Allosteric Type and Pathways Are Governed by the Forces of Protein-Ligand Binding

Allostery is central to many cellular processes, by up- or down-regulating target function. However, what determines the allosteric type remains elusive and currently it is impossible to predict whether the allosteric compounds would activate or inhibit target function before experimental studies. We demonstrated that the allosteric type and allosteric pathways are governed by the forces imposed by ligand binding to target protein using the anisotropic network model and developed an allosteric type prediction method (AlloType). AlloType correctly predicted 13 of the 16 allosteric systems in the data set with experimentally determined protein and complex structures as well as verified allosteric types, which was also used to identify allosteric pathways. When applied to glutathione peroxidase 4, a protein with no complex structure information, AlloType could still be able to predict the allosteric type of the recently reported allosteric activators, demonstrating its potential application in designing specific allosteric drugs and uncovering allosteric mechanisms.

Automated summary

The study investigated protein allostery and developed a method for predicting the type and pathways of allostery, successfully predicting the types and pathways of multiple allosteric systems. The AlloType method demonstrated potential applications in designing specific allosteric drugs and uncovering allosteric mechanisms.