Berlin 2008 – wissenschaftliches Programm

Bereiche | Tage | Auswahl | Suche | Downloads | Hilfe

BP: Fachverband Biologische Physik

BP 25: Protein Structure and Folding

BP 25.10: Vortrag

Donnerstag, 28. Februar 2008, 16:45–17:00, PC 203

MONTECARLO SIMULATIONS OF PROTEIN FOLDING UNDER CONFINEMENT — •Pedro Armando Ojeda May¹, Aurora Londono², Nan-Yow Chen³, and Martin Garcia Rimsky¹ — ¹Kassel Universitaet, Heinrich-Plett-St- 40 34132 Kassel — ²Department of Molecular Biology, IPICYT Mexico — ³Academia Sinica, Taiwan

We present a theoretical investigation of the folding of small proteins assisted by chaperones. We describe the proteins in the framework of an effective potential model which contains the Ramachandran angles as degrees of freedom. The cage of chaperonins is modeled by an external confining potential which is also able to take into account hydrophobic and hydrophilic effects inside the cavity. Using the Wang-Landau algorithm [Phys. Rev. Lett. 86, 2050 (2001)] we determine the density of states g(E) and analyze in detail the thermodynamical properties of the confined proteins for different sizes of the cage. We show how the confinement through the chaperon dramatically reduces the phase space available for the protein leading to a much faster folding process. Slightly hydrophobic cages seem to make the native structure more stable. However, not any confining potential helps folding. If the inner walls of the cage are strongly hydrophobic, a denaturation process is induced, in which the proteins partially unfold and stick to the walls.