• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

直接探测氧化石墨烯纳米片对 hIAPP 原纤维的解离作用。

Directly probing the dissociation effects of graphene oxide nanosheets on hIAPP fibrils.

机构信息

State Key Laboratory of Surface Physics and Department of Physics, Fudan University, Shanghai 200433, People's Republic of China. Collaborative Innovation Center of Advanced Microstructures, Nanjing 210093, People's Republic of China.

出版信息

Nanotechnology. 2018 Dec 7;29(49):495102. doi: 10.1088/1361-6528/aae143. Epub 2018 Sep 13.

DOI:10.1088/1361-6528/aae143
PMID:30211692
Abstract

The aggregation of human islet amyloid polypeptides (hIAPP) to mature fibrils is considered as the main cause of type II diabetes. Therefore destroying the pre-formed hIAPP fibrils is expected to be a promising strategy for therapeutic treatments. In this work, the dissociation effects of graphene oxide (GO) nanosheets on hIAPP mature fibrils are investigated. The results clearly demonstrate that hIAPP fibrils can be quickly adsorbed on the GO surface and efficiently broken into short fragments. Meanwhile, the β-sheet structures of hIAPP fibrils are greatly destroyed. Particularly, in situ atomic force microscopy was applied to monitor the real-time interaction between hIAPP fibrils and GO nanosheets. It provides distinct evidence that the disruption of hIAPP fibrils by GO nanosheets mainly occurs at the GO edges. Size-dependent experiments further justify the interfere of edge contribution, which suggest small-sized GO nanosheets exhibit better dissociation ability than large-sized ones. Therefore, this study not only provides valuable information that GO nanosheets (especially small-sized ones) can act as efficient nanoblades to break hIAPP fibrils, but also suggests a powerful and widely available methodology for investigating real-time interaction between nanomaterials and biomolecules.

摘要

人胰岛淀粉样多肽(hIAPP)的聚集形成成熟纤维被认为是 II 型糖尿病的主要原因。因此,破坏预先形成的 hIAPP 纤维有望成为一种有前途的治疗策略。在这项工作中,研究了氧化石墨烯(GO)纳米片对 hIAPP 成熟纤维的解离作用。结果清楚地表明,hIAPP 纤维可以快速吸附在 GO 表面上,并有效地被打断成短片段。同时,hIAPP 纤维的β-折叠结构也被大大破坏。特别地,原位原子力显微镜被应用于监测 hIAPP 纤维和 GO 纳米片之间的实时相互作用。它提供了明确的证据,表明 GO 纳米片对 hIAPP 纤维的破坏主要发生在 GO 边缘。尺寸依赖性实验进一步证明了边缘贡献的干扰,表明小尺寸的 GO 纳米片比大尺寸的具有更好的解离能力。因此,这项研究不仅提供了有价值的信息,即 GO 纳米片(特别是小尺寸的)可以作为有效的纳米刀片来打断 hIAPP 纤维,还为研究纳米材料和生物分子之间的实时相互作用提供了一种强大而广泛可用的方法。

相似文献

1
Directly probing the dissociation effects of graphene oxide nanosheets on hIAPP fibrils.直接探测氧化石墨烯纳米片对 hIAPP 原纤维的解离作用。
Nanotechnology. 2018 Dec 7;29(49):495102. doi: 10.1088/1361-6528/aae143. Epub 2018 Sep 13.
2
Graphene oxide inhibits hIAPP amyloid fibrillation and toxicity in insulin-producing NIT-1 cells.氧化石墨烯抑制胰岛素分泌型NIT-1细胞中人类胰岛淀粉样多肽的淀粉样纤维化及毒性。
Phys Chem Chem Phys. 2016 Jan 7;18(1):94-100. doi: 10.1039/c5cp05924k. Epub 2015 Dec 2.
3
The Inhibitory Effect of Hydroxylated Carbon Nanotubes on the Aggregation of Human Islet Amyloid Polypeptide Revealed by a Combined Computational and Experimental Study.羟基化碳纳米管通过计算与实验联合研究揭示对人胰岛淀粉样多肽聚集的抑制作用。
ACS Chem Neurosci. 2018 Nov 21;9(11):2741-2752. doi: 10.1021/acschemneuro.8b00166. Epub 2018 Jul 23.
4
Co-assembly of human islet amyloid polypeptide (hIAPP)/insulin.人胰岛淀粉样多肽(hIAPP)/胰岛素共组装。
Chem Commun (Camb). 2012 Jan 7;48(2):191-3. doi: 10.1039/c1cc14285b. Epub 2011 Oct 14.
5
Fluorine Functionalized Graphene Quantum Dots as Inhibitor against hIAPP Amyloid Aggregation.氟功能化石墨烯量子点作为人胰岛淀粉样多肽(hIAPP)淀粉样聚集的抑制剂
ACS Chem Neurosci. 2017 Jun 21;8(6):1368-1377. doi: 10.1021/acschemneuro.7b00015. Epub 2017 Mar 3.
6
Defining the molecular basis of amyloid inhibitors: human islet amyloid polypeptide-insulin interactions.确定淀粉样蛋白抑制剂的分子基础:人胰岛淀粉样多肽与胰岛素的相互作用。
J Am Chem Soc. 2014 Sep 17;136(37):12912-9. doi: 10.1021/ja504031d. Epub 2014 Sep 4.
7
Peptide Conjugates of Benzene Carboxylic Acids as Agonists and Antagonists of Amylin Aggregation.苯羧酸的肽缀合物作为胰淀素聚集的激动剂和拮抗剂
Bioconjug Chem. 2017 Feb 15;28(2):666-677. doi: 10.1021/acs.bioconjchem.6b00732. Epub 2017 Jan 27.
8
Zinc and pH modulate the ability of insulin to inhibit aggregation of islet amyloid polypeptide.锌和 pH 值调节胰岛素抑制胰岛淀粉样多肽聚集的能力。
Commun Biol. 2024 Jun 27;7(1):776. doi: 10.1038/s42003-024-06388-y.
9
Structural and energetic insight into the cross-seeding amyloid assemblies of human IAPP and rat IAPP.对人胰岛淀粉样多肽(IAPP)和大鼠IAPP交叉播种淀粉样聚集体的结构与能量洞察。
J Phys Chem B. 2014 Jun 26;118(25):7026-36. doi: 10.1021/jp5022246. Epub 2014 Jun 12.
10
Genistein: A Dual Inhibitor of Both Amyloid β and Human Islet Amylin Peptides.染料木黄酮:一种同时抑制淀粉样β肽和人胰岛淀粉样肽的双重抑制剂。
ACS Chem Neurosci. 2018 May 16;9(5):1215-1224. doi: 10.1021/acschemneuro.8b00039. Epub 2018 Feb 20.

引用本文的文献

1
Recent advances of two-dimensional materials in smart drug delivery nano-systems.二维材料在智能药物递送纳米系统中的最新进展。
Bioact Mater. 2020 Jul 15;5(4):1071-1086. doi: 10.1016/j.bioactmat.2020.06.012. eCollection 2020 Dec.