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The CFTR-derived peptides as a model of sequence-specific protein aggregation
Cellular & Molecular Biology Letters volume 12, pages 435–447 (2007)
Protein aggregation is a hallmark of a growing group of pathologies known as conformational diseases. Although many native or mutated proteins are able to form aggregates, the exact amino acid sequences involved in the process of aggregation are known only in a few cases. Hence, there is a need for different model systems to expand our knowledge in this area. The so-called ag region was previously found to cause the aggregation of the C-terminal fragment of the cystic fibrosis transmembrane conductance regulator (CFTR). To investigate whether this specific amino acid sequence is able to induce protein aggregation irrespective of the amino acid context, we altered its position within the CFTR-derived C-terminal peptide and analyzed the localization of such modified peptides in transfected mammalian cells. Insertion of the ag region into a different amino acid background affected not only the overall level of intracellular protein aggregation, but also the morphology and subcellular localization of aggregates, suggesting that sequences other than the ag region can substantially influence the peptide’s behavior. Also, the introduction of a short dipeptide (His-Arg) motif, a crucial component of the ag region, into different locations within the C-terminus of CFTR lead to changes in the aggregation pattern that were less striking, although still statistically significant. Thus, our results indicate that even subtle alterations within the aggregating peptide can affect many different aspects of the aggregation process.
cystic fibrosis transmembrane conductance regulator
green fluorescence protein
nucleotide-binding fold 2
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Bąk, D., Cutting, G.R. & Milewski, M. The CFTR-derived peptides as a model of sequence-specific protein aggregation. Cell Mol Biol Lett 12, 435–447 (2007). https://doi.org/10.2478/s11658-007-0014-1
- Protein aggregation
- Conformational diseases
- Site-directed mutagenesis