0000000000012758

AUTHOR

Udo Birk

0000-0001-6313-7475

showing 8 related works from this author

Nanoscale distribution of TLR4 on primary human macrophages stimulated with LPS and ATI

2019

Toll-like receptor 4 (TLR4) plays a crucial role in the recognition of invading pathogens. Upon activation by lipopolysaccharides (LPS), TLR4 is recruited into specific membrane domains and dimerizes. In addition to LPS, TLR4 can be stimulated by wheat amylase-trypsin inhibitors (ATI). ATI are proteins associated with gluten containing grains, whose ingestion promotes intestinal and extraintestinal inflammation. However, the effect of ATI vs. LPS on the membrane distribution of TLR4 at the nanoscale has not been analyzed. In this study, we investigated the effect of LPS and ATI stimulation on the membrane distribution of TLR4 in primary human macrophages using single molecule localization m…

LipopolysaccharidesSingle molecule localizationStimulationInflammation02 engineering and technology010402 general chemistry01 natural sciencesmedicineHumansDistribution (pharmacology)General Materials ScienceReceptorCells CulturedChemistryMacrophagesCell Membrane021001 nanoscience & nanotechnology0104 chemical sciencesCell biologyToll-Like Receptor 4MembraneMicroscopy FluorescenceTLR4lipids (amino acids peptides and proteins)Receptor clusteringmedicine.symptomTrypsin Inhibitors0210 nano-technologyNanoscale
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Super-resolved linear fluorescence localization microscopy using photostable fluorophores: A virtual microscopy study

2017

Abstract Current approaches to overcome the conventional limit of the resolution potential of light microscopy (of about 200 nm for visible light), often suffer from non-linear effects, which render the quantification of the image intensities in the reconstructions difficult, and also affect the quantification of the biological structure under investigation. As an attempt to face these difficulties, we discuss a particular method of localization microscopy which is based on photostable fluorescent dyes. The proposed method can potentially be implemented as a fast alternative for quantitative localization microscopy, circumventing the need for the acquisition of thousands of image frames and…

0301 basic medicineMaterials sciencebusiness.industryMultispectral imageResolution (electron density)02 engineering and technology021001 nanoscience & nanotechnologyFluorescenceAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materials03 medical and health sciences030104 developmental biologyOpticsMicroscopyCalibrationPhotoactivated localization microscopyElectrical and Electronic EngineeringPhysical and Theoretical Chemistry0210 nano-technologybusinessVirtual microscopyVisible spectrumOptics Communications
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Super-resolution binding activated localization microscopy through reversible change of DNA conformation

2018

ABSTRACT Methods of super-resolving light microscopy (SRM) have found an exponentially growing range of applications in cell biology, including nuclear structure analyses. Recent developments have proven that Single Molecule Localization Microscopy (SMLM), a type of SRM, is particularly useful for enhanced spatial analysis of the cell nucleus due to its highest resolving capability combined with very specific fluorescent labeling. In this commentary we offer a brief review of the latest methodological development in the field of SMLM of chromatin designated DNA Structure Fluctuation Assisted Binding Activated Localization Microscopy (abbreviated as fBALM) as well as its potential future app…

0301 basic medicineSingle molecule localization03 medical and health scienceschemistry.chemical_compound0302 clinical medicinesuper-resolution microscopyMicroscopyfBALMmedicineSMLMsingle molecule localizationCell NucleusBinding SitesSuper-resolution microscopyExtra ViewnucleusDNACell BiologySuperresolutionSingle Molecule ImagingChromatinfBALM SMLMCell nucleus030104 developmental biologymedicine.anatomical_structurechemistry030220 oncology & carcinogenesisBiophysicschromatinNucleic Acid ConformationNucleusDNANucleus
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High-resolution deep view microscopy of cells and tissues

2020

Abstract Methods, experimental setups and perspectives of three-dimensional deep view imaging microscopy of cell or tissue samples are reported. Preliminary biophysical and clinically relevant examples are presented.

