Effect of water networks on ligand binding : computational predictions vs experiments

Szalai, Tibor Viktor (avtor), Bajusz, Dávid (avtor), Börzsei, Rita (avtor), Zsidó, Balázs Zoltán (avtor), Ilaš, Janez (avtor), Ferenczy, György G. (avtor), Hetényi, Csaba (avtor), Keserü M., György (avtor)

Rational drug design focuses on the explanation and prediction of complex formation between therapeutic targets and small-molecule ligands. As a third and often overlooked interacting partner, water molecules play a critical role in the thermodynamics of protein–ligand binding, impacting both the entropy and enthalpy components of the binding free energy and by extension, on-target affinity and bioactivity. The community has realized the importance of binding site waters, as evidenced by the number of computational tools to predict the structure and thermodynamics of their networks. However, quantitative experimental characterization of relevant protein–ligand–water systems, and consequently the validation of these modeling methods, remains challenging. Here, we investigated the impact of solvent exchange from light (H$_2$O) to heavy water (D$_2$O) to provide complete thermodynamic profiling of these ternary systems. Utilizing the solvent isotope effects, we gain a deeper understanding of the energetic contributions of various components. Specifically, we conducted isothermal titration calorimetry experiments on trypsin with a series of p-substituted benzamidines, as well as carbonic anhydrase II (CAII) with a series of aromatic sulfonamides. Significant differences in binding enthalpies found between light vs heavy water indicate a substantial role of the binding site water network in protein–ligand binding. Next, we challenged two conceptually distinct modeling methods, the grid-based WaterFLAP and the molecular dynamics-based MobyWat, by predicting and scoring relevant water networks. The predicted water positions accurately reproduce those in available high-resolution X-ray and neutron diffraction structures of the relevant protein–ligand complexes. Estimated energetic contributions of the identified water networks were corroborated by the experimental thermodynamics data. Besides providing a direct validation for the predictive power of these methods, our findings confirmed the importance of considering binding site water networks in computational ligand design.

• Jezik: Angleški jezik
• Ključne besede: ligands, molecular structure, molecules, peptides and proteins, screening assays
• Vrsta gradiva: Članek v reviji
• Tipologija: 1.01 - Izvirni znanstveni članek
• Organizacija: FFA - Fakulteta za farmacijo
• Različica publikacije: Objavljena publikacija
• Leto izida: 2024
• Št. strani: Str. 8980-8998
• Številčenje: Vol. 64, no. 23
• PID: 20.500.12556/RUL-165845
• UDK: 542.9:615
• ISSN pri članku: 1549-960X
• DOI: 10.1021/acs.jcim.4c01291291
• COBISS.SI-ID: 218384643
• Datum objave v RUL: 12.12.2024

Gradivo je del revije

• Naslov: Journal of chemical information and modeling
• Založnik: Amrican Chemical Society
• ISSN: 1549-960X
• COBISS.SI-ID: 3037204

Licence

• Licenca: CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
• Povezava: http://creativecommons.org/licenses/by/4.0/deed.sl
• Opis: To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

• Jezik: Slovenski jezik
• Ključne besede: ligandi, molekularna struktura, molekule, peptidi in proteini, presejalni testi