. To address the problem, we have introduced a novel program of SBVS, named PL-PatchSurfer. This program makes use of molecular surface patches and the Zernike descriptor. The surfaces of the pocket and ligand are segmented into several patches by the program. These patches are then mapped with physico-chemical properties such as shape and electrostatic potential before being converted into the Zernike descriptor, which is rotationally invariant. A complementarity between the protein and the ligand is assessed by comparing the descriptors and geometric distribution of the patches in the molecules. A benchmarking study showed that PL-PatchSurfer2 was able to screen active molecules regardless of the receptor structure change with fast speed. However, the program could not achieve high performance for the targets that the hydrogen bonding feature is important such as nuclear hormone receptors. In this paper, we present the newer version of PL-PatchSurfer, PL-PatchSurfer3, which incorporates two new features: a change in the definition of hydrogen bond complementarity and consideration of visibility that contains curvature information of a patch. Our evaluation demonstrates that the new program outperforms its predecessor and other SBVS methods while retaining its characteristic tolerance to receptor structure changes. Interested individuals can access the program at [kiharalab.org/plps3][1]. ### Competing Interest Statement The authors have declared no competing interest. * SBVS : Structure-Based Virtual Screening VS : Virtual Screening LBVS : Ligand-Based Virtual Screening 3DZD : Three-Dimensional Zernike descriptor PL-PS3 : PL-PatchSurfer3 EF : Enrichment Factor DUD : Directory of Useful Decoys APBS : Adaptive Possion-Boltzmann Solver GRPD : Geodesic Relative Patch Difference APPD : Approximate Patch Position Difference APP : Approximate Patch Position LCS : Lowest Conformer Score BWS : Boltzmann-Weighted Score AUC : Area Under the receiver operating characteristic Curve BEDROC : Boltzmann-Enhanced Discrimination of Receiver Operating Characteristic [1]: https://kiharalab.org/plps3