Diverse Native Ensembles Dictate the Differential Functional Responses of Nuclear Receptor Ligand-Binding Domains

Native states of folded proteins are characterized by a large ensemble of conformations whose relative populations and interconversion dynamics determine the functional output. This is more apparent in transcription factors that have evolved to be inherently sensitive to small perturbations, thus fine-tuning gene expression. To explore the extent to which such functional features are imprinted on the folding landscape of transcription factor ligand-binding domains (LBDs), we characterize paralogous LBDs of the nuclear receptor (NR) family employing an energetically detailed and ensemble-based Ising-like statistical mechanical model. We find that the native ensembles of the LBDs from glucocorticoid receptor, PPA gamma, and thyroid hormone receptor display a remarkable diversity in the width of the native wells, the number and nature of partially structured states, and hence the degree of conformational order. Monte Carlo simulations employing the full state representation of the ensemble highlight that many of the functional conformations coexist in equilibrium, whose relative populations are sensitive to both temperature and the strength of ligand binding. Allosteric modulation of the degree of structure at a coregulator binding site on ligand binding is shown to arise via a redistribution of populations in the native ensembles of glucocorticoid and PPA. LBDs. Our results illustrate how functional requirements can drive the evolution of conformationally diverse native ensembles in paralogs.

Automated summary

The research findings show that different paralogous transcription factors' ligand-binding domains (LBDs) have diverse native ensembles, including varying widths of native wells, different numbers and natures of partially structured states, and varying degrees of conformational order. Additionally, Monte Carlo simulations reveal that many functional conformations coexist in equilibrium, with their relative populations sensitive to both temperature and the strength of ligand binding. Furthermore, allosteric modulation of the degree of structure at a coregulator binding site on ligand binding is achieved through the redistribution of populations in the native ensembles of glucocorticoid and PPA LBDs.