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相关的三维冷冻X射线成像揭示了设计的抗纤维化蛋白质-纳米材料杂化物的细胞内定位及其作用。

Correlative 3D cryo X-ray imaging reveals intracellular location and effect of designed antifibrotic protein-nanomaterial hybrids.

作者信息

Groen J, Palanca A, Aires A, Conesa J J, Maestro D, Rehbein S, Harkiolaki M, Villar A V, Cortajarena A L, Pereiro E

机构信息

MISTRAL Beamline, Experiments Division, ALBA Synchrotron Light Source Cerdanyola del Valles 08290 Barcelona Spain

Instituto de Biomedicina y Biotecnologia de Cantabria (IBBTEC), University of Cantabria, CSIC 39011 Santander Spain.

出版信息

Chem Sci. 2021 Oct 19;12(45):15090-15103. doi: 10.1039/d1sc04183e. eCollection 2021 Nov 24.

DOI:10.1039/d1sc04183e
PMID:34909150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8612387/
Abstract

Revealing the intracellular location of novel therapeutic agents is paramount for the understanding of their effect at the cell ultrastructure level. Here, we apply a novel correlative cryo 3D imaging approach to determine the intracellular fate of a designed protein-nanomaterial hybrid with antifibrotic properties that shows great promise in mitigating myocardial fibrosis. Cryo 3D structured illumination microscopy (cryo-3D-SIM) pinpoints the location and cryo soft X-ray tomography (cryo-SXT) reveals the ultrastructural environment and subcellular localization of this nanomaterial with spatial correlation accuracy down to 70 nm in whole cells. This novel high resolution 3D cryo correlative approach unambiguously locates the nanomaterial after overnight treatment within multivesicular bodies which have been associated with endosomal trafficking events by confocal microscopy. Moreover, this approach allows assessing the cellular response towards the treatment by evaluating the morphological changes induced. This is especially relevant for the future usage of nanoformulations in clinical practices. This correlative super-resolution and X-ray imaging strategy joins high specificity, by the use of fluorescence, with high spatial resolution at 30 nm (half pitch) provided by cryo-SXT in whole cells, without the need of staining or fixation, and can be of particular benefit to locate specific molecules in the native cellular environment in bio-nanomedicine.

摘要

揭示新型治疗剂的细胞内定位对于在细胞超微结构水平上理解其作用至关重要。在此,我们应用一种新型的相关冷冻三维成像方法来确定一种具有抗纤维化特性的设计蛋白质-纳米材料杂化物的细胞内命运,该杂化物在减轻心肌纤维化方面显示出巨大潜力。冷冻三维结构照明显微镜(cryo-3D-SIM)可精确定位其位置,而冷冻软X射线断层扫描(cryo-SXT)则揭示该纳米材料的超微结构环境和亚细胞定位,在全细胞中的空间相关精度可达70纳米。这种新型的高分辨率三维冷冻相关方法明确地将纳米材料定位在过夜处理后的多囊泡体内,通过共聚焦显微镜观察发现这些多囊泡体与内体运输事件有关。此外,这种方法能够通过评估诱导的形态变化来评估细胞对治疗的反应。这对于纳米制剂在临床实践中的未来应用尤为重要。这种相关的超分辨率和X射线成像策略结合了荧光的高特异性以及cryo-SXT在全细胞中提供的30纳米(半间距)高空间分辨率,无需染色或固定,在生物纳米医学中对在天然细胞环境中定位特定分子可能特别有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/8a36fce06f2f/d1sc04183e-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/e13fe02e1879/d1sc04183e-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/c47eb034cf23/d1sc04183e-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/b1f2e05c34ed/d1sc04183e-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/2d2a33bf0d59/d1sc04183e-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/8a36fce06f2f/d1sc04183e-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/e13fe02e1879/d1sc04183e-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/c47eb034cf23/d1sc04183e-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/b1f2e05c34ed/d1sc04183e-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/2d2a33bf0d59/d1sc04183e-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/8612387/8a36fce06f2f/d1sc04183e-f5.jpg

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