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Inhibition of islet amyloid polypeptide (IAPP) amyloid formation and cytotoxicity via structure-based,selective N-methylation of amide bonds of amyloid core sequences

机译:胰岛淀粉样蛋白形成和细胞毒性通过基于淀粉样芯序列的酰胺键的选择性N-甲基化抑制胰岛淀粉样蛋白多肽(IAPP)淀粉样蛋白形成和细胞毒性

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摘要

Pancreatic amyloid is present in more than 95% of type II diabets patients and is formed by the aggregation of the 37-residue iselt amyloid polypeptide (IAPP).IAPP amyloid aggregates are cytotoxic and have been linked to the progressive of beta-cell function and the pathological sequelae of type II diabetes [1].
机译:胰腺淀粉样蛋白在95%的II型糖尿病患者中存在,并且通过37-残基Isel淀粉样蛋白多肽(IAPP)的聚集形成.iapp淀粉样蛋白聚集体是细胞毒性,并且已与β细胞功能的进展相关联II型糖尿病病理后遗症[1]。

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