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利用金属氧化物纳米颗粒偶联抗体的二次离子质谱进行多重蛋白质成像。

Multiplex Protein Imaging with Secondary Ion Mass Spectrometry Using Metal Oxide Nanoparticle-Conjugated Antibodies.

机构信息

Department of New Biology, DGIST, Daegu 42988, Republic of Korea.

Department of Energy Science and Engineering, DGIST, Daegu 42988, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2020 Apr 15;12(15):18056-18064. doi: 10.1021/acsami.9b21800. Epub 2020 Feb 19.

Abstract

In spite of recent developments in mass spectrometry imaging techniques, high-resolution multiplex protein bioimaging techniques are required to unveil the complex inter- and intracellular biomolecular interactions for accurate understanding of life phenomena and disease mechanisms. Herein, we report multiplex protein imaging with secondary ion mass spectrometry (SIMS) using metal oxide nanoparticle (MONP)-conjugated antibodies with <300 nm spatial resolution in the low ion dose without ion beam damage because of the high secondary ion yields of the MONPs, which can provide simultaneous imaging of several proteins, especially from cell membranes. We applied our new imaging technique for the study of hippocampal tissue samples from control and Alzheimer's disease (AD) model mice; the proximity of protein clusters in the hippocampus CA1 region showed intriguing dependence on aging and AD progress, suggesting that protein cluster proximity may be helpful for understanding pathological pathways in the microscopic cellular level.

摘要

尽管质谱成像技术在最近取得了进展,但仍需要高分辨率的多iplex 蛋白质生物成像技术来揭示复杂的细胞内和细胞间生物分子相互作用,以准确理解生命现象和疾病机制。在此,我们报告了使用金属氧化物纳米颗粒(MONP)缀合抗体的二次离子质谱(SIMS)进行多iplex 蛋白质成像,在低离子剂量下具有<300nm 的空间分辨率,并且由于 MONP 的二次离子产率高,没有离子束损伤,这可以提供几种蛋白质的同时成像,特别是来自细胞膜的蛋白质。我们将我们的新成像技术应用于来自对照和阿尔茨海默病(AD)模型小鼠的海马组织样本的研究;海马 CA1 区蛋白簇的接近程度表现出对衰老和 AD 进展的有趣依赖性,这表明蛋白簇的接近程度可能有助于理解微观细胞水平的病理途径。

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