Search Results - "Mcnally, James G."
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Single-molecule analysis of transcription factor binding at transcription sites in live cells
Published in Nature communications (18-07-2014)“…Although numerous live-cell measurements have shown that transcription factors (TFs) bind chromatin transiently, no measurements of transient binding have been…”
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Regulation of RNA polymerase II activation by histone acetylation in single living cells
Published in Nature (London) (11-12-2014)“…The interplay of histone acetylation and RNA polymerase II activity is investigated using fluorescence microscopy; acetylation of H3 at Lys 27 enhances the…”
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Minimizing the Impact of Photoswitching of Fluorescent Proteins on FRAP Analysis
Published in Biophysical journal (04-04-2012)“…Fluorescence recovery after photobleaching (FRAP) is a widely used imaging technique for measuring the mobility of fluorescently tagged proteins in living…”
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4
FRAP and kinetic modeling in the analysis of nuclear protein dynamics: what do we really know?
Published in Current opinion in cell biology (01-06-2010)“…The binding of nuclear proteins to chromatin in live cells has been analyzed by kinetic modeling procedures applied to experimental data from fluorescence…”
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Unraveling heme detoxification in the malaria parasite by in situ correlative X-ray fluorescence microscopy and soft X-ray tomography
Published in Scientific reports (08-08-2017)“…A key drug target for malaria has been the detoxification pathway of the iron-containing molecule heme, which is the toxic byproduct of hemoglobin digestion…”
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Photoswitching-free FRAP analysis with a genetically encoded fluorescent tag
Published in PloS one (18-09-2014)“…Fluorescence recovery after photobleaching (FRAP) is a widely used imaging technique for measuring protein dynamics in live cells that has provided many…”
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Measuring Chromatin Interaction Dynamics on the Second Time Scale at Single-Copy Genes
Published in Science (American Association for the Advancement of Science) (18-10-2013)“…The chromatin immunoprecipitation (ChIP) assay is widely used to capture interactions between chromatin and regulatory proteins, but it is unknown how stable…”
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Analysis of Binding Reactions by Fluorescence Recovery after Photobleaching
Published in Biophysical journal (01-06-2004)“…Fluorescence recovery after photobleaching (FRAP) is now widely used to investigate binding interactions in live cells. Although various idealized solutions…”
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Changes in Chromatin Structure and Mobility in Living Cells at Sites of DNA Double-Strand Breaks
Published in The Journal of cell biology (13-03-2006)“…The repair of DNA double-strand breaks (DSBs) is facilitated by the phosphorylation of H2AX, which organizes DNA damage signaling and chromatin remodeling…”
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Cross-Validating FRAP and FCS to Quantify the Impact of Photobleaching on In Vivo Binding Estimates
Published in Biophysical journal (03-11-2010)“…Binding can now be quantified in live cells, but the accuracy of such measurements remains uncertain. To address this uncertainty, we compare fluorescence…”
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Prion Induction by the Short-Lived, Stress-Induced Protein Lsb2 Is Regulated by Ubiquitination and Association with the Actin Cytoskeleton
Published in Molecular cell (22-07-2011)“…Yeast prions are self-perpetuating, QN-rich amyloids that control heritable traits and serve as a model for mammalian amyloidoses. De novo prion formation by…”
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Dissecting the binding mechanism of the linker histone in live cells: an integrated FRAP analysis
Published in The EMBO journal (07-04-2010)“…The linker histone H1 has a fundamental role in DNA compaction. Although models for H1 binding generally involve the H1 C‐terminal tail and sites S1 and S2…”
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Direct Measurement of Association and Dissociation Rates of DNA Binding in Live Cells by Fluorescence Correlation Spectroscopy
Published in Biophysical journal (08-07-2009)“…Measurement of live-cell binding interactions is vital for understanding the biochemical reactions that drive cellular processes. Here, we develop,…”
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Concurrent Fast and Slow Cycling of a Transcriptional Activator at an Endogenous Promoter
Published in Science (American Association for the Advancement of Science) (25-01-2008)“…For gene regulation, some transcriptional activators bind periodically to promoters with either a fast (~1 minute) or a slow (~15 to 90 minutes) cycle. It is…”
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Highly stable loading of Mcm proteins onto chromatin in living cells requires replication to unload
Published in The Journal of cell biology (10-01-2011)“…The heterohexameric minichromosome maintenance protein complex (Mcm2-7) functions as the eukaryotic helicase during DNA replication. Mcm2-7 loads onto…”
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Hsp90 Inhibition Transiently Activates Src Kinase and Promotes Src-Dependent Akt and Erk Activation
Published in Proceedings of the National Academy of Sciences - PNAS (25-07-2006)“…Hsp90 plays an essential role in maintaining stability and activity of its clients, including oncogenic signaling proteins that regulate key signal…”
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Towards an atlas of mammalian cell ultrastructure by cryo soft X-ray tomography
Published in Journal of structural biology (01-02-2012)“…We provide a catalog of 3D cryo soft X-ray tomography (cryo-SXT) images obtained from ∼6 to 12μm thick mouse adenocarcinoma cells. Included are multiple…”
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Assembly of the transcription machinery: ordered and stable, random and dynamic, or both?
Published in Chromosoma (01-12-2011)“…The assembly of the transcription machinery is a key step in gene activation, but even basic details of this process remain unclear. Here we discuss the…”
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Rapid Glucocorticoid Receptor Exchange at a Promoter Is Coupled to Transcription and Regulated by Chaperones and Proteasomes
Published in Molecular and Cellular Biology (01-04-2004)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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A Reaction-Diffusion Model to Study RNA Motion by Quantitative Fluorescence Recovery after Photobleaching
Published in Biophysical journal (15-04-2007)“…Fluorescence recovery after photobleaching (FRAP) is a powerful technique to study molecular dynamics inside living cells. During the past years, several…”
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