Automated single-molecule imaging in living cells
An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-mo...
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Published in | Nature communications Vol. 9; no. 1; pp. 3061 - 11 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
03.08.2018
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Abstract | An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-molecule tracking, are fully automated, and numerous highly accurate, efficient, and reproducible single-molecule imaging experiments in living cells can be performed. Here, the apparatus is applied for single-molecule imaging and analysis of epidermal growth factor receptors (EGFRs) in 1600 cells in a 96-well plate within 1 day. Changes in the lateral mobility of EGFRs on the plasma membrane in response to various ligands and drug concentrations are clearly detected in individual cells, and several dynamic and pharmacological parameters are determined, including the diffusion coefficient, oligomer size, and half-maximal effective concentration (EC
50
). Automated single-molecule imaging for systematic cell signaling analyses is feasible and can be applied to single-molecule screening, thus extensively contributing to biological and pharmacological research.
Large scale live cell screens often lack single-molecule resolution. Here the authors present an artificial intelligence-assisted TIRF microscope with automated cell searching and focusing, and use it for high-throughput single-molecule imaging of EGFR dynamics in response to various stimuli. |
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AbstractList | An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-molecule tracking, are fully automated, and numerous highly accurate, efficient, and reproducible single-molecule imaging experiments in living cells can be performed. Here, the apparatus is applied for single-molecule imaging and analysis of epidermal growth factor receptors (EGFRs) in 1600 cells in a 96-well plate within 1 day. Changes in the lateral mobility of EGFRs on the plasma membrane in response to various ligands and drug concentrations are clearly detected in individual cells, and several dynamic and pharmacological parameters are determined, including the diffusion coefficient, oligomer size, and half-maximal effective concentration (EC
50
). Automated single-molecule imaging for systematic cell signaling analyses is feasible and can be applied to single-molecule screening, thus extensively contributing to biological and pharmacological research. An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-molecule tracking, are fully automated, and numerous highly accurate, efficient, and reproducible single-molecule imaging experiments in living cells can be performed. Here, the apparatus is applied for single-molecule imaging and analysis of epidermal growth factor receptors (EGFRs) in 1600 cells in a 96-well plate within 1 day. Changes in the lateral mobility of EGFRs on the plasma membrane in response to various ligands and drug concentrations are clearly detected in individual cells, and several dynamic and pharmacological parameters are determined, including the diffusion coefficient, oligomer size, and half-maximal effective concentration (EC 50 ). Automated single-molecule imaging for systematic cell signaling analyses is feasible and can be applied to single-molecule screening, thus extensively contributing to biological and pharmacological research. Large scale live cell screens often lack single-molecule resolution. Here the authors present an artificial intelligence-assisted TIRF microscope with automated cell searching and focusing, and use it for high-throughput single-molecule imaging of EGFR dynamics in response to various