F fibril types (Fig. 7). This is supported by the lack of both thioT binding and conversion to b-sheet structure. At this micellar concentration, although there is no formation of thioT reactive SDS-soluble aggregates, SDS-insoluble aggregates are still formed. These aggregates have a substantially different morphology, appearing amorphous in structure, however they are still CASIN biological activity formed via interactions of the polyQ tract, as formation of these aggregates is inhibited by QBP1 (Fig. 3A). The formation of different aggregate morphologies is not unprecedented as environmental conditions affect the type of aggregate formed by a number of proteins in vitro [49,50]. Within the cell such changes in the intracellular environment could be achieved by conditions of stress, such as elevated temperature or decreased pH, or changes in membrane composition [34,51]. Ataxin-3 oligomers and fibrils displayed a specificity in binding to PtdIns with varying degrees of phosphorylation. PtdIns are generally located on the cytoplasmic side of the plasma membrane and are present in specific membranes depending on phosphorylation, with a higher abundance of these lipids (10 ) in brainAggregation of Ataxin-3 in SDSFigure 6. Binding of polyglutamine proteins to phospholipids. (A) Protein-lipid overlays of ataxin-3(Q64) at 24 hrs (i) and 200 hrs (ii), Josephin domain at 70 hrs (iii) and 200 hrs (iv), and monomeric SpA (v) and SpA(Q52) (vi). A representative membrane is shown. (B) A summary of three independent experiments, with a fully shaded square representing strong binding in all experiments, and a triangle representing weak binding in one or two membranes only. Spot 16 is not included as it is a blank dot. doi:10.1371/journal.pone.0069416.gFigure 7. Summary of effects of SDS on ataxin-3 aggregation. Schematic summarizing the effects of micellar and non-micellar SDS on both stages of ataxin-3 aggregation. doi:10.1371/journal.pone.0069416.gAggregation of Ataxin-3 in SDStissue [52]. Although monomeric huntingtin also bound similar phospholipids [33], it appears that this is not a common polyQ specific effect as only fibrillar species of ataxin-3 showed binding. Furthermore, when the polyQ-binding peptide QBP1 was added there was no change to the binding pattern which suggests that binding occurs through the Josephin domain. This is similarly seen in the SDS experiments in this study, where the effect of SDS on the Josephin domain is identical to that on ataxin-3, and unaffected by QBP1. Phospholipids have been demonstrated to affect aggregating proteins by creating regions which have a local environment with a decreased pH, and through electrostatic interactions which can increase the local concentration of protein at the membrane and induce partial unfolding of proteins [53?5]. It is interesting that oligomers and fibrillar ataxin-3 bound to the lipid overlay with different specificities as several studies show that oligomers have a generic 10236-47-2 supplier ability to permeabilize cell membranes by creating pores or single channels within membranes [56?8]. Overall, our findings demonstrate the sensitivity of ataxin-3 fibril formation to solution conditions 23977191 and suggest a possible role for lipid molecules in the development of SCA3. The specificity of binding with only fibrillar species associating with phosphorylated phospholipids provides a link between ataxin-3 and the growing evidence that soluble oligomers disrupt membranes as part of the mechanism of toxicity within amyloidose.F fibril types (Fig. 7). This is supported by the lack of both thioT binding and conversion to b-sheet structure. At this micellar concentration, although there is no formation of thioT reactive SDS-soluble aggregates, SDS-insoluble aggregates are still formed. These aggregates have a substantially different morphology, appearing amorphous in structure, however they are still formed via interactions of the polyQ tract, as formation of these aggregates is inhibited by QBP1 (Fig. 3A). The formation of different aggregate morphologies is not unprecedented as environmental conditions affect the type of aggregate formed by a number of proteins in vitro [49,50]. Within the cell such changes in the intracellular environment could be achieved by conditions of stress, such as elevated temperature or decreased pH, or changes in membrane composition [34,51]. Ataxin-3 oligomers and fibrils displayed a specificity in binding to PtdIns with varying degrees of phosphorylation. PtdIns are generally located on the cytoplasmic side of the plasma membrane and are present in specific membranes depending on phosphorylation, with a higher abundance of these lipids (10 ) in brainAggregation of Ataxin-3 in SDSFigure 6. Binding of polyglutamine proteins to phospholipids. (A) Protein-lipid overlays of ataxin-3(Q64) at 24 hrs (i) and 200 hrs (ii), Josephin domain at 70 hrs (iii) and 200 hrs (iv), and monomeric SpA (v) and SpA(Q52) (vi). A representative membrane is shown. (B) A summary of three independent experiments, with a fully shaded square representing strong binding in all experiments, and a triangle representing weak binding in one or two membranes only. Spot 16 is not included as it is a blank dot. doi:10.1371/journal.pone.0069416.gFigure 7. Summary of effects of SDS on ataxin-3 aggregation. Schematic summarizing the effects of micellar and non-micellar SDS on both stages of ataxin-3 aggregation. doi:10.1371/journal.pone.0069416.gAggregation of Ataxin-3 in SDStissue [52]. Although monomeric huntingtin also bound similar phospholipids [33], it appears that this is not a common polyQ specific effect as only fibrillar species of ataxin-3 showed binding. Furthermore, when the polyQ-binding peptide QBP1 was added there was no change to the binding pattern which suggests that binding occurs through the Josephin domain. This is similarly seen in the SDS experiments in this study, where the effect of SDS on the Josephin domain is identical to that on ataxin-3, and unaffected by QBP1. Phospholipids have been demonstrated to affect aggregating proteins by creating regions which have a local environment with a decreased pH, and through electrostatic interactions which can increase the local concentration of protein at the membrane and induce partial unfolding of proteins [53?5]. It is interesting that oligomers and fibrillar ataxin-3 bound to the lipid overlay with different specificities as several studies show that oligomers have a generic ability to permeabilize cell membranes by creating pores or single channels within membranes [56?8]. Overall, our findings demonstrate the sensitivity of ataxin-3 fibril formation to solution conditions 23977191 and suggest a possible role for lipid molecules in the development of SCA3. The specificity of binding with only fibrillar species associating with phosphorylated phospholipids provides a link between ataxin-3 and the growing evidence that soluble oligomers disrupt membranes as part of the mechanism of toxicity within amyloidose.
