Kumar Sunil, Brown Mark A, Nath Abhinav, Miranker Andrew D
Department of Molecular Biophysics and Biochemistry, Yale University, 260 Whitney Avenue, New Haven, CT 06520-8114, USA.
Department of Molecular Biophysics and Biochemistry, Yale University, 260 Whitney Avenue, New Haven, CT 06520-8114, USA.
Chem Biol. 2014 Jun 19;21(6):775-81. doi: 10.1016/j.chembiol.2014.05.007. Epub 2014 Jun 12.
Islet amyloid polypeptide (IAPP) is a hormone cosecreted with insulin by pancreatic β cells. Upon contact with lipid bilayers, it is stabilized into a heterogeneous ensemble of structural states. These processes are associated with gains of function, including catalysis of β sheet-rich amyloid formation, cell membrane penetration, loss of membrane integrity, and cytotoxicity. These contribute to the dysfunction of β cells, a central component in the pathology and treatment of diabetes. To gain mechanistic insight into these phenomena, a related series of substituted oligoquinolines were designed. These inhibitors are unique in that they have the capacity to affect both solution- and phospholipid bilayer-catalyzed IAPP self-assembly. Importantly, we show that this activity is associated with the oligoquinoline's capacity to irreversibly adopt a noncovalent fold. This suggests that compact foldamer scaffolds, such as oligoquinoline, are an important paradigm for conformational manipulation of disordered protein state.
胰岛淀粉样多肽(IAPP)是一种与胰岛素由胰腺β细胞共同分泌的激素。与脂质双层接触后,它会稳定形成结构状态各异的集合体。这些过程伴随着功能的获得,包括富含β折叠的淀粉样蛋白形成的催化、细胞膜穿透、膜完整性丧失以及细胞毒性。这些因素导致β细胞功能障碍,而β细胞功能障碍是糖尿病病理和治疗的核心组成部分。为了深入了解这些现象的机制,设计了一系列相关的取代寡喹啉。这些抑制剂的独特之处在于它们有能力影响溶液和磷脂双层催化的IAPP自组装。重要的是,我们表明这种活性与寡喹啉不可逆地形成非共价折叠的能力有关。这表明紧凑的折叠体支架,如寡喹啉,是对无序蛋白质状态进行构象操纵的重要范例。