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      Live Intracellular Biorthogonal Imaging by Surface Enhanced Raman Spectroscopy using Alkyne-Silver Nanoparticles Clusters

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          Abstract

          Live intracellular imaging is a valuable tool in modern diagnostics and pharmacology. Surface Enhanced Raman Spectroscopy (SERS) stands out as a non-destructive and multiplexed technique, but intracellular SERS imaging still suffers from interfering background from endogenous components. Here we show the assembly of small colloidal SERS probes with Raman signal in the cell-silent window of 1800–2900 cm −1 for biorthogonal intracellular SERS imaging of dopamine that was undistinguishable from the endogenous cell background. By linking colloidal silver nanoparticles with alkyne-dopamine adducts, clusters are formed by 2–6 nanoparticles spaced by tight interparticle gaps that exhibited high electric field enhancement and strong SERS signals of alkyne and dopamines. Due to the cell-silent signals of the alkyne, intracellular in-vitro Raman imaging shows that the dopamines on the internalized clusters remain distinguishable across the cytoplasm with good spatial resolution. Our method can be a general-purpose method for real-time imaging of biomolecules, such as proteins, peptides, DNA and drugs.

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          Most cited references53

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          Endocytosis and exocytosis of nanoparticles in mammalian cells

          Engineered nanoparticles that can be injected into the human body hold tremendous potential to detect and treat complex diseases. Understanding of the endocytosis and exocytosis mechanisms of nanoparticles is essential for safe and efficient therapeutic application. In particular, exocytosis is of significance in the removal of nanoparticles with drugs and contrast agents from the body, while endocytosis is of great importance for the targeting of nanoparticles in disease sites. Here, we review the recent research on the endocytosis and exocytosis of functionalized nanoparticles based on various sizes, shapes, and surface chemistries. We believe that this review contributes to the design of safe nanoparticles that can efficiently enter and leave human cells and tissues.
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            Size-Dependent Endocytosis of Nanoparticles.

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              Gold nanoparticles induce autophagosome accumulation through size-dependent nanoparticle uptake and lysosome impairment.

              Development of nanotechnology calls for a comprehensive understanding of the impact of nanomaterials on biological systems. Autophagy is a lysosome-based degradative pathway which plays an essential role in maintaining cellular homeostasis. Previous studies have shown that nanoparticles from various sources can induce autophagosome accumulation in treated cells. However, the underlying mechanism is still not clear. Gold nanoparticles (AuNPs) are one of the most widely used nanomaterials and have been reported to induce autophagosome accumulation. In this study, we found that AuNPs can be taken into cells through endocytosis in a size-dependent manner. The internalized AuNPs eventually accumulate in lysosomes and cause impairment of lysosome degradation capacity through alkalinization of lysosomal pH. Consistent with previous studies, we found that AuNP treatment can induce autophagosome accumulation and processing of LC3, an autophagosome marker protein. However, degradation of the autophagy substrate p62 is blocked in AuNP-treated cells, which indicates that autophagosome accumulation results from blockade of autophagy flux, rather than induction of autophagy. Our data clarify the mechanism by which AuNPs induce autophagosome accumulation and reveal the effect of AuNPs on lysosomes. This work is significant to nanoparticle research because it illustrates how nanoparticles can potentially interrupt the autophagic pathway and has important implications for biomedical applications of nanoparticles. © 2011 American Chemical Society
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                Author and article information

                Contributors
                denis.garoli@iit.it
                francesco.deangelis@iit.it
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                23 August 2018
                23 August 2018
                2018
                : 8
                : 12652
                Affiliations
                [1 ]ISNI 0000 0004 1764 2907, GRID grid.25786.3e, Istituto Italiano di Tecnologia, ; Via Morego 30, 16163 Genova, Italy
                [2 ]INCLIVA Instituto de Investigación Sanitaria, Av. Menéndez Pelayo 4, 46010 Valencia, Spain
                [3 ]ISNI 0000 0001 2151 3065, GRID grid.5606.5, University of Genova, ; Via Balbi 5, 16126 Genova, Italy
                [4 ]GRID grid.476002.7, AB ANALITICA s.r.l., ; Via Svizzera 16, 35127 Padova, Italy
                Author information
                http://orcid.org/0000-0002-6564-5972
                http://orcid.org/0000-0002-0143-1510
                Article
                31165
                10.1038/s41598-018-31165-3
                6107644
                30140073
                edc60133-860f-45a8-b5a8-36f6e538dcf6
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 30 May 2018
                : 13 August 2018
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100000781, EC | European Research Council (ERC);
                Award ID: 616213
                Award ID: 616213
                Award ID: 616213
                Award ID: 616213
                Award ID: 616213
                Award ID: 616213
                Award ID: 616213
                Award ID: 616213
                Award ID: 616213
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100007601, EC | Horizon 2020 (European Union Framework Programme for Research and Innovation);
                Award ID: 687089
                Award ID: 687089
                Award ID: 687089
                Award ID: 687089
                Award ID: 687089
                Award ID: 687089
                Award ID: 687089
                Award ID: 687089
                Award ID: 687089
                Award Recipient :
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