16 results match your criteria: "Buchmann Institute for Molecular Life Sciences and Institute for Biophysics[Affiliation]"

Pyridylpiperazine efflux pump inhibitor boosts in vivo antibiotic efficacy against K. pneumoniae.

EMBO Mol Med

January 2024

Univ. Lille, Inserm, Institut Pasteur de Lille, U1177 - Drugs and Molecules for Living Systems, F-59000, Lille, France.

Antimicrobial resistance is a global problem, rendering conventional treatments less effective and requiring innovative strategies to combat this growing threat. The tripartite AcrAB-TolC efflux pump is the dominant constitutive system by which Enterobacterales like Escherichia coli and Klebsiella pneumoniae extrude antibiotics. Here, we describe the medicinal chemistry development and drug-like properties of BDM91288, a pyridylpiperazine-based AcrB efflux pump inhibitor.

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ArtiaX: An electron tomography toolbox for the interactive handling of sub-tomograms in UCSF ChimeraX.

Protein Sci

December 2022

Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Goethe University Frankfurt, Frankfurt, Germany.

Article Synopsis
  • Cryo-electron tomography analysis focuses on selecting macromolecular complexes for averaging and structure determination.
  • A new UCSF ChimeraX plugin enables users to display, select, and edit particles in tomograms, with real-time modifications and exports to various file formats.
  • The plugin enhances user experience with customizable particle visualization and is designed for intuitive use, making it accessible even for those without specialized knowledge.
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Cell-free expression enables direct cotranslational insertion of G protein coupled receptors (GPCRs) and other membrane proteins into the defined membrane environments of nanodiscs. This technique avoids GPCR contacts with detergents and allows rapid identification of lipid effects on GPCR function as well as fast screening of receptor derivatives. Critical steps of conventional GPCR preparation from cellular membranes followed by detergent-based reconstitution into nanodisc membranes are thus eliminated.

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Mean curvature motion facilitates the segmentation and surface visualization of electron tomograms.

J Struct Biol

March 2022

Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Goethe University Frankfurt, Max-von-Laue-Str. 15, D-60438 Frankfurt am Main, Germany. Electronic address:

Three-dimensional visualization of biological samples is essential for understanding their architecture and function. However, it is often challenging due to the macromolecular crowdedness of the samples and low signal-to-noise ratio of the cryo-electron tomograms. Denoising and segmentation techniques address this challenge by increasing the signal-to-noise ratio and by simplifying the data in images.

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It's noisy out there! A review of denoising techniques in cryo-electron tomography.

J Struct Biol

December 2021

Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Goethe University Frankfurt Max-von-Laue-Str. 15, Frankfurt am Main, D-60438, Germany. Electronic address:

Cryo-electron tomography is the only technique that can provide sub-nanometer resolved images of cell regions or even whole cells, without the need of labeling or staining methods. Technological advances over the past decade in electron microscope stability, cameras, stage precision and software have resulted in faster acquisition speeds and considerably improved resolution. In pursuit of even better image resolution, researchers seek to reduce noise - a crucial factor affecting the reliability of the tomogram interpretation and ultimately limiting the achieved resolution.

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Ex vivo visualization of RNA polymerase III-specific gene activity with electron microscopy.

Commun Biol

February 2021

Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Goethe University Frankfurt, 60438, Frankfurt am Main, Germany.

The direct study of transcription or DNA-protein-binding events, requires imaging of individual genes at molecular resolution. Electron microscopy (EM) can show local detail of the genome. However, direct visualization and analysis of specific individual genes is currently not feasible as they cannot be unambiguously localized in the crowded, landmark-free environment of the nucleus.

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FIB-SEM imaging properties of Drosophila melanogaster tissues embedded in Lowicryl HM20.

J Microsc

February 2019

Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Goethe-University, Frankfurt am Main, Germany.

Lowicryl resins enable processing of biological material for electron microscopy at the lowest temperatures compatible with resin embedding. When combined with high-pressure freezing and freeze-substitution, Lowicryl embedding supports preservation of fine structural details and fluorescent markers. Here, we analysed the applicability of Lowicryl HM20 embedding for focused ion beam (FIB) scanning electron microscopy (SEM) tomography of Drosophila melanogaster embryonic and larval model systems.

