Year: 2025
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide We present computer simulations of the dimerization process of three different parathyroid horomone (PTH) segments, PTH 34, PTH 42, and PTH 84 . A thermodynamic analysis reveals that the aggregation is driven and determined by the N-terminal segment PTH 34 alone. Our simulation model is a coarse-grained one but we can translate the temperature scale of our simulation to physical units by comparison of chain size with experimental data. From this, we can identify that the dimerization and concomitant chain folding occurs only slightly above physiological temperature conditions. The noncooperativity of the dimerization process and its vicinity to physiological conditions give rise to the reversibility of the aggregation of PTH and the functional use of PTH fibrils as storage devices.
Authors: C. Sommerfeld, W. Paul
Institution: Martin Luther University Halle-Wittenberg
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Funder: Deutsche Forschungsgemeinschaft
OpenAlex ID: W4416502385