Influence of repeating sequence on structural and thermal stability of crystalline domain of bombyx mori silk fibroin

Abstract

Thermophysical properties of polar-antiparallel β-sheet crystalline domains of B.mori silk fibroin has been investigated via molecular dynamics (MD) simulations between 300 K and 700 K. In general, the type of interactions determines the character of the thermal expansion in corresponding directions except that the crystalline domains with serine residue contracts along the chain direction resulting with a negative thermal expansion (NTE) coefficient of αy-10-4 K-1 at 300 K. The heat capacity at constant pressure CP increases sublinearly up to about 650 K with an almost continuous decrease in the rate of change of entropy dSdT-P Energetic behavior of the β-sheet crystalline units is determined by the main chain below 400 K then thermally activated motion of side chain (HG1) of serine residue becomes effective up to the degradation point. These are particularly important in designing thermally controlled composite materials.