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| Hauptseite > Publikationsdatenbank > Impact of Phosphorylation on the Physiological Form of Human alpha-Synuclein in Aqueous Solution > print |
| Hauptseite > Publikationsdatenbank > Impact of Phosphorylation on the Physiological Form of Human alpha-Synuclein in Aqueous Solution > print |
| 001 | 1032184 | ||
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| 100 | 1 | _ | |a de Bruyn, Emile |0 P:(DE-Juel1)184777 |b 0 |e First author |
| 245 | _ | _ | |a Impact of Phosphorylation on the Physiological Form of Human alpha-Synuclein in Aqueous Solution |
| 260 | _ | _ | |a Washington, DC |c 2024 |b American Chemical Society |
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| 520 | _ | _ | |a Serine 129 can be phosphorylated in pathological inclusions formed by the intrinsically disordered protein human α-synuclein (AS), a key player in Parkinson’s disease and other synucleinopathies. Here, molecular simulations provide insight into the structural ensemble of phosphorylated AS. The simulations allow us to suggest that phosphorylation significantly impacts the structural content of the physiological AS conformational ensemble in aqueous solution, as the phosphate group is mostly solvated. The hydrophobic region of AS contains β-hairpin structures, which may increase the propensity of the protein to undergo amyloid formation, as seen in the nonphysiological (nonacetylated) form of the protein in a recent molecular simulation study. Our findings are consistent with existing experimental data with the caveat of the observed limitations of the force field for the phosphorylated moiety. |
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