stimuli. An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-molecule tracking, are fully automated, and numerous highly accurate, efficient, and reproducible single-molecule imaging experiments in living cells can be performed. Here, the apparatus is applied for single-molecule imaging and analysis of epidermal growth factor receptors (EGFRs) in 1600 cells in a 96-well plate within 1 day. Changes in the lateral mobility of EGFRs on the plasma membrane in response to various ligands and drug concentrations are clearly detected in individual cells, and several dynamic and pharmacological parameters are determined, including the diffusion coefficient, oligomer size, and half-maximal effective concentration (EC ). Automated single-molecule imaging for systematic cell signaling analyses is feasible and can be applied to single-molecule screening, thus extensively contributing to biological and pharmacological research. Large scale live cell screens often lack single-molecule resolution. Here the authors present an artificial intelligence-assisted TIRF microscope with automated cell searching and focusing, and use it for high-throughput single-molecule imaging of EGFR dynamics in response to various stimuli. An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-molecule tracking, are fully automated, and numerous highly accurate, efficient, and reproducible single-molecule imaging experiments in living cells can be performed. Here, the apparatus is applied for single-molecule imaging and analysis of epidermal growth factor receptors (EGFRs) in 1600 cells in a 96-well plate within 1 day. Changes in the lateral mobility of EGFRs on the plasma membrane in response to various ligands and drug concentrations are clearly detected in individual cells, and several dynamic and pharmacological parameters are determined, including the diffusion coefficient, oligomer size, and half-maximal effective concentration (EC50). Automated single-molecule imaging for systematic cell signaling analyses is feasible and can be applied to single-molecule screening, thus extensively contributing to biological and pharmacological research. An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-molecule tracking, are fully automated, and numerous highly accurate, efficient, and reproducible single-molecule imaging experiments in living cells can be performed. Here, the apparatus is applied for single-molecule imaging and analysis of epidermal growth factor receptors (EGFRs) in 1600 cells in a 96-well plate within 1 day. Changes in the lateral mobility of EGFRs on the plasma membrane in response to various ligands and drug concentrations are clearly detected in individual cells, and several dynamic and pharmacological parameters are determined, including the diffusion coefficient, oligomer size, and half-maximal effective concentration (EC50). Automated single-molecule imaging for systematic cell signaling analyses is feasible and can be applied to single-molecule screening, thus extensively contributing to biological and pharmacological research.An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant procedures, i.e., searching for cells suitable for observation, detecting in-focus positions, and performing image acquisition and single-molecule tracking, are fully automated, and numerous highly accurate, efficient, and reproducible single-molecule imaging experiments in living cells can be performed. Here, the apparatus is applied for single-molecule imaging and analysis of epidermal growth factor receptors (EGFRs) in 1600 cells in a 96-well plate within 1 day. Changes in the lateral mobility of EGFRs on the plasma membrane in response to various ligands and drug concentrations are clearly detected in individual cells, and several dynamic and pharmacological parameters are determined, including the diffusion coefficient, oligomer size, and half-maximal effective concentration (EC50). Automated single-molecule imaging for systematic cell signaling analyses is feasible and can be applied to single-molecule screening, thus extensively contributing to biological and pharmacological research. |
