The gelation mechanism of β-lactoglobulin (bLG) aqueous solutions was investigated by dynamic light scattering (DLS) and small-angle neutron scattering (SANS). Temperature- and pressure-jump experiments, respectively, abbreviated as
T-jump (from 20 to 75 °C;
T-jump) and
P-jump (from 0.1 to 315 MPa) were carried out and the time evolution of gel structure was monitored by DLS and SANS as a function of time. The gelation threshold was determined by DLS as the point when nonergodicity appeared. In the case of
T-jump, a rapid increase of the time-average scattered intensity,
IT, and a steep decrease of the initial amplitude of the intensity–intensity time correlation function,
, were observed at the gelation threshold. On the other hand,
P-jump showed a gradual increase of the
IT and a continuous decrease of the
. It was revealed by SANS that bLG underwent thermal denaturation, resulting in a formation of gels consisting of densely aggregated unfolded bLG oligomers. On the other hand, the pressure-induced gels were found to be a fractal aggregates consisting of primary particles of bLG monomers. The difference in the gel structure as well as gelation mechanism between bLGs treated by
T-jump and
P-jump is discussed in comparison with
T-induced and
P-induced microphase separation of amphiphilic block copolymers in water [Osaka N, Shibayama M. Phys Rev Lett 2006;96:048303].