Erratum: A Mechanogenetic Toolkit for Interrogating Cell Signaling in Space and Time (Cell (2016) 165(6) (1507–1518)(S0092867416304901)(10.1016/j.cell.2016.04.045));A mechanogenetic toolkit for interrogating cell signaling in space and time

Cell

Volumn 165, Issue 6, 2016, Pages 1507-1518

  Seo, Daeha ^a,b,c   Southard, Kaden M ^a,d   Kim, Ji Wook ^e,f   Lee, Hyun Jung ^a   Farlow, Justin ^d   Lee, Jung Uk ^e,f   Litt, David B ^b,c   Haas, Thomas ^a   Alivisatos, A Paul ^b,c   Cheon, Jinwoo ^e,f   Gartner, Zev J ^d   Jun, Young Wook ^a,d,e,f  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c LAWRENCE BERKELEY NATIONAL LABORATORY   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e Institute for Basic Science   (South Korea)

^f Yonsei University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

F ACTIN; NOTCH RECEPTOR; NOTCH1 RECEPTOR; UVOMORULIN; ACTIN; CADHERIN; HYBRID PROTEIN; METAL NANOPARTICLE; MICROSPHERE;

ARTICLE; CELLULAR DISTRIBUTION; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; CYTOGENETICS; DIFFUSION; FLUORESCENCE; HUMAN; HUMAN CELL; INTERCELLULAR SPACE; INTRACELLULAR SIGNALING; LIGAND BINDING; MECHANOGENETICS; MECHANOTRANSDUCTION; NANOPROBE; OLIGOMERIZATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN POLYMERIZATION; SINGLE CELL ANALYSIS; TIME; TRANSCRIPTION INITIATION; CELL CULTURE; CELL LINE; CHEMISTRY; GENETIC PROCEDURES; MECHANORECEPTOR; METABOLISM; PHYSIOLOGY; SPATIAL ANALYSIS;

ACTINS; CADHERINS; CELL LINE; CELLS, CULTURED; GENETIC TECHNIQUES; HUMANS; MECHANORECEPTORS; MECHANOTRANSDUCTION, CELLULAR; METAL NANOPARTICLES; MICROSPHERES; MOLECULAR PROBE TECHNIQUES; RECEPTORS, NOTCH; RECOMBINANT FUSION PROTEINS; SPATIAL ANALYSIS; TIME;

EID: 84966667300     PISSN: 00928674     EISSN: 10974172     Source Type: Journal    
DOI: 10.1016/j.cell.2017.06.005     Document Type: Erratum

References (44)