ArticleNumber | 3061 |
Author | Yasui, Masato Kozuka, Jun Sako, Yasushi Ueda, Masahiro Hiroshima, Michio |
Author_xml | – sequence: 1 givenname: Masato surname: Yasui fullname: Yasui, Masato organization: Laboratory for Cell Signaling Dynamics, RIKEN BDR – sequence: 2 givenname: Michio surname: Hiroshima fullname: Hiroshima, Michio organization: Laboratory for Cell Signaling Dynamics, RIKEN BDR, Cellular Informatics Laboratory, RIKEN – sequence: 3 givenname: Jun surname: Kozuka fullname: Kozuka, Jun organization: Laboratory for Cell Signaling Dynamics, RIKEN BDR – sequence: 4 givenname: Yasushi surname: Sako fullname: Sako, Yasushi email: sako@riken.jp organization: Cellular Informatics Laboratory, RIKEN – sequence: 5 givenname: Masahiro surname: Ueda fullname: Ueda, Masahiro email: masahiroueda@riken.jp organization: Laboratory for Cell Signaling Dynamics, RIKEN BDR, Laboratory of Single Molecule Biology, Graduate School of Frontier Biosciences, Osaka University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30076305$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1158/1078-0432.CCR-05-1554 10.1038/nsmb.2135 10.1006/bbrc.1997.6732 10.1016/S0021-9258(18)67114-5 10.1126/science.1188308 10.1109/TAC.1974.1100705 10.1016/j.cell.2010.06.011 10.1371/journal.pcbi.1003817 10.1098/rsos.160225 10.1038/nrm1962 10.7554/eLife.11835 10.1038/sj.onc.1205028 10.1038/nrc1360 10.1371/journal.pcbi.1002862 10.1242/jcs.02300 10.1038/35004044 10.1021/jp710302j 10.1038/nmeth.2808 10.1090/qam/10666 10.1073/pnas.1200464109 10.1016/0092-8674(92)90167-B 10.1090/S0025-5718-1980-0572855-7 10.1016/j.bbamem.2012.08.022 10.1016/j.bbrc.2008.02.084 10.1109/ICCV.2015.178 10.1145/1830483.1830503 10.1002/chem.200902963 10.1016/j.jmb.2018.02.018 10.1126/science.1063951 10.1074/jbc.273.52.35000 10.1152/physrev.00030.2015 10.1109/TSMC.1979.4310076 10.1016/j.bpj.2009.06.007 10.1038/374555a0 10.1038/ncomms13307 |
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References | HiroshimaMTransient acceleration of epidermal growth factor receptor dynamics produces higher-order signaling clustersJ. Mol. Biol.20184301386140110.1016/j.jmb.2018.02.018295057561:CAS:528:DC%2BC1cXjvFygtLo%3D Kingma, D. P. & Ba, J. Adam: a method for stochastic optimization. In 3rd Int. Conf. Learn. Represent. 1–15 (2014). https://doi.org/10.1145/1830483.1830503 CarterRESorkinAEndocytosis of functional epidermal growth factor receptor-green fluorescent protein chimeraJ. Biol. Chem.1998273350003500710.1074/jbc.273.52.3500098570321:CAS:528:DyaK1MXisFajtA%3D%3D TokunagaMKitamuraKSaitoKIwaneAHYanagidaTSingle molecule imaging of fluorophores and enzymatic reactions achieved by objective-type total internal reflection fluorescence microscopyBiochem. Biophys. Res. Commun.1997235475310.1006/bbrc.1997.673291960331:CAS:528:DyaK2sXjvFSksLc%3D BoggaraMAthmakuriKSrivastavaSColeRKaneRSCharacterization of the diffusion of epidermal growth factor receptor clusters by single particle trackingBiochim. Biophys. Acta2013182841942610.1016/j.bbamem.2012.08.022229748161:CAS:528:DC%2BC3sXhtVOhsQ%3D%3D TaniguchiYQuantifying E. coli proteome and transcriptome with single-molecule sensitivity in single cellsScience20103295335382010Sci...329..533T10.1126/science.11883082067118229229151:CAS:528:DC%2BC3cXptlCltbo%3D JadwinJATime-resolved multimodal analysis of src homology 2 (SH2) domain binding in signaling by receptor tyrosine kinaseseLife2016512610.7554/eLife.11835 ChenouardNObjective comparison of particle tracking