Purification of infection-associated macropinosomes by magnetic isolation for proteomic characterization

Virginie Stévenin, Quentin Giai Gianetto, Magalie Duchateau, Mariette Matondo, Jost Enninga, Yuen-Yan Chang

Published: 2021-10-24 DOI: 10.1038/s41596-021-00610-5

macropinosomes

magnetic isolation

proteomic characterization

bacterial invasion

endocytic vesicles

AI 解读

Fabrication of angstrom-scale two-dimensional channels for mass transport

Efficient and strand-specific profiling of replicating chromatin with enrichment and sequencing of protein-associated nascent DNA in mammalian cells

The eINTACT method for studying nuclear changes in host plant cells targeted by bacterial effectors in native infection contexts

Rapid reaction optimization by robust and economical quantitative benchtop19F NMR spectroscopy

Profiling native pulmonary basement membrane stiffness using atomic force microscopy

Photoimmunotechnology as a powerful biological tool for molecular-based elimination of target cells and microbes, including bacteria, fungi and viruses

Measuring key human carbohydrate digestive enzyme activities using high-performance anion-exchange chromatography with pulsed amperometric detection

Neural cell isolation from adult macaques for high-throughput analyses and neurosphere cultures

Preparation, validation and use of a vasoactive tryptophan-derived hydroperoxide and relevant control compounds

Neuronal subtype-specific growth cone and soma purification from mammalian CNS via fractionation and fluorescent sorting for subcellular analyses and spatial mapping of local transcriptomes and proteomes

查看全部

Sections

Figures

References

Macropinocytosis refers to the nonselective uptake of extracellular molecules into many different types of eukaryotic cells within large fluid-filled vesicles named macropinosomes. Macropinosomes are relevant for a wide variety of cellular processes, such
Introduction
Materials
Procedure
Troubleshooting
Timing
Anticipated results
- Reporting Summary
- References
References
ACKNOWLEDGMENTS

