Titlebook: Bacterial Pathogenesis; Methods and Protocol Pontus Nordenfelt,Mattias Collin Book 2023Latest edition The Editor(s) (if applicable) and The

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Affinity-Purification Combined with Crosslinking Mass Spectrometry for Identification and Structuralization as well as immune evasion. In bacteria, these interactions most often involve specialized virulence factors or effector proteins that specifically target central host proteins. Here, I present a mass spectrometry-based proteomics approach starting with the identification of host–pathogen int

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Elucidating the Stoichiometries of Host–Pathogen Protein Interactions with Mass Photometryhe Refeyn One. to investigate molecular complexes, using the M53 protein, a plasminogen-binding group A . M-like protein (PAM), and human plasminogen as exemplar proteins. The methodology described herein confirmed a 1:1 binding stoichiometry for the M53–plasminogen complex. Additionally, MP was use

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Identification of Substrates of Secreted Bacterial Protease by APEX2-Based Proximity Labelingion with high-resolution quantitative mass spectrometry to profile the substrates of . HtrA protease on the membrane of human stomach epithelial cells. This strategy can be further applied to identify other interactions between secreted bacterial virulence factors and host receptors on live cells.

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https://doi.org/10.1007/978-3-322-91012-7ures such as RNA quantification and DNase treatment are also included to ensure amount and quality of the RNA samples. The second part of the chapter includes a method used to analyze bacterial gene expression (Northern blotting), two methods to generate radioactive probes, as well as target detection using a phosphorimager.

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Controllingorganisation in Bankennalyses that accounts for the disruptive effect of recombination. This allows users to investigate the recombination events that have occurred, as well as to produce more meaningful phylogenetic analyses which recover the clonal genealogy representing the clonal relationships between genomes.

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Alfred Marusev,Andreas Pfingsten-efficient method. It enables precise quantification even from very small amounts of target DNA. This method also enables analysis of complex samples with large amounts of interfering DNA, such as infected tissues or microbiome studies.

只看該作者 · 發(fā)表于 2025-3-25 00:39:06

Total Bacterial RNA Isolation and Northern Blotting Analysisures such as RNA quantification and DNase treatment are also included to ensure amount and quality of the RNA samples. The second part of the chapter includes a method used to analyze bacterial gene expression (Northern blotting), two methods to generate radioactive probes, as well as target detection using a phosphorimager.

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