methodsNat. Methods20141128128910.1038/nmeth.28082444193641317361:CAS:528:DC%2BC2cXps1GisQ%3D%3D LemmonMASchlessingerJCell signaling by receptor tyrosine kinasesCell20101411117113410.1016/j.cell.2010.06.0112060299629141051:CAS:528:DC%2BC3cXovFartb0%3D MatsuokaSShibataTUedaMAsymmetric PTEN distribution regulated by spatial heterogeneity in membrane-binding state transitionsPLoS Comput. Biol.20139e10028622013PLSCB...9E2862M10.1371/journal.pcbi.10028622332622435420791:CAS:528:DC%2BC3sXivVehsrc%3D UedaMSakoYTanakaTDevreotesPYanagidaTSingle-molecule analysis of chemotactic signaling in Dictyostelium cellsScience20012948648672001Sci...294..864U10.1126/science.1063951116796731:CAS:528:DC%2BD3MXotVCgsrw%3D ScaltritiMBaselgaJThe epidermal growth factor receptor pathway : a model for targeted therapyClin. Cancer Res.2006125268527210.1158/1078-0432.CCR-05-1554170006581:CAS:528:DC%2BD28XpvFShs74%3D KawashimaNReversible dimerization of EGFR revealed by single-molecule fluorescence imaging using quantum dotsChemistry2010161186119210.1002/chem.200902963200249991:CAS:528:DC%2BC3cXhtVKitbc%3D LommersePHMSnaar-JagalskaBESpainkHPSchmidtTSingle-molecule diffusion measurements of H-Ras at the plasma membrane of live cells reveal microdomain localization upon activationJ. Cell Sci.20051181799180910.1242/jcs.02300158607281:CAS:528:DC%2BD2MXkslOgur4%3D NocedalJUpdating quasi-Newton matrices with limited storageMath. Comput.19803577377357285510.1090/S0025-5718-1980-0572855-70464.65037 WilsonRSAutomated single particle detection and tracking for large microscopy datasetsR. Soc. Open Sci.2016316022510.1098/rsos.1602252729380148924631:CAS:528:DC%2BC2sXjt1OkurY%3D OtsuNA threshold selection method from Gray-level histogramsIEEE. Trans. Syst. Man. Cybern.19799626610.1109/TSMC.1979.4310076 CitriAYardenYEGF-ERBB signalling: towards the systems levelNat. Rev. Mol. Cell Biol.2006750551610.1038/nrm1962168299811:CAS:528:DC%2BD28Xms1OhsLc%3D LevenbergKA method for the solution of certain non-linear problems in leastQ. Appl. Math.194421641681066610.1090/qam/106660063.03501 LowensteinEJThe SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signalingCell19927043144210.1016/0092-8674(92)90167-B13227981:CAS:528:DyaK3sXkt1ajtbg%3D Funatsu, T., Harada, Y., Tokunaga, M., Saito, K. & Yanagida, T. Imaging of single fluorescent molecules and individual ATP turnovers by single myosin molecules in aqueous solution. Nature374, 555–559 (1995). LasdonLSFoxRLRatnerMWNonlinear optimization using the generalized reduced gradient methodRev. Fr. D’Automatique, Inform., Rech. Opérationnelle19743731044517130329.90060 XiaoZZhangWYangYXuLFangXSingle-molecule diffusion study of activated EGFR implicates its endocytic pathwayBiochem. Biophys. Res. Commun.200836973073410.1016/j.bbrc.2008.02.084183133981:CAS:528:DC%2BD1cXjs12ns70%3D MatsuokaSShibataTUedaMStatistical analysis of lateral diffusion and multistate kinetics in single-molecule imagingBiophys. J.200997111511242009BpJ....97.1115M10.1016/j.bpj.2009.06.0071968665927263281:CAS:528:DC%2BD1MXhtFOgsL3L GschwindAFischerOMUllrichAThe discovery of receptor tyrosine kinases: targets for cancer therapyNat. Rev. Cancer2004436137010.1038/nrc1360151222071:CAS:528:DC%2BD2cXjsFSlu7g%3D HiroshimaMSaekiYOkada-HatakeyamaMSakoYDynamically varying interactions between heregulin and ErbB proteins detected by single-molecule analysis in living cellsProc. Natl Acad. Sci. USA201210913984139892012PNAS..10913984H10.1073/pnas.120046410922891299 SakoYMinoghchiSYanagidaTSingle-molecule imaging of EGFR signalling on the surface of living cellsNat. Cell Biol.2000216817210.1038/35004044107070881:CAS:528:DC%2BD3cXhvVGnt7w%3D LivnehEReconstitution of human epidermal growth factor receptors and its deletion mutants in cultured hamster cellsJ. Biol. Chem.1986261124901249730179771:CAS:528:DyaL28XlvVCit70%3D YasuiMMatsuokaSUedaMPTEN