1. M. Banghart, K. Borges, E. Isacoff, D. Trauner, and R.H. Kramer Light-activated ion channels for remote control of neuronal firing Nat. Neurosci. 7 2004 1381 1386
2. A.A. Bharde, R. Palankar, C. Fritsch, A. Klaver, J.S. Kanger, T.M. Jovin, and D.J. Arndt-Jovin Magnetic nanoparticles as mediators of ligand-free activation of EGFR signaling PLoS ONE 8 2013 e68879
3. K.H. Biswas, K.L. Hartman, C.-H. Yu, O.J. Harrison, H. Song, A.W. Smith, W.Y.C. Huang, W.-C. Lin, Z. Guo, A. Padmanabhan, and et al. E-cadherin junction formation involves an active kinetic nucleation process Proc. Natl. Acad. Sci. USA 112 2015 10932 10937
4. C.D. Buckley, J. Tan, K.L. Anderson, D. Hanein, N. Volkmann, W.I. Weis, W.J. Nelson, and A.R. Dunn Cell adhesion. The minimal cadherin-catenin complex binds to actin filaments under force Science 346 2014 1254211
5. M.H. Cho, E.J. Lee, M. Son, J.-H. Lee, D. Yoo, J.-W. Kim, S.W. Park, J.-S. Shin, and J. Cheon A magnetic switch for the control of cell death signalling in in vitro and in vivo systems Nat. Mater. 11 2012 1038 1043
6. S. Cocco, R. Monasson, and J.F. Marko Force and kinetic barriers to unzipping of the DNA double helix Proc. Natl. Acad. Sci. USA 98 2001 8608 8613
7. K. Deisseroth Optogenetics Nat. Methods 8 2011 26 29
8. Y.F. Dufrêne, E. Evans, A. Engel, J. Helenius, H.E. Gaub, and D.J. Müller Five challenges to bringing single-molecule force spectroscopy into living cells Nat. Methods 8 2011 123 127
9. W. Engl, B. Arasi, L.L. Yap, J.P. Thiery, and V. Viasnoff Actin dynamics modulate mechanosensitive immobilization of E-cadherin at adherens junctions Nat. Cell Biol. 16 2014 587 594
10. F. Etoc, D. Lisse, Y. Bellaiche, J. Piehler, M. Coppey, and M. Dahan Subcellular control of Rac-GTPase signalling by magnetogenetic manipulation inside living cells Nat. Nanotechnol. 8 2013 193 198
11. J. Farlow, D. Seo, K.E. Broaders, M.J. Taylor, Z.J. Gartner, and Y.-W. Jun Formation of targeted monovalent quantum dots by steric exclusion Nat. Methods 10 2013 1203 1205
12. J. Gavard, M. Lambert, I. Grosheva, V. Marthiens, T. Irinopoulou, J.-F. Riou, A. Bershadsky, and R.-M. Mège Lamellipodium extension and cadherin adhesion: two cell responses to cadherin activation relying on distinct signalling pathways J. Cell Sci. 117 2004 257 270
13. Gay, G. (2014). Segmenting nuclei with skimage. http://damcb.com/segmenting-nuclei.html.
14. W.R. Gordon, D. Vardar-Ulu, G. Histen, C. Sanchez-Irizarry, J.C. Aster, and S.C. Blacklow Structural basis for autoinhibition of Notch Nat. Struct. Mol. Biol. 14 2007 295 300
15. W.R. Gordon, B. Zimmerman, L. He, L.J. Miles, J. Huang, K. Tiyanont, D.G. McArthur, J.C. Aster, N. Perrimon, J.J. Loparo, and S.C. Blacklow Mechanical allostery: evidence for a force requirement in the proteolytic activation of Notch Dev. Cell 33 2015 729 736
16. D. Ho, J.L. Zimmermann, F.A. Dehmelt, U. Steinbach, M. Erdmann, P. Severin, K. Falter, and H.E. Gaub Force-driven separation of short double-stranded DNA Biophys. J. 97 2009 3158 3167
17. C. Hoffmann, E. Mazari, S. Lallet, R. Le Borgne, V. Marchi, C. Gosse, and Z. Gueroui Spatiotemporal control of microtubule nucleation and assembly using magnetic nanoparticles Nat. Nanotechnol. 8 2013 199 205
18. T. Iskratsch, H. Wolfenson, and M.P. Sheetz Appreciating force and shape - the rise of mechanotransduction in cell biology Nat. Rev. Mol. Cell Biol. 15 2014 825 833
19. J.-T. Jang, H. Nah, J.-H. Lee, S.H. Moon, M.G. Kim, and J. Cheon Critical enhancements of MRI contrast and hyperthermic effects by dopant-controlled magnetic nanoparticles Angew. Chem. Int. Ed. Engl. 48 2009 1234 1238
20. I. Khait, Y. Orsher, O. Golan, U. Binshtok, N. Gordon-Bar, L. Amir-Zilberstein, and D. Sprinzak Quantitative analysis of Delta-like 1 membrane dynamics elucidates the role of contact geometry on Notch signaling Cell Rep. 14 2016 225 233
21. R. Kopan, and M.X.G. Ilagan The canonical Notch signaling pathway: unfolding the activation mechanism Cell 137 2009 216 233
