Proteins, in the presence of trivalent cations, exhibit
intriguing
phase behavior which is contrasting compared to mono- and divalent
cations. At room temperature (RT), trivalent cations induce microscopic
liquid–liquid phase separation (LLPS) in which a protein-rich
phase coexists with a dilute phase. The critical solution temperature
related phenomena in these complex fluids are well studied; however,
such studies have mostly been restricted below the denaturation temperature
(T
M) of the protein(s) involved. Here,
we probe the phase behavior of bovine serum albumin (BSA) incubated
at 70 °C (>T
M) in the presence
of
Na+, Mg2+, La3+, Y3+,
and Ho3+ ions. BSA in the presence of mono- and bivalent
ions forms an intense gel phase at 70 °C; however, the trivalent
salts offer remarkable thermal resistivity and retain the fluid LLPS
phase. We determine the microscopic phase behavior using differential
interference contrast optical microscopy, which shows that the LLPS
droplet structures in the M3+ ion-containing protein solutions
prevail upon heating, whereas Mg2+ forms composed cross-linking
gelation upon thermal incubation. We probe the interior environment
of the protein aggregates by ps-resolved fluorescence anisotropy measurements
using 8-anilino-1-naphthalenesulfonic acid (ANS) as an extrinsic fluorophore.
It reveals that while the LLPS phase retains the rotational time constants
upon heating, in the case of gelation, the immediate environment of
ANS gets significantly perturbed. We investigate the explicit protein
hydration at RT as well as at T > T
M using the ATR THz-FTIR (1.5–22.5 THz) spectroscopy
technique and found that hydration shows strong ion specificity and
correlates the phase transition behavior.