Ha, K. D., Bidlingmaier, S. M. & Liu, B. Macropinocytosis exploitation by cancers and cancer therapeutics. Front. Physiol. 7, 381–381 (2016).
Kumari, S., Mg, S. & Mayor, S. Endocytosis unplugged: multiple ways to enter the cell. Cell Res. 20, 256–275 (2010).
Naslavsky, N. & Caplan, S. The enigmatic endosome—sorting the ins and outs of endocytic trafficking. J. Cell Sci. 131, jcs216499 (2018).
Garcia-Castillo, M. D., Chinnapen, D. J. & Lencer, W. I. Membrane transport across polarized epithelia. Cold Spring Harb. Perspect. Biol. 9 (2017).
Joel, A. S. & Jason, S. K. The breadth of macropinocytosis research. Philos. Trans. R. Soc. Lond. B Biol. Sci. 374, 20180146 (2019).
Lewis, W. H. Pinocytosis by malignant cells. Am. J. Cancer Res. 29, 666–679 (1937).
Egami, Y., Taguchi, T., Maekawa, M., Arai, H. & Araki, N. Small GTPases and phosphoinositides in the regulatory mechanisms of macropinosome formation and maturation. Front. Physiol. 5, 374 (2014).
Kühn, S., Lopez-Montero, N., Chang, Y. Y., Sartori-Rupp, A. & Enninga, J. Imaging macropinosomes during Shigella infections. Methods 127, 12–22 (2017).
Jayashankar, V. & Edinger, A. L. Macropinocytosis confers resistance to therapies targeting cancer anabolism. Nat. Commun. 11, 1121 (2020).
Redelman-Sidi, G. et al. The canonical Wnt pathway drives macropinocytosis in cancer. Cancer Res. 78, 4658–4670 (2018).
Li, Y. et al. Macropinocytosis-mediated membrane recycling drives neural crest migration by delivering F-actin to the lamellipodium. Proc. Natl Acad. Sci. USA 117, 27400 (2020).
Freeman, S. A. et al. Lipid-gated monovalent ion fluxes regulate endocytic traffic and support immune surveillance. Science 367, 301–305 (2020).
Palm, W. Metabolic functions of macropinocytosis. Philos. Trans. R Soc. Lond. B Biol. Sci. 374, 20180285–20180285 (2019).
Canton, J. Macropinocytosis: new insights into its underappreciated role in innate immune cell surveillance. Front. Immunol. 9 (2018).
Liu, Z. & Roche, P. A. Macropinocytosis in phagocytes: regulation of MHC class-II-restricted antigen presentation in dendritic cells. Front. Physiol. 6, 1 (2015).
Kerr, M. C. & Teasdale, R. D. Defining macropinocytosis. Traffic 10, 364–371 (2009).
Jones, A. T., Gumbleton, M. & Duncan, R. Understanding endocytic pathways and intracellular trafficking: a prerequisite for effective design of advanced drug delivery systems. Adv. Drug Deliv. Rev. 55, 1353–1357 (2003).
Buckley, C. M. & King, J. S. Drinking problems: mechanisms of macropinosome formation and maturation. FEBS J. 284, 3778–3790 (2017).
Joel, A. S. & Sei, Y. Macropinosomes as units of signal transduction. Philos. Trans. R. Soc. Lond. BBiol. Sci. 374, 20180157 (2019).
Ford, C., Nans, A., Boucrot, E. & Hayward, R. D. Chlamydia exploits filopodial capture and a macropinocytosis-like pathway for host cell entry. PLoS Pathog. 14, e1007051 (2018).
Lee, C. H. R., Mohamed Hussain, K. & Chu, J. J. H. Macropinocytosis dependent entry of Chikungunya virus into human muscle cells. PLoS Negl. Trop. Dis. 13, e0007610 (2019).
Kälin, S. et al. Macropinocytotic uptake and infection of human epithelial cells with species B2 adenovirus type 35. J. Virol. 84, 5336–5350 (2010).
Torriani, G. et al. Macropinocytosis contributes to hantavirus entry into human airway epithelial cells. Virology 531, 57–68 (2019).
Helenius, A. Virus entry: looking back and moving forward. J. Mol. Biol. 430, 1853–1862 (2018).
Mercer, J. & Helenius, A. Virus entry by macropinocytosis. Nat. Cell Biol. 11, 510–520 (2009).
Hetzenecker, S., Helenius, A. & Krzyzaniak, M. A. HCMV induces macropinocytosis for host cell entry in fibroblasts. Traffic 17, 351–368 (2016).
Garcia-del Portillo, F. & Finlay, B. B. Salmonella invasion of nonphagocytic cells induces formation of macropinosomes in the host cell. Infect. Immun. 62, 4641–4645 (1994).
Weiner, A. et al. Macropinosomes are key players in early Shigella invasion and vacuolar escape in epithelial cells. PLoS Pathog. 12, e1005602 (2016).
Fredlund, J. et al. The entry of Salmonella in a distinct tight compartment revealed at high temporal and ultrastructural resolution. Cell. Microbiol. 20 (2018).
Stévenin, V. et al. Dynamic growth and shrinkage of the Salmonella-containing vacuole determines the intracellular pathogen niche. Cell Rep 29, 3958–3973.e3957 (2019).
Chang, Y.-Y., Enninga, J. & Stévenin, V. New methods to decrypt emerging macropinosome functions during the host–pathogen crosstalk. Cell. Microbiol. 23, e13342 (2021).
Chang, Y.-Y. et al. Shigella hijacks the exocyst to cluster macropinosomes for efficient vacuolar escape. PLoS Pathog 16, e1008822 (2020).
de Araújo, M. E. G., Lamberti, G. & Huber, L. A. Isolation of early and late endosomes by density gradient centrifugation. Cold Spring Habor Protoc. 2015, pdb.prot083444 (2015).
Kobayashi, T. et al. Separation and characterization of late endosomal membrane domains. J. Biol. Chem. 277, 32157–32164 (2002).
Tjelle, T. E., Brech, A., Juvet, L. K., Griffiths, G. & Berg, T. Isolation and characterization of early endosomes, late endosomes and terminal lysosomes: their role in protein degradation. J. Cell Sci. 109, 2905–2914 (1996).
