bioRxiv Science⌕ Search

Biology subjects

Diyaolu, A.

Publications and source records attributed to Diyaolu, A..

2 recordsLinked to original sources

Open-State Dynamics and Allosteric Modulation of the α1β3γ2 GABAA Receptor Stabilized by L9'T/S Substitutions

GABA type A receptors (GABAARs) mediate inhibitory neurotransmission, and their dysfunction contributes to epilepsy, anxiety, and depression. Although closed and desensitized structures of heteropentameric GABAARs are known, an open-state conformation has been difficult to capture. Here we use in-silico mutagenesis and Gaussian-accelerated MD to stabilize open-like ensembles of the 1{beta}3{gamma}2 receptor via hydrophilic substitutions at the hydrophobic 9' gate (L9'T/L9'S). The mutants expand the pore at 9' and 20' (extracellular pore entry), increase hydration and water flux, and lower Cl- permeation barriers at 9' and -2' (desensitization gate) from [~]19/[~]9 kcal mol-{superscript 1} (WT) to [~]1.3-1.6/[~]3.0-3.4 kcal mol-1, yielding ohmic conductance [~]10-30 pS in computational electrophysiology. Conformationally, the mutants show reduced twist, outward M2 tilts, and C-loop closure, consistent with activation-like signatures. On this open-like background, PAMs (diazepam, ganaxolone) primarily tune the residual -2' constriction, whereas bicuculline (orthosteric antagonist) drives a time-ordered, bottom-to-top closing sequence (-2' first, then 9'/20', then twist) via an asymmetric collapse of the M2 bundle that approaches closed-state landmarks while sampling desensitized-like ECD-TMD coupling. Two-electrode voltage clamp confirms spontaneous activity in L9'T-containing receptors, supporting the mutant-stabilized open-like ensembles. These results provide a coherent atomistic framework for gating and allosteric modulation in 1{beta}3{gamma}2 GABAARs and establish a tractable, ligand-responsive platform for state-selective structure-based design.

biophysics↗

Structural Mechanisms Underlying Distinct Binding and Activities of 18:0 and 18:1 Lysophosphatidic acids at LPA1 Receptor

Lysophosphatidic acids (LPAs) are bioactive lipids that regulate numerous physiological functions in humans. Cell signaling by LPAs is mediated mainly via six LPA receptors (LPA1-6), class A G protein-coupled receptors (GPCRs). Among these, LPA1 is recognized to play an essential role in cell proliferation, survival, migration, and tumorigenesis. Despite the structural similarity, 18:0-LPA and 18:1-LPA exhibit distinct functional responses in cell lines overexpressing LPA1. Specifically, our in vitro studies show that 18:1-LPA induces greater Erk activation than 18:0-LPA in PC-3 human prostate cancer cells. The structural basis underlying this differential receptor activation has not been previously studied. Using classical molecular dynamics and enhanced sampling techniques, we examined the access and binding mechanisms of the two LPA species to the active state LPA1 receptor. The results show that 18:0-LPA and 18:1-LPA adopt distinct and dynamic poses in the orthosteric pocket despite their similar starting configurations. Mainly, the alkyl tails of the ligands exhibit distinct orientations and residue interactions, leading to differential conformational changes in key activation switches on the conserved CWxP and PIF structural motifs of the receptor. Also, there are significant differences in interhelical interactions at the intracellular end of the transmembrane helices 1, 3, 6, and 7. These distinct arrangements lead to striking differences in LPA1 interactions with the G-helix of the heterotrimeric Gi-protein. Notably, 18:0-LPA and 18:1-LPA exhibit similar membrane partitioning characteristics and receptor entry processes through aqueous paths. Our comprehensive in-silico studies offer valuable structural insights into the observed differences in functional responses by 18:0-and 18:1-LPA.

biophysics↗