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Parkinson's disease (PD) is a frequent neurodegenerative process in old age. Accumulation and aggregation of the lipid-binding SNARE complex component α-synuclein (SNCA) underlies this vulnerability and defines stages of disease progression. Determinants of SNCA levels and mechanisms of SNCA neurotoxicity have been intensely investigated.

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Structure of RNA polymerase I transcribing ribosomal DNA genes.

Nature

December 2016

Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Goethe University Frankfurt, Max-von-Laue Str. 15, Frankfurt 60438, Germany.

RNA polymerase I (Pol I) is a highly processive enzyme that transcribes ribosomal DNA (rDNA) and regulates growth of eukaryotic cells. Crystal structures of free Pol I from the yeast Saccharomyces cerevisiae have revealed dimers of the enzyme stabilized by a 'connector' element and an expanded cleft containing the active centre in an inactive conformation. The central bridge helix was unfolded and a Pol-I-specific 'expander' element occupied the DNA-template-binding site.

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A flexible, multilayered protein scaffold maintains the slit in between glomerular podocytes.

JCI Insight

June 2016

Department of Medicine, Division of Nephrology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Vertebrate life critically depends on renal filtration and excretion of low molecular weight waste products. This process is controlled by a specialized cell-cell contact between podocyte foot processes: the slit diaphragm (SD). Using a comprehensive set of targeted KO mice of key SD molecules, we provided genetic, functional, and high-resolution ultrastructural data highlighting a concept of a flexible, dynamic, and multilayered architecture of the SD.

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Three-dimensional CTF correction improves the resolution of electron tomograms.

J Struct Biol

February 2017

Goethe University Frankfurt, Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Max-von-Laue Str. 15, 60438 Frankfurt am Main, Germany. Electronic address:

Correction of the contrast transfer function (CTF) of the microscope is a necessary step, in order to achieve high resolution from averaged electron microscopic images. Thereby, the CTF is first estimated and subsequently the electron micrograph is corrected, so that the negative oscillations of the CTF are equalized. Typically, the CTF correction is performed in 2D and the tilt-induced focus gradient is taken into account.

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M-free: Mask-independent scoring of the reference bias.

J Struct Biol

November 2015

Goethe University Frankfurt, Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Max-von-Laue Str.15, 60438 Frankfurt am Main, Germany. Electronic address:

The M-free score is a heuristic to measure the reference bias in applications such as template matching and sub-tomogram averaging. In the original formulation the mask typically used in these applications had to be separated into a working and a testing area. Here we present a variant of the calculation of the M-free score, which under certain conditions does not require adapting the mask used during the processing.

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The closure of epidermal openings is an essential biological process that causes major developmental problems such as spina bifida in humans if it goes awry. At present, the mechanism of closure remains elusive. Therefore, we reconstructed a model closure event, dorsal closure in fly embryos, by large-volume correlative electron tomography.

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Super-sampling SART with ordered subsets.

J Struct Biol

November 2014

Goethe University Frankfurt, Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Max-von-Laue Str. 15, 60438 Frankfurt am Main, Germany. Electronic address:

In tomography, the quality of the reconstruction is essential because the complete cascade of the subsequent analysis is based on it. To date, weighted back-projection (WBP) has been the most commonly used technique due to its versatility and performance in sub-tomogram averaging. Here we present super-sampling SART that is based on the simultaneous algebraic reconstruction technique.

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M-free: scoring the reference bias in sub-tomogram averaging and template matching.

J Struct Biol

July 2014

Goethe University Frankfurt, Buchmann Institute for Molecular Life Sciences and Institute for Biophysics, Max-von-Laue Str.15, 60438 Frankfurt am Main, Germany. Electronic address:

Cryo-electron tomography provides a snapshot of the cellular proteome. With template matching, the spatial positions of various macromolecular complexes within their native cellular context can be detected. However, the growing awareness of the reference bias introduced by the cross-correlation based approaches, and more importantly the lack of a reliable confidence measurement in the selection of these macromolecular complexes, has restricted the use of these applications.

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Correlative microscopy incorporates the specificity of fluorescent protein labeling into high-resolution electron micrographs. Several approaches exist for correlative microscopy, most of which have used the green fluorescent protein (GFP) as the label for light microscopy. Here we use chemical tagging and synthetic fluorophores instead, in order to achieve protein-specific labeling, and to perform multicolor imaging.

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