| Literature DB >> 27665170 |
Dayana Cabral da Silva1, Giselle N Fontes2, Luiza C S Erthal1, Luís Maurício T R Lima3.
Abstract
Amylin is a pancreatic peptide hormone co-secreted along with insulin by the β-cells. It is found in amyloid deposits in both type 2 diabetic individuals and elder non-diabetic. The triple proline amylinomimetic compound (25,28,29-Pro-human amylin) named pramlintide was designed aiming to solve the solubility and amyloid characteristics of human amylin. We have found by using ion mobility spectrometry-based mass spectrometry that pramlintide is able to assembly into multimers. Pramlintide formed amyloid fibrils in vitro in a pH-dependent kinetic process within a few hours, as followed by thioflavin T, quantification of soluble peptide and further characterized by transmission electron microscopy, atomic force microscopy and X-ray diffraction. These data indicate that pramlintide can form amyloid fibers.Entities:
Keywords: Amylin; Amyloid; Diabetes; Islet associated polypeptide; Pramlintide
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Year: 2016 PMID: 27665170 DOI: 10.1016/j.bpc.2016.09.007
Source DB: PubMed Journal: Biophys Chem ISSN: 0301-4622 Impact factor: 2.352