Materials scienceNuclear magnetic resonanceAxial tomographyMicroscopyHigh resolutionStatistical and Nonlinear PhysicsElectrical and Electronic Engineering3d microscopySuperresolutionFluorescenceAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsQuantum Electronics
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Localization microscopy of DNA in situ using Vybrant(®) DyeCycle™ Violet fluorescent probe: A new approach to study nuclear nanostructure at single m…

2016

Higher order chromatin structure is not only required to compact and spatially arrange long chromatids within a nucleus, but have also important functional roles, including control of gene expression and DNA processing. However, studies of chromatin nanostructures cannot be performed using conventional widefield and confocal microscopy because of the limited optical resolution. Various methods of superresolution microscopy have been described to overcome this difficulty, like structured illumination and single molecule localization microscopy. We report here that the standard DNA dye Vybrant(®) DyeCycle™ Violet can be used to provide single molecule localization microscopy (SMLM) images of …

0301 basic medicine02 engineering and technologyBiologyChromosomeslaw.inventionVybrant DyeCycle Violet03 medical and health sciencesDNA dyesHigher Order Chromatin StructureConfocal microscopylawphotoconversionMicroscopyChlorocebus aethiopsAnimalsdSTORMSMLMVero CellsFluorescent Dyeschromatin structureCell NucleusResolution (electron density)DNA replicationCell BiologyDNA021001 nanoscience & nanotechnologySingle Molecule ImagingFluorescenceSingle Molecule ImagingChromatinCell biologyNanostructures030104 developmental biologyDrosophila melanogasterMicroscopy FluorescenceBiophysics0210 nano-technologyExperimental cell research
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Single molecule localization microscopy of the distribution of chromatin using Hoechst and DAPI fluorescent probes.

2014

Several approaches have been described to fluorescently label and image DNA and chromatin in situ on the single-molecule level. These superresolution microscopy techniques are based on detecting optically isolated, fluorescently tagged anti-histone antibodies, fluorescently labeled DNA precursor analogs, or fluorescent dyes bound to DNA. Presently they suffer from various drawbacks such as low labeling efficiency or interference with DNA structure. In this report, we demonstrate that DNA minor groove binding dyes, such as Hoechst 33258, Hoechst 33342, and DAPI, can be effectively employed in single molecule localization microscopy (SMLM) with high optical and structural resolution. Upon ill…

DNA ReplicationHoechstDNA RepairDNA repairBiologyfluorescence microscopyDAPIchemistry.chemical_compoundphotoconversionsuper-resolution microscopylocalization microscopyFluorescence microscopeSPDMAnimalsHumansDAPIdSTORMSMLMFluorescent DyesMicroscopySuper-resolution microscopynucleusDNA replicationdSTORCell BiologyDNADNA Minor Groove BindingChromatinChromatinCell biologychemistryMicroscopy FluorescencechromatinblinkingDNAResearch PaperNucleus (Austin, Tex.)
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Quantitative super-resolution localization microscopy of DNA in situ using Vybrant® DyeCycle™ Violet fluorescent probe.

2016

Single Molecule Localization Microscopy (SMLM) is a recently emerged optical imaging method that was shown to achieve a resolution in the order of tens of nanometers in intact cells. Novel high resolution imaging methods might be crucial for understanding of how the chromatin, a complex of DNA and proteins, is arranged in the eukaryotic cell nucleus. Such an approach utilizing switching of a fluorescent, DNA-binding dye Vybrant® DyeCycle™ Violet has been previously demonstrated by us (Żurek-Biesiada et al., 2015) [1]. Here we provide quantitative information on the influence of the chemical environment on the behavior of the dye, discuss the variability in the DNA-associated signal density,…

0301 basic medicineIn situMaterials sciencevybrant violetLocalization microscopyNanotechnologysuper-resolutionlcsh:Computer applications to medicine. Medical informaticsFluorescenceNucleus03 medical and health scienceschemistry.chemical_compound0302 clinical medicineMicroscopylocalization microscopySingle moleculesmedicinedSTORMlcsh:Science (General)Data ArticleMultidisciplinarySuper-ResolutionResolution (electron density)nucleusVybrant violetDNA dyeDNAFluorescenceSuperresolutionChromatinChromatin030104 developmental biologymedicine.anatomical_structurechemistry030220 oncology & carcinogenesischromatinlcsh:R858-859.7fluorescencesingle moleculesNucleusDNAlcsh:Q1-390Data in brief
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Chess recognition using 3D patterned illumination camera

2021

Computer Vision has been applied to augment traditional board games such as Chess for a number of reasons. While augmented reality enhances the gaming experience, the required additional hardware (e.g. head gear) is still not widely accepted in everyday leisure activities, and therefore, camera based methods have been developed to interface the computer with the real-life chess board. However, traditional 2D camera approaches suffer from ill-defined environmental conditions (lighting, viewing angle) and are therefore severely limited in their application. To answer this issue, we have incorporated a consumer-grade depth camera based on patterned illumination. We could show that in combinati…

Computer programComputer sciencebusiness.industryHead (linguistics)Interface (computing)ComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONComputingMilieux_PERSONALCOMPUTINGRGB color modelAugmented realityComputer visionArtificial intelligenceViewing anglebusinessThirteenth International Conference on Machine Vision
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