Literature DB >> 19475385

Automated live microscopy to study mitotic gene function in fluorescent reporter cell lines.

Michael H A Schmitz1, Daniel W Gerlich.   

Abstract

Fluorescence live microscopy is a powerful technique to study complex cellular dynamics such as cell division. The availability of fluorescent markers based on GFP fusion proteins for virtually any cellular structure allows efficient visualization of specific processes, and the combination of different fluorophores can be used to study their coordination. In this chapter, we present methods for automated live cell microscopy to study mitotic gene function systematically and in high throughput. In particular, we provide protocols for efficient generation of fluorescent reporter cell lines stably expressing combinations of cellular markers, and provide detailed guidelines for optimizing imaging protocols for automated long-term live microscopy.

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Year:  2009        PMID: 19475385     DOI: 10.1007/978-1-60327-993-2_7

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  13 in total

1.  Unsupervised modeling of cell morphology dynamics for time-lapse microscopy.

Authors:  Qing Zhong; Alberto Giovanni Busetto; Juan P Fededa; Joachim M Buhmann; Daniel W Gerlich
Journal:  Nat Methods       Date:  2012-05-27       Impact factor: 28.547

2.  CellCognition: time-resolved phenotype annotation in high-throughput live cell imaging.

Authors:  Michael Held; Michael H A Schmitz; Bernd Fischer; Thomas Walter; Beate Neumann; Michael H Olma; Matthias Peter; Jan Ellenberg; Daniel W Gerlich
Journal:  Nat Methods       Date:  2010-08-08       Impact factor: 28.547

3.  Augmin accumulation on long-lived microtubules drives amplification and kinetochore-directed growth.

Authors:  Ana F David; Philippe Roudot; Wesley R Legant; Eric Betzig; Gaudenz Danuser; Daniel W Gerlich
Journal:  J Cell Biol       Date:  2019-05-21       Impact factor: 10.539

4.  LOVTRAP: A Versatile Method to Control Protein Function with Light.

Authors:  Hui Wang; Klaus M Hahn
Journal:  Curr Protoc Cell Biol       Date:  2016-12-01

Review 5.  Automated microscopy for high-content RNAi screening.

Authors:  Christian Conrad; Daniel W Gerlich
Journal:  J Cell Biol       Date:  2010-02-22       Impact factor: 10.539

6.  Sds22 and Repo-Man stabilize chromosome segregation by counteracting Aurora B on anaphase kinetochores.

Authors:  Claudia Wurzenberger; Michael Held; Michael A Lampson; Ina Poser; Anthony A Hyman; Daniel W Gerlich
Journal:  J Cell Biol       Date:  2012-07-16       Impact factor: 10.539

7.  TRACMIT: An effective pipeline for tracking and analyzing cells on micropatterns through mitosis.

Authors:  Olivier Burri; Benita Wolf; Arne Seitz; Pierre Gönczy
Journal:  PLoS One       Date:  2017-07-26       Impact factor: 3.240

8.  Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.

Authors:  Beata E Mierzwa; Nicolas Chiaruttini; Lorena Redondo-Morata; Joachim Moser von Filseck; Julia König; Jorge Larios; Ina Poser; Thomas Müller-Reichert; Simon Scheuring; Aurélien Roux; Daniel W Gerlich
Journal:  Nat Cell Biol       Date:  2017-06-12       Impact factor: 28.824

9.  Live-cell imaging RNAi screen identifies PP2A-B55alpha and importin-beta1 as key mitotic exit regulators in human cells.

Authors:  Michael H A Schmitz; Michael Held; Veerle Janssens; James R A Hutchins; Otto Hudecz; Elitsa Ivanova; Jozef Goris; Laura Trinkle-Mulcahy; Angus I Lamond; Ina Poser; Anthony A Hyman; Karl Mechtler; Jan-Michael Peters; Daniel W Gerlich
Journal:  Nat Cell Biol       Date:  2010-08-15       Impact factor: 28.824

10.  Ki-67 acts as a biological surfactant to disperse mitotic chromosomes.

Authors:  Sara Cuylen; Claudia Blaukopf; Antonio Z Politi; Thomas Müller-Reichert; Beate Neumann; Ina Poser; Jan Ellenberg; Anthony A Hyman; Daniel W Gerlich
Journal:  Nature       Date:  2016-06-29       Impact factor: 49.962

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