hopping on the cell membrane is regulated via a positively-charged C2 domainPLoS Comput. Biol.201410e10038172014PLSCB..10E3817Y10.1371/journal.pcbi.10038172521120641612991:CAS:528:DC%2BC2cXhslShsbrK ChenJExpression and function of the epidermal growth factor receptor in physiology and diseasePhysiol. Rev.201696102510692016ippc.book.....C10.1152/physrev.00030.20151:CAS:528:DC%2BC1cXkvFert78%3D NeedhamSREGFR oligomerization organizes kinase-active dimers into competent signalling platformsNat. Commun.201672016NatCo...713307N10.1038/ncomms133072779630850955841:CAS:528:DC%2BC28XhvVSisLfJ Low-NamSTErbB1 dimerization is promoted by domain co-confinement and stabilized by ligand bindingNat. Struct. Mol. Biol.2011181244124910.1038/nsmb.21352202029932103211:CAS:528:DC%2BC3MXhtlGks7vJ BishopPCDiferential sensitivity of cancer cells to inhibitors of the epidermal growth factor receptor familyOncogene20022111912710.1038/sj.onc.1205028117911821:CAS:528:DC%2BD38Xos1yiug%3D%3D XiaoZSingle-molecule study of lateral mobility of epidermal growth factor receptor 2/HER2 on activationJ. Phys. Chem. B20081124140414510.1021/jp710302j183248051:CAS:528:DC%2BD1cXivV2gur4%3D Noh, H., Hong, S. & Han, B. Learning deconvolution network for semantic segmentation. In Proc. IEEE Int. Conf. Comput. Vis. 7–13 December, 1520–1528 (IEEE Computer Society Washington, DC, 2015). AkaikeHA new look at the statistical model identificationIEEE Trans. Autom. Contr.1974197167231974ITAC...19..716A42371610.1109/TAC.1974.11007050314.62039 M Boggara (5524_CR13) 2013; 1828 K Levenberg (5524_CR36) 1944; 2 A Citri (5524_CR9) 2006; 7 PC Bishop (5524_CR20) 2002; 21 ST Low-Nam (5524_CR14) 2011; 18 M Hiroshima (5524_CR17) 2018; 430 M Yasui (5524_CR26) 2014; 10 M Tokunaga (5524_CR6) 1997; 235 EJ Lowenstein (5524_CR22) 1992; 70 N Otsu (5524_CR29) 1979; 9 J Nocedal (5524_CR34) 1980; 35 RE Carter (5524_CR5) 1998; 273 Y Sako (5524_CR2) 2000; 2 Z Xiao (5524_CR15) 2008; 369 Y Taniguchi (5524_CR4) 2010; 329 MA Lemmon (5524_CR8) 2010; 141 N Kawashima (5524_CR16) 2010; 16 PHM Lommerse (5524_CR32) 2005; 118 Z Xiao (5524_CR18) 2008; 112 N Chenouard (5524_CR31) 2014; 11 S Matsuoka (5524_CR24) 2009; 97 5524_CR28 5524_CR1 5524_CR7 J Chen (5524_CR11) 2016; 96 E Livneh (5524_CR21) 1986; 261 JA Jadwin (5524_CR23) 2016; 5 A Gschwind (5524_CR12) 2004; 4 SR Needham (5524_CR27) 2016; 7 H Akaike (5524_CR33) 1974; 19 M Hiroshima (5524_CR19) 2012; 109 RS Wilson (5524_CR30) 2016; 3 M Ueda (5524_CR3) 2001; 294 M Scaltriti (5524_CR10) 2006; 12 S Matsuoka (5524_CR25) 2013; 9 LS Lasdon (5524_CR35) 1974; 3 |
References_xml | – reference: KawashimaNReversible dimerization of EGFR revealed by single-molecule fluorescence imaging using quantum dotsChemistry2010161186119210.1002/chem.200902963200249991:CAS:528:DC%2BC3cXhtVKitbc%3D – reference: TokunagaMKitamuraKSaitoKIwaneAHYanagidaTSingle molecule imaging of fluorophores and enzymatic reactions achieved by objective-type total internal reflection fluorescence microscopyBiochem. Biophys. Res. Commun.1997235475310.1006/bbrc.1997.673291960331:CAS:528:DyaK2sXjvFSksLc%3D – reference: CarterRESorkinAEndocytosis of functional epidermal growth factor receptor-green fluorescent protein chimeraJ. Biol. Chem.1998273350003500710.1074/jbc.273.52.3500098570321:CAS:528:DyaK1MXisFajtA%3D%3D – reference: ChenJExpression and function of the epidermal growth factor receptor in physiology and diseasePhysiol. Rev.201696102510692016ippc.book.....C10.1152/physrev.00030.20151:CAS:528:DC%2BC1cXkvFert78%3D – reference: YasuiMMatsuokaSUedaMPTEN hopping on the cell membrane is regulated via a positively-charged C2 domainPLoS Comput. Biol.201410e10038172014PLSCB..10E3817Y10.1371/journal.pcbi.10038172521120641612991:CAS:528:DC%2BC2cXhslShsbrK – reference: HiroshimaMSaekiYOkada-HatakeyamaMSakoYDynamically varying