Osmolytes and Macromolecular Crowders Diversely Affect the Aggregation of the Cancerrelated L106R Mutant of the Axin RGS Domain
2020
Protein aggregation is involved in a variety
of diseases, including neurodegenerative diseases and cancer. The cellular
environment is crowded by a plethora of cosolutes comprising small molecules
and biomacromolecules at high concentrations, which may influence the
aggregation of proteins in vivo. To account for the effect of cosolutes
on cancer-related protein aggregation, we studied their effect on the
aggregation of the cancer-related L106R mutant of the Axin protein. Axin is a
key player in the Wnt signaling pathway, and the L106R mutation in its RGS
domain results in a native molten globule that tends to form native-like
aggregates. This results in uncontrolled activation of the Wnt signaling
pathway, leading to cancer. We monitored the aggregation process of Axin RGS
L106Rin vitro in the presence of a wide ensemble of cosolutes including
polyols, amino acids, betaine and polyethylene glycol (PEG) crowders. Except myo-inositol,
all polyols decreased RGS L106R aggregation, with carbohydrates exerting the
strongest inhibition. Conversely, betaine and PEGs enhanced aggregation. These
results are consistent with the reported effects of osmolytes and crowders on
the stability of molten globular proteins and with both amorphous and amyloid
aggregation mechanisms. We suggest a model of Axin L106R aggregation in vivo, whereby molecularly small
osmolytes keep the protein as a free solublemolecule but the increased crowding
of the bound state by macromolecules induces its aggregation at the nano-scale.
Our study sheds light on the potential contribution of cosolutes to the onset
of cancer as a protein misfolding disease, and on the relevance of aggregation
in the molecular aetiology of cancer.
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