Walker, L. R., Hussein, H. A. & Akula, S. M. Subcellular fractionation method to study endosomal trafficking of Kaposi’s sarcoma-associated herpesvirus. Cell Biosci. 6, 1 (2016).
Plouffe, B. D., Murthy, S. K. & Lewis, L. H. Fundamentals and application of magnetic particles in cell isolation and enrichment: a review. Rep. Prog. Phys. 78, 016601–016601 (2015).
Wittrup, A. et al. Magnetic nanoparticle-based isolation of endocytic vesicles reveals a role of the heat shock protein GRP75 in macromolecular delivery. Proc. Natl Acad. Sci. USA 107, 13342–13347 (2010).
Miltenyi, S., Muller, W., Weichel, W. & Radbruch, A. High gradient magnetic cell separation with MACS. Cytometry 11, 231–238 (1990).
Özbaykal, G. et al. The transpeptidase PBP2 governs initial localization and activity of the major cell-wall synthesis machinery in E. coli. eLife 9, e50629 (2020).
Vigouroux, A. et al. Class-A penicillin binding proteins do not contribute to cell shape but repair cell-wall defects. eLife 9, e51998 (2020).
Haigler, H. T., McKanna, J. A. & Cohen, S. Rapid stimulation of pinocytosis in human carcinoma cells A-431 by epidermal growth factor. J. Cell Biol. 83, 82–90 (1979).
Fujii, M., Kawai, K., Egami, Y. & Araki, N. Dissecting the roles of Rac1 activation and deactivation in macropinocytosis using microscopic photo-manipulation. Sci. Rep. 3, 2385 (2013).
Nakase, I. et al. Cellular uptake of arginine-rich peptides: roles for macropinocytosis and actin rearrangement. Mol. Ther. 10, 1011–1022 (2004).
Al-Taei, S. et al. Intracellular traffic and fate of protein transduction domains HIV-1 TAT peptide and octaarginine. implications for their utilization as drug delivery vectors. Bioconjug. Chem. 17, 90–100 (2006).
Nakase, I. et al. Interaction of arginine-rich peptides with membrane-associated proteoglycans is crucial for induction of actin organization and macropinocytosis. Biochemistry 46, 492–501 (2007).
D’Astolfo, D. S. et al. Efficient intracellular delivery of native proteins. Cell 161, 674–690 (2015).
Hetrick, B. et al. Small molecules CK-666 and CK-869 inhibit actin-related protein 2/3 complex by blocking an activating conformational change. Chem. Biol. 20, 701–712 (2013).
Koivusalo, M. et al. Amiloride inhibits macropinocytosis by lowering submembranous pH and preventing Rac1 and Cdc42 signaling. J. Cell Biol. 188, 547–563 (2010).
Ivanov, A.I. Pharmacological inhibition of endocytic pathways: is it specific enough to be useful? in Exocytosis and Endocytosis (ed. Ivanov, A. I.) 15–33 (Humana Press, 2008).
Addi, C. et al. The Flemmingsome reveals an ESCRT-to-membrane coupling via ALIX/syntenin/syndecan-4 required for completion of cytokinesis. Nat. Commun. 11, 1941 (2020).
Rizzo, J. et al. Characterization of extracellular vesicles produced by Aspergillus fumigatus protoplasts. mSphere 5, e00476–00420 (2020).
Lelouard, H. et al. Pathogenic bacteria and dead cells are internalized by a unique subset of Peyer’s patch dendritic cells that express lysozyme. Gastroenterology 138, 173–184.e171-173 (2010).
Tyanova, S., Temu, T. & Cox, J. The MaxQuant computational platform for mass spectrometry-based shotgun proteomics. Nat. Protoc. 11, 2301–2319 (2016).
Cox, J. & Mann, M. MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification. Nat. Biotechnol. 26, 1367–1372 (2008).
Wieczorek, S. et al. DAPAR & ProStaR: software to perform statistical analyses in quantitative discovery proteomics. Bioinformatics 33, 135–136 (2017).
Giai Gianetto, Q., Wieczorek, S., Couté, Y. & Burger, T. A peptide-level multiple imputation strategy accounting for the different natures of missing values in proteomics data. Preprint at bioRxiv https://doi.org/10.1101/2020.05.29.122770 (2020).
Giai Gianetto, Q. et al. Calibration plot for proteomics: a graphical tool to visually check the assumptions underlying FDR control in quantitative experiments. Proteomics 16, 29–32 (2016).
Ritchie, M. E. et al. limma powers differential expression analyses for RNA-sequencing and microarray studies. Nucleic Acids Res. 43, e47 (2015).
Mi, H., Muruganujan, A., Ebert, D., Huang, X. & Thomas, P. D. PANTHER version 14: more genomes, a new PANTHER GO-slim and improvements in enrichment analysis tools. Nucleic Acids Res. 47, D419–D426 (2018).
Santos, J. C. et al. The COPII complex and lysosomal VAMP7 determine intracellular Salmonella localization and growth. Cell. Microbiol. 17, 1699–1720 (2015).
Ibarra, J. A. et al. Induction of Salmonella pathogenicity island 1 under different growth conditions can affect Salmonella-host cell interactions in vitro. Microbiology 156, 1120–1133 (2010).
Steele-Mortimer, O. Infection of epithelial cells with Salmonella enterica. in Bacterial Pathogenesis: Methods and Protocols (eds. DeLeo, F. R. & Otto, M.) 201–211 (Humana Press, 2008).
Li, L. et al. The effect of the size of fluorescent dextran on its endocytic pathway. Cell Biol. Int. 39, 531–539 (2015).

Purification of infection-associated macropinosomes by magnetic isolation for proteomic characterization

Supplementary information

推荐阅读