Protein Aggregation and Amyloid Fibril Formation by an SH3 Domain Probed by Limited Proteolysis

• Published in: Journal of molecular biology 2003-11, Vol.334 (1), p.129-141
• Main Authors: Polverino de Laureto, Patrizia, Taddei, Niccolò, Frare, Erica, Capanni, Cristina, Costantini, Silvia, Zurdo, Jesús, Chiti, Fabrizio, Dobson, Christopher M., Fontana, Angelo
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Amyloid - metabolism; amyloid fibrils; Animals; Cattle; Circular Dichroism; Endopeptidase K - metabolism; limited proteolysis; Microscopy, Electron; Models, Molecular; Pepsin A - metabolism; Peptide Fragments - chemistry; Peptide Fragments - metabolism; Phosphatidylinositol 3-Kinases - chemistry; Phosphatidylinositol 3-Kinases - genetics; Phosphatidylinositol 3-Kinases - metabolism; protein aggregation; Protein Denaturation; Protein Structure, Tertiary; SH3 domain; Spectrometry, Fluorescence; src Homology Domains
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1016/j.jmb.2003.09.024

The SH3 domains are small protein modules of 60–85 amino acid residues that are found in many proteins involved in intracellular signal transduction. The SH3 domain of the p85α subunit of bovine phosphatidylinositol 3′-kinase (PI3-SH3) under acidic solution adopts a compact denatured state from which amyloid fibrils are readily formed. This aggregation process has been found to be modulated substantially by solution conditions. Here, we have analyzed the conformational features of the native and acid denatured states of PI3-SH3 by limited proteolysis experiments using proteinase K and pepsin, respectively. Moreover, we have analyzed the propensity of PI3-SH3 to be hydrolyzed by pepsin at different stages in the process of aggregation and amyloid formation at pH 1.2 and 2.0 and compared the sites of proteolysis under these conditions with the conformational features of both native and aggregated PI3-SH3. The results demonstrate that the denatured state of PI3-SH3 formed at low pH is relatively resistant to proteolysis, indicating that it is partially folded. The long loop connecting β-strands b and c in the native protein is the region in this structure most susceptible to proteolysis. Remarkably, aggregates of PI3-SH3 that are formed initially from this denatured state in acid solution display enhanced susceptibility to proteolysis of the long loop, suggesting that the protein becomes more unfolded in the early stages of aggregation. By contrast, the more defined amyloid fibrils that are formed over longer periods of time are completely resistant to proteolysis. We suggest that the protein aggregates formed initially are relatively dynamic species that are able readily to reorganize their interactions to enable formation of very well ordered fibrillar structures. In addition, the disordered and non-native character of the polypeptide chains in the early aggregates could be important in determining the high cytotoxicity that has been revealed in previous studies of these species.