interactions between heregulin and ErbB proteins detected by single-molecule analysis in living cellsProc. Natl Acad. Sci. USA201210913984139892012PNAS..10913984H10.1073/pnas.120046410922891299 – reference: UedaMSakoYTanakaTDevreotesPYanagidaTSingle-molecule analysis of chemotactic signaling in Dictyostelium cellsScience20012948648672001Sci...294..864U10.1126/science.1063951116796731:CAS:528:DC%2BD3MXotVCgsrw%3D – reference: LommersePHMSnaar-JagalskaBESpainkHPSchmidtTSingle-molecule diffusion measurements of H-Ras at the plasma membrane of live cells reveal microdomain localization upon activationJ. Cell Sci.20051181799180910.1242/jcs.02300158607281:CAS:528:DC%2BD2MXkslOgur4%3D – reference: WilsonRSAutomated single particle detection and tracking for large microscopy datasetsR. Soc. Open Sci.2016316022510.1098/rsos.1602252729380148924631:CAS:528:DC%2BC2sXjt1OkurY%3D – reference: Funatsu, T., Harada, Y., Tokunaga, M., Saito, K. & Yanagida, T. Imaging of single fluorescent molecules and individual ATP turnovers by single myosin molecules in aqueous solution. Nature374, 555–559 (1995). – reference: LivnehEReconstitution of human epidermal growth factor receptors and its deletion mutants in cultured hamster cellsJ. Biol. Chem.1986261124901249730179771:CAS:528:DyaL28XlvVCit70%3D – reference: HiroshimaMTransient acceleration of epidermal growth factor receptor dynamics produces higher-order signaling clustersJ. Mol. Biol.20184301386140110.1016/j.jmb.2018.02.018295057561:CAS:528:DC%2BC1cXjvFygtLo%3D – reference: MatsuokaSShibataTUedaMStatistical analysis of lateral diffusion and multistate kinetics in single-molecule imagingBiophys. J.200997111511242009BpJ....97.1115M10.1016/j.bpj.2009.06.0071968665927263281:CAS:528:DC%2BD1MXhtFOgsL3L – reference: Low-NamSTErbB1 dimerization is promoted by domain co-confinement and stabilized by ligand bindingNat. Struct. Mol. Biol.2011181244124910.1038/nsmb.21352202029932103211:CAS:528:DC%2BC3MXhtlGks7vJ – reference: MatsuokaSShibataTUedaMAsymmetric PTEN distribution regulated by spatial heterogeneity in membrane-binding state transitionsPLoS Comput. Biol.20139e10028622013PLSCB...9E2862M10.1371/journal.pcbi.10028622332622435420791:CAS:528:DC%2BC3sXivVehsrc%3D – reference: OtsuNA threshold selection method from Gray-level histogramsIEEE. Trans. Syst. Man. Cybern.19799626610.1109/TSMC.1979.4310076 – reference: Kingma, D. P. & Ba, J. Adam: a method for stochastic optimization. In 3rd Int. Conf. Learn. Represent. 1–15 (2014). https://doi.org/10.1145/1830483.1830503 – reference: NeedhamSREGFR oligomerization organizes kinase-active dimers into competent signalling platformsNat. Commun.201672016NatCo...713307N10.1038/ncomms133072779630850955841:CAS:528:DC%2BC28XhvVSisLfJ – reference: GschwindAFischerOMUllrichAThe discovery of receptor tyrosine kinases: targets for cancer therapyNat. Rev. Cancer2004436137010.1038/nrc1360151222071:CAS:528:DC%2BD2cXjsFSlu7g%3D – reference: CitriAYardenYEGF-ERBB signalling: towards the systems levelNat. Rev. Mol. Cell Biol.2006750551610.1038/nrm1962168299811:CAS:528:DC%2BD28Xms1OhsLc%3D – reference: TaniguchiYQuantifying E. coli proteome and transcriptome with single-molecule sensitivity in single cellsScience20103295335382010Sci...329..533T10.1126/science.11883082067118229229151:CAS:528:DC%2BC3cXptlCltbo%3D – reference: ScaltritiMBaselgaJThe epidermal growth factor receptor pathway : a model for targeted therapyClin. Cancer Res.2006125268527210.1158/1078-0432.CCR-05-1554170006581:CAS:528:DC%2BD28XpvFShs74%3D – reference: LowensteinEJThe SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signalingCell19927043144210.1016/0092-8674(92)90167-B13227981:CAS:528:DyaK3sXkt1ajtbg%3D – reference: Noh, H., Hong, S. & Han, B. Learning deconvolution network for semantic segmentation. In Proc. IEEE