22. B. Ladoux, E. Anon, M. Lambert, A. Rabodzey, P. Hersen, A. Buguin, P. Silberzan, and R.-M. Mège Strength dependence of cadherin-mediated adhesions Biophys. J. 98 2010 534 542
23. T. Lecuit, and A.S. Yap E-cadherin junctions as active mechanical integrators in tissue dynamics Nat. Cell Biol. 17 2015 533 539
24. A. Levskaya, O.D. Weiner, W.A. Lim, and C.A. Voigt Spatiotemporal control of cell signalling using a light-switchable protein interaction Nature 461 2009 997 1001
25. Z. Liu, Y. Liu, Y. Chang, H.R. Seyf, A. Henry, A.L. Mattheyses, K. Yehl, Y. Zhang, Z. Huang, and K. Salaita Nanoscale optomechanical actuators for controlling mechanotransduction in living cells Nat. Methods 13 2016 143 146
26. A. Louvi, and S. Artavanis-Tsakonas Notch signalling in vertebrate neural development Nat. Rev. Neurosci. 7 2006 93 102
27. R.J. Mannix, S. Kumar, F. Cassiola, M. Montoya-Zavala, E. Feinstein, M. Prentiss, and D.E. Ingber Nanomagnetic actuation of receptor-mediated signal transduction Nat. Nanotechnol. 3 2008 36 40
28. G. Miesenböck The optogenetic catechism Science 326 2009 395 399
29. M. Mosayebi, A.A. Louis, J.P.K. Doye, and T.E. Ouldridge Force-induced rupture of a DNA duplex: from fundamentals to force sensors ACS Nano 9 2015 11993 12003
30. K.C. Neuman, and A. Nagy Single-molecule force spectroscopy: optical tweezers, magnetic tweezers and atomic force microscopy Nat. Methods 5 2008 491 505
31. X. Peng, L.E. Cuff, C.D. Lawton, and K.A. DeMali Vinculin regulates cell-surface E-cadherin expression by binding to beta-catenin J. Cell Sci. 123 2010 567 577
32. S. Rakshit, and S. Sivasankar Biomechanics of cell adhesion: how force regulates the lifetime of adhesive bonds at the single molecule level Phys. Chem. Chem. Phys. 16 2014 2211 2223
33. N.J. Sniadecki, A. Anguelouch, M.T. Yang, C.M. Lamb, Z. Liu, S.B. Kirschner, Y. Liu, D.H. Reich, and C.S. Chen Magnetic microposts as an approach to apply forces to living cells Proc. Natl. Acad. Sci. USA 104 2007 14553 14558
34. D. Sprinzak, A. Lakhanpal, L. Lebon, L.A. Santat, M.E. Fontes, G.A. Anderson, J. Garcia-Ojalvo, and M.B. Elowitz Cis-interactions between Notch and Delta generate mutually exclusive signalling states Nature 465 2010 86 90
35. N.L. Stephenson, and J.M. Avis Direct observation of proteolytic cleavage at the S2 site upon forced unfolding of the Notch negative regulatory region Proc. Natl. Acad. Sci. USA 109 2012 E2757 E2765
36. J.E. Toettcher, C.A. Voigt, O.D. Weiner, and W.A. Lim The promise of optogenetics in cell biology: interrogating molecular circuits in space and time Nat. Methods 8 2011 35 38
37. P. Tseng, J.W. Judy, and D. Di Carlo Magnetic nanoparticle-mediated massively parallel mechanical modulation of single-cell behavior Nat. Methods 9 2012 1113 1119
38. F. van Roy Beyond E-cadherin: roles of other cadherin superfamily members in cancer Nat. Rev. Cancer 14 2014 121 134
39. V. Vogel, and M. Sheetz Local force and geometry sensing regulate cell functions Nat. Rev. Mol. Cell Biol. 7 2006 265 275
40. X. Wang, and T. Ha Defining single molecular forces required to activate integrin and notch signaling Science 340 2013 991 994
41. H. Wang, D.W. Brandl, P. Nordlander, and N.J. Halas Plasmonic nanostructures: artificial molecules Acc. Chem. Res. 40 2007 53 62
42. R.J. Weber, S.I. Liang, N.S. Selden, T.A. Desai, and Z.G. Gartner Efficient targeting of fatty-acid modified oligonucleotides to live cell membranes through stepwise assembly Biomacromolecules 15 2014 4621 4626
43. S.K. Wu, G.A. Gomez, M. Michael, S. Verma, H.L. Cox, J.G. Lefevre, R.G. Parton, N.A. Hamilton, Z. Neufeld, and A.S. Yap Cortical F-actin stabilization generates apical-lateral patterns of junctional contractility that integrate cells into epithelia Nat. Cell Biol. 16 2014 167 178
44. M. Yao, W. Qiu, R. Liu, A.K. Efremov, P. Cong, R. Seddiki, M. Payre, C.T. Lim, B. Ladoux, R.-M. Mège, and J. Yan Force-dependent conformational switch of α-catenin controls vinculin binding Nat. Commun. 5 2014 4525