Class I hydrophobins secreted by filamentous fungi self-assemble at interfaces to form rod-like structures known as rodlets. Although hydrophobins can self-assemble at both air-water and solid-water interfaces, the mechanism governing the latter self-assembly remains poorly understood. In this study, we investigated the self-assembly of RolA, a class I hydrophobin from Aspergillus oryzae, on a polytetrafluoroethylene (PTFE) surface without an air-water interface. The fluorescence time course of thioflavin T binding indicated that RolA self-assembled at the solid-water interface. Atomic force microscopy revealed that RolA formed both rod-like structures and amorphous aggregates. The presence of such aggregates, not observed at air-water interfaces, suggests that the self-assembly pathway depends on the interface type. These findings help to advance our understanding of how the functions of hydrophobins at solid-water interfaces are related to hydrophobin self-assembly.
Building similarity graph...
Analyzing shared references across papers
Loading...
Shuma Iio
Nao Takahashi
Yuki Terauchi
Bioscience Biotechnology and Biochemistry
Kyoto University
Tohoku University
Yamaguchi University
Building similarity graph...
Analyzing shared references across papers
Loading...
Iio et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d895ea6c1944d70ce0719c — DOI: https://doi.org/10.1093/bbb/zbag051