Int. Conf. Comput. Vis. 7–13 December, 1520–1528 (IEEE Computer Society Washington, DC, 2015). – reference: SakoYMinoghchiSYanagidaTSingle-molecule imaging of EGFR signalling on the surface of living cellsNat. Cell Biol.2000216817210.1038/35004044107070881:CAS:528:DC%2BD3cXhvVGnt7w%3D – reference: JadwinJATime-resolved multimodal analysis of src homology 2 (SH2) domain binding in signaling by receptor tyrosine kinaseseLife2016512610.7554/eLife.11835 – reference: AkaikeHA new look at the statistical model identificationIEEE Trans. Autom. Contr.1974197167231974ITAC...19..716A42371610.1109/TAC.1974.11007050314.62039 – reference: XiaoZZhangWYangYXuLFangXSingle-molecule diffusion study of activated EGFR implicates its endocytic pathwayBiochem. Biophys. Res. Commun.200836973073410.1016/j.bbrc.2008.02.084183133981:CAS:528:DC%2BD1cXjs12ns70%3D – reference: XiaoZSingle-molecule study of lateral mobility of epidermal growth factor receptor 2/HER2 on activationJ. Phys. Chem. B20081124140414510.1021/jp710302j183248051:CAS:528:DC%2BD1cXivV2gur4%3D – reference: LevenbergKA method for the solution of certain non-linear problems in leastQ. Appl. Math.194421641681066610.1090/qam/106660063.03501 – reference: LemmonMASchlessingerJCell signaling by receptor tyrosine kinasesCell20101411117113410.1016/j.cell.2010.06.0112060299629141051:CAS:528:DC%2BC3cXovFartb0%3D – reference: ChenouardNObjective comparison of particle tracking methodsNat. Methods20141128128910.1038/nmeth.28082444193641317361:CAS:528:DC%2BC2cXps1GisQ%3D%3D – reference: BoggaraMAthmakuriKSrivastavaSColeRKaneRSCharacterization of the diffusion of epidermal growth factor receptor clusters by single particle trackingBiochim. Biophys. Acta2013182841942610.1016/j.bbamem.2012.08.022229748161:CAS:528:DC%2BC3sXhtVOhsQ%3D%3D – reference: BishopPCDiferential sensitivity of cancer cells to inhibitors of the epidermal growth factor receptor familyOncogene20022111912710.1038/sj.onc.1205028117911821:CAS:528:DC%2BD38Xos1yiug%3D%3D – reference: NocedalJUpdating quasi-Newton matrices with limited storageMath. Comput.19803577377357285510.1090/S0025-5718-1980-0572855-70464.65037 – reference: LasdonLSFoxRLRatnerMWNonlinear optimization using the generalized reduced gradient methodRev. Fr. D’Automatique, Inform., Rech. Opérationnelle19743731044517130329.90060 – volume: 12 start-page: 5268 year: 2006 ident: 5524_CR10 publication-title: Clin. Cancer Res. doi: 10.1158/1078-0432.CCR-05-1554 – volume: 18 start-page: 1244 year: 2011 ident: 5524_CR14 publication-title: Nat. Struct. Mol. Biol. doi: 10.1038/nsmb.2135 – volume: 235 start-page: 47 year: 1997 ident: 5524_CR6 publication-title: Biochem. Biophys. Res. Commun. doi: 10.1006/bbrc.1997.6732 – volume: 261 start-page: 12490 year: 1986 ident: 5524_CR21 publication-title: J. Biol. Chem. doi: 10.1016/S0021-9258(18)67114-5 – volume: 329 start-page: 533 year: 2010 ident: 5524_CR4 publication-title: Science doi: 10.1126/science.1188308 – volume: 19 start-page: 716 year: 1974 ident: 5524_CR33 publication-title: IEEE Trans. Autom. Contr. doi: 10.1109/TAC.1974.1100705 – volume: 141 start-page: 1117 year: 2010 ident: 5524_CR8 publication-title: Cell doi: 10.1016/j.cell.2010.06.011 – volume: 10 start-page: e1003817 year: 2014 ident: 5524_CR26 publication-title: PLoS Comput. Biol. doi: 10.1371/journal.pcbi.1003817 – volume: 3 start-page: 160225 year: 2016 ident: 5524_CR30 publication-title: R. Soc. Open Sci. doi: 10.1098/rsos.160225 – volume: 7 start-page: 505 year: 2006 ident: 5524_CR9 publication-title: Nat. Rev. Mol. Cell Biol. doi: 10.1038/nrm1962 – volume: 5 start-page: 1 year: 2016 ident: 5524_CR23 publication-title: eLife doi: 10.7554/eLife.11835 – volume: 21 start-page: 119 year: 2002 ident: 5524_CR20 publication-title: Oncogene doi: 10.1038/sj.onc.1205028 – volume: 4 start-page: 361 year: 2004 