Predicting and Experimentally Validating Hot-Spot Residues at Protein-Protein Interfaces

Ibarra, Amaurys A.; Bartlett, Gail J.; Hegedus, Zsofia [Hegedüs, Zsófia (gyógyszerkémia), szerző]; Dutt, Som; Hobor, Fruzsina; Horner, Katherine A.; Hetherington, Kristina; Spence, Kirstin; Nelson, Adam; Edwards, Thomas A.; Woolfson, Derek N.; Sessions, Richard B. ✉; Wilson, Andrew J. ✉

Angol nyelvű Tudományos Szakcikk (Folyóiratcikk)
Megjelent: ACS CHEMICAL BIOLOGY 1554-8929 1554-8937 14 (10) pp. 2252-2263 2019
  • SJR Scopus - Medicine (miscellaneous): D1
Azonosítók
Szakterületek:
    Protein-protein interactions (PPIs) are vital to all biological processes. These interactions are often dynamic, sometimes transient, typically occur over large topographically shallow protein surfaces, and can exhibit a broad range of affinities. Considerable progress has been made in determining PPI structures. However, given the above properties, understanding the key determinants of their thermodynamic stability remains a challenge in chemical biology. An improved ability to identify and engineer PPIs would advance understanding of biological mechanisms and mutant phenotypes and also provide a firmer foundation for inhibitor design. In silico prediction of PPI hot-spot amino acids using computational alanine scanning (CAS) offers a rapid approach for predicting key residues that drive protein-protein association. This can be applied to all known PPI structures; however there is a trade-off between throughput and accuracy. Here we describe a comparative analysis of multiple CAS methods, which highlights effective approaches to improve the accuracy of predicting hot-spot residues. Alongside this, we introduce a new method, BUDE Alanine Scanning, which can be applied to single structures from crystallography and to structural ensembles from NMR or molecular dynamics data. The comparative analyses facilitate accurate prediction of hot-spots that we validate experimentally with three diverse targets: NOXA-B/MCL-1 (an alpha-helix-mediated PPI), SIMS/SUMO, and GKAP/SHANK-PDZ (both beta-strand-mediated interactions). Finally, the approach is applied to the accurate prediction of hot-spot residues at a topographically novel Affimer/BCL-x(L) protein-protein interface.
    Hivatkozás stílusok: IEEEACMAPAChicagoHarvardCSLMásolásNyomtatás
    2020-12-01 03:34