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Sari, L. M.

Publications and source records attributed to Sari, L. M..

2 recordsLinked to original sources

Discrete protein dynamics enable long-range communication

Allostery, in which perturbations at an input protein site tune the activity at a distant output site, allows proteins to serve as molecular logic gates. Often, information is transmitted without altering the structure outside of the input and output sites. This focalized allostery requires correlated motion between protein backbone dihedral angles that are separated by distances many times longer than the scale of electrostatic interactions. What physical properties of folded proteins enable such long-distance information sharing despite thermal noise is unclear. To address this question, we introduce a Variable-Well Dihedral (VWD) model Hamiltonian which removes dependence on chemical details and forces, instead only tuning the degree of nonlinearity of purely local interactions within a densely-packed polymer. We show that tuning the physical parameters of the model gives rise to focalized allostery in so far that doing so increases the discreteness of the internal degrees of freedom, with real proteins occupying the highly discrete regime. These results parallel, at the molecular scale, the superiority of digital compared to analog signal processing for telecommuncations under noisy conditions.

biophysics↗

Mechanism of MEK1 activation by phosphorylation

Phosphorylation is the most common post-translational protein modification, often acting as the activator of protein function. In the case of MEK1, a member of the MAP kinase family, phosphorylation of both S218 and S222 are necessary for activation. Yet the molecular activation mechanism and its cooperative nature are poorly understood, especially due to the lack of experimental phosphorylated MEK1 structures. We performed molecular dynamics simulations to investigate the structural and dynamical consequences of single and double phosphorylation in MEK1. We find that successive phosphorylation progressively unwinds the helix containing the phosphorylation sites, thereby rotating the phosphate groups to directly interact with the catalytic site. Consequently, the solvent accessible surface area of the catalytic residues increase with phosphorylation. Yet, only in the double-phosphorylated state do all four critical catalytic residues become solvent exposed. By calculating the conformational entropy, we find that only in the double-phosphorylated state do all four catalytic residues have mutual information with each other, suggesting that phosphorylation also induces correlated motion at the active site. To validate our approach, we show that our simulations predict the alignment of the R-spine motif in the double-phosphorylated state, in agreement with the other kinases for which this alignment has been experimentally observed. These results show that phosphorylation can, via a partial unfolding mechanism, increase the solvent exposure of and dynamical coupling within the active site, both of which are critical for enzymatic activity.

biophysics↗