ident: 5524_CR12 publication-title: Nat. Rev. Cancer doi: 10.1038/nrc1360 – volume: 9 start-page: e1002862 year: 2013 ident: 5524_CR25 publication-title: PLoS Comput. Biol. doi: 10.1371/journal.pcbi.1002862 – volume: 118 start-page: 1799 year: 2005 ident: 5524_CR32 publication-title: J. Cell Sci. doi: 10.1242/jcs.02300 – volume: 2 start-page: 168 year: 2000 ident: 5524_CR2 publication-title: Nat. Cell Biol. doi: 10.1038/35004044 – volume: 112 start-page: 4140 year: 2008 ident: 5524_CR18 publication-title: J. Phys. Chem. B doi: 10.1021/jp710302j – volume: 11 start-page: 281 year: 2014 ident: 5524_CR31 publication-title: Nat. Methods doi: 10.1038/nmeth.2808 – volume: 3 start-page: 73 year: 1974 ident: 5524_CR35 publication-title: Rev. Fr. D’Automatique, Inform., Rech. Opérationnelle – volume: 2 start-page: 164 year: 1944 ident: 5524_CR36 publication-title: Q. Appl. Math. doi: 10.1090/qam/10666 – volume: 109 start-page: 13984 year: 2012 ident: 5524_CR19 publication-title: Proc. Natl Acad. Sci. USA doi: 10.1073/pnas.1200464109 – volume: 70 start-page: 431 year: 1992 ident: 5524_CR22 publication-title: Cell doi: 10.1016/0092-8674(92)90167-B – volume: 35 start-page: 773 year: 1980 ident: 5524_CR34 publication-title: Math. Comput. doi: 10.1090/S0025-5718-1980-0572855-7 – volume: 1828 start-page: 419 year: 2013 ident: 5524_CR13 publication-title: Biochim. Biophys. Acta doi: 10.1016/j.bbamem.2012.08.022 – volume: 369 start-page: 730 year: 2008 ident: 5524_CR15 publication-title: Biochem. Biophys. Res. Commun. doi: 10.1016/j.bbrc.2008.02.084 – ident: 5524_CR7 doi: 10.1109/ICCV.2015.178 – ident: 5524_CR28 doi: 10.1145/1830483.1830503 – volume: 16 start-page: 1186 year: 2010 ident: 5524_CR16 publication-title: Chemistry doi: 10.1002/chem.200902963 – volume: 430 start-page: 1386 year: 2018 ident: 5524_CR17 publication-title: J. Mol. Biol. doi: 10.1016/j.jmb.2018.02.018 – volume: 294 start-page: 864 year: 2001 ident: 5524_CR3 publication-title: Science doi: 10.1126/science.1063951 – volume: 273 start-page: 35000 year: 1998 ident: 5524_CR5 publication-title: J. Biol. Chem. doi: 10.1074/jbc.273.52.35000 – volume: 96 start-page: 1025 year: 2016 ident: 5524_CR11 publication-title: Physiol. Rev. doi: 10.1152/physrev.00030.2015 – volume: 9 start-page: 62 year: 1979 ident: 5524_CR29 publication-title: IEEE. Trans. Syst. Man. Cybern. doi: 10.1109/TSMC.1979.4310076 – volume: 97 start-page: 1115 year: 2009 ident: 5524_CR24 publication-title: Biophys. J. doi: 10.1016/j.bpj.2009.06.007 – ident: 5524_CR1 doi: 10.1038/374555a0 – volume: 7 year: 2016 ident: 5524_CR27 publication-title: Nat. Commun. doi: 10.1038/ncomms13307 |
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Snippet | An automated single-molecule imaging system developed for live-cell analyses based on artificial intelligence-assisted microscopy is presented. All significant... Large scale live cell screens often lack single-molecule resolution. Here the authors present an artificial intelligence-assisted TIRF microscope with... |
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SubjectTerms | 14/56 14/63 631/1647/245/2225 631/57/2265 631/80/86/2368 96/95 Animals Artificial Intelligence Automation Cell Line Cell Membrane Cell Tracking - methods Cells (biology) Cricetulus Diffusion coefficient Dose-Response Relationship, Drug Epidermal growth factor Epidermal growth factor receptors Feasibility studies Fluorescent Dyes Growth factor receptors Growth factors Humanities and Social Sciences Image acquisition Kinetics Models, Biological multidisciplinary Pharmacology Receptors Science Science (multidisciplinary) Single Molecule Imaging - methods |
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Title | Automated single-molecule imaging in living cells |
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