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Protein corona in vivo: dynamic complement proteins-mediated opsonization and immune modulation.体内蛋白质冠层:动态补体蛋白介导的调理作用和免疫调节
Sci Bull (Beijing). 2017 Jul 30;62(14):976-977. doi: 10.1016/j.scib.2017.07.002. Epub 2017 Jul 8.
2
Nanomaterial synthesis, an enabler of amyloidosis inhibition against human diseases.纳米材料合成,一种抑制人类疾病淀粉样变性的促成因素。
Nanoscale. 2020 Jul 16;12(27):14422-14440. doi: 10.1039/d0nr04273k.
3
Graphene oxide enhances β-amyloid clearance by inducing autophagy of microglia and neurons.氧化石墨烯通过诱导小胶质细胞和神经元自噬来增强β-淀粉样蛋白的清除。
Chem Biol Interact. 2020 Jul 1;325:109126. doi: 10.1016/j.cbi.2020.109126. Epub 2020 May 11.
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Molecular Mechanism for the Suppression of Alpha Synuclein Membrane Toxicity by an Unconventional Extracellular Chaperone.一种非常规细胞外伴侣抑制α-突触核蛋白膜毒性的分子机制。
J Am Chem Soc. 2020 May 27;142(21):9686-9699. doi: 10.1021/jacs.0c01894. Epub 2020 May 8.
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Immunological Responses Induced by Blood Protein Coronas on Two-Dimensional MoS Nanosheets.二维MoS纳米片上血液蛋白冠引发的免疫反应
ACS Nano. 2020 May 26;14(5):5529-5542. doi: 10.1021/acsnano.9b09744. Epub 2020 Apr 29.
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Early intraneuronal amyloid triggers neuron-derived inflammatory signaling in APP transgenic rats and human brain.早期神经元内淀粉样蛋白触发 APP 转基因大鼠和人脑源性炎症信号转导。
Proc Natl Acad Sci U S A. 2020 Mar 24;117(12):6844-6854. doi: 10.1073/pnas.1914593117. Epub 2020 Mar 6.
7
The Properties of α-Synuclein Secondary Nuclei Are Dominated by the Solution Conditions Rather than the Seed Fibril Strain.α-突触核蛋白次级核的性质主要由溶液条件决定,而不是由种子纤维应变决定。
ACS Chem Neurosci. 2020 Mar 18;11(6):909-918. doi: 10.1021/acschemneuro.9b00594. Epub 2020 Feb 28.
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Nanosilver Mitigates Biofilm Formation via FapC Amyloidosis Inhibition.纳米银通过抑制FapC淀粉样变性减轻生物膜形成。
Small. 2020 May;16(21):e1906674. doi: 10.1002/smll.201906674. Epub 2020 Jan 27.
9
Human Plasma Protein Corona of Aβ Amyloid and Its Impact on Islet Amyloid Polypeptide Cross-Seeding.β淀粉样蛋白的人血浆蛋白冠及其对胰岛淀粉样多肽交叉播种的影响
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Corona of Thorns: The Surface Chemistry-Mediated Protein Corona Perturbs the Recognition and Immune Response of Macrophages.棘冠状:表面化学介导的蛋白冠扰乱巨噬细胞的识别和免疫反应。
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淀粉样变性抑制:蛋白质冠层的新前沿

Amyloidosis Inhibition, a New Frontier of the Protein Corona.

作者信息

Chen Pengyu, Ding Feng, Cai Rong, Javed Ibrahim, Yang Wen, Zhang Zhenzhen, Li Yuhuan, Davis Thomas P, Ke Pu Chun, Chen Chunying

机构信息

Materials Research and Education Center, Auburn University, Auburn, AL 36849, United States.

Department of Physics and Astronomy, Clemson University, Clemson, SC 29634, United States.

出版信息

Nano Today. 2020 Dec;35. doi: 10.1016/j.nantod.2020.100937. Epub 2020 Jul 22.

DOI:10.1016/j.nantod.2020.100937
PMID:32728376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7388636/
Abstract

The protein corona has served as a central dogma and a nuisance to the applications of nanomedicine and nanobiotechnology for well over a decade. Here we introduce the emerging field of amyloidosis inhibition, which aims to understand and harness the interfacial phenomena associated with a nanoparticle interacting with pathogenic amyloid proteins. Much of this interaction correlates with our understanding of the protein corona, and yet much differs, as elaborated for the first time in this . Specifically, we examine the , and features of the new class of "amyloid protein corona", and discuss how the interactions with nanoparticles may halt the self-assembly of amyloid proteins. As amyloidosis is driven off pathway by the nanoparticles, the oligomeric and protofibrillar populations are suppressed to ameliorate their cytotoxicity. Furthermore, as amyloid proteins spread via the transport of bodily fluids or cross seeding, amyloidosis is inherently associated with dynamic proteins and ligands to evoke the immune system. Accordingly, we ponder the structural and medical implications of the amyloid protein corona in the presence of their stimulated cytokines. Understanding and exploiting the amyloid protein corona may facilitate the development of new theranostics against a range of debilitating amyloid diseases.

摘要

十多年来,蛋白质冠层一直是纳米医学和纳米生物技术应用的核心教条和麻烦。在此,我们介绍淀粉样变性抑制这一新兴领域,其旨在理解和利用与纳米颗粒与致病性淀粉样蛋白相互作用相关的界面现象。这种相互作用的许多方面与我们对蛋白质冠层的理解相关,但也有许多不同之处,正如本文首次阐述的那样。具体而言,我们研究了新型“淀粉样蛋白冠层”的 、 和 特征,并讨论了与纳米颗粒的相互作用如何可能阻止淀粉样蛋白的自组装。由于纳米颗粒使淀粉样变性偏离正常途径,寡聚体和原纤维群体受到抑制,从而减轻其细胞毒性。此外,由于淀粉样蛋白通过体液运输或交叉播种传播,淀粉样变性与动态蛋白质和配体固有地相关,以激发免疫系统。因此,我们思考了在受刺激的细胞因子存在下淀粉样蛋白冠层的结构和医学意义。理解和利用淀粉样蛋白冠层可能有助于开发针对一系列使人衰弱的淀粉样疾病的新型治疗诊断方法。