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Bacterial Pathogenesis

Overview of attention for book
Cover of 'Bacterial Pathogenesis'

Table of Contents

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    Book Overview
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    Chapter 1 Protein-Based Strategies to Identify and Isolate Bacterial Virulence Factors.
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    Chapter 2 Analysis of Bacterial Surface Interactions with Mass Spectrometry-Based Proteomics.
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    Chapter 3 Differential Radial Capillary Action of Ligand Assay (DRaCALA) for High-Throughput Detection of Protein-Metabolite Interactions in Bacteria.
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    Chapter 4 Identifying Bacterial Immune Evasion Proteins Using Phage Display.
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    Chapter 5 Competition for Iron Between Host and Pathogen: A Structural Case Study on Helicobacter pylori.
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    Chapter 6 Common Challenges in Studying the Structure and Function of Bacterial Proteins: Case Studies from Helicobacter pylori.
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    Chapter 7 Development of a Single Locus Sequence Typing (SLST) Scheme for Typing Bacterial Species Directly from Complex Communities.
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    Chapter 8 Reconstructing the Ancestral Relationships Between Bacterial Pathogen Genomes.
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    Chapter 9 Making Fluorescent Streptococci and Enterococci for Live Imaging.
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    Chapter 10 Computer Vision-Based Image Analysis of Bacteria.
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    Chapter 11 Assessing Vacuolar Escape of Listeria Monocytogenes.
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    Chapter 12 Immobilization Techniques of Bacteria for Live Super-resolution Imaging Using Structured Illumination Microscopy.
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    Chapter 13 Negative Staining and Transmission Electron Microscopy of Bacterial Surface Structures.
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    Chapter 14 Detection of Intracellular Proteins by High-Resolution Immunofluorescence Microscopy in Streptococcus pyogenes.
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    Chapter 15 Antibody Guided Molecular Imaging of Infective Endocarditis.
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    Chapter 16 The Zebrafish as a Model for Human Bacterial Infections.
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    Chapter 17 Determining Platelet Activation and Aggregation in Response to Bacteria.
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    Chapter 18 Killing Bacteria with Cytotoxic Effector Proteins of Human Killer Immune Cells: Granzymes, Granulysin, and Perforin.
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    Chapter 19 In Vitro and In Vivo Biofilm Formation by Pathogenic Streptococci.
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    Chapter 20 Murine Mycobacterium marinum Infection as a Model for Tuberculosis.
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    Chapter 21 Generating and Purifying Fab Fragments from Human and Mouse IgG Using the Bacterial Enzymes IdeS, SpeB and Kgp.
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    Chapter 22 Measuring Antibody Orientation at the Bacterial Surface.
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    Chapter 23 Toward Clinical use of the IgG Specific Enzymes IdeS and EndoS against Antibody-Mediated Diseases.
Attention for Chapter 21: Generating and Purifying Fab Fragments from Human and Mouse IgG Using the Bacterial Enzymes IdeS, SpeB and Kgp.
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Chapter title
Generating and Purifying Fab Fragments from Human and Mouse IgG Using the Bacterial Enzymes IdeS, SpeB and Kgp.
Chapter number 21
Book title
Bacterial Pathogenesis
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6673-8_21
Pubmed ID
Book ISBNs
978-1-4939-6671-4, 978-1-4939-6673-8
Authors

Jonathan Sjögren Ph.D., Linda Andersson M.Sc., Malin Mejàre Ph.D., Fredrik Olsson M.Sc., Jonathan Sjögren, Linda Andersson, Malin Mejàre, Fredrik Olsson

Editors

Pontus Nordenfelt, Mattias Collin

Abstract

Fab fragments are valuable research tools in various areas of science including applications in imaging, binding studies, removal of Fc-mediated effector functions, mass spectrometry, infection biology, and many others. The enzymatic tools for the generation of Fab fragments have been discovered through basic research within the field of molecular bacterial pathogenesis. Today, these enzymes are widely applied as research tools and in this chapter, we describe methodologies based on bacterial enzymes to generate Fab fragments from both human and mouse IgG. For all human IgG subclasses, the IdeS enzyme from Streptococcus pyogenes has been applied to generate F(ab')2 fragments that subsequently can be reduced under mild conditions to generate a homogenous pool of Fab' fragments. The enzyme Kgp from Porphyromonas gingivalis has been applied to generate intact Fab fragments from human IgG1 and the Fab fragments can be purified using a CH1-specific affinity resin. The SpeB protease, also from S. pyogenes, is able to digest mouse IgGs and has been applied to digest antibodies and Fab fragments can be purified on light chain affinity resins. In this chapter, we describe methodologies that can be used to obtain Fab fragments from human and mouse IgG using bacterial proteases.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 16 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 16 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 25%
Researcher 3 19%
Student > Bachelor 2 13%
Student > Ph. D. Student 1 6%
Lecturer 1 6%
Other 2 13%
Unknown 3 19%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 31%
Medicine and Dentistry 3 19%
Pharmacology, Toxicology and Pharmaceutical Science 1 6%
Immunology and Microbiology 1 6%
Agricultural and Biological Sciences 1 6%
Other 0 0%
Unknown 5 31%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 04 January 2017.
All research outputs
#15,398,970
of 22,908,162 outputs
Outputs from Methods in molecular biology
#5,357
of 13,132 outputs
Outputs of similar age
#256,356
of 420,477 outputs
Outputs of similar age from Methods in molecular biology
#465
of 1,074 outputs
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So far Altmetric has tracked 13,132 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 44th percentile – i.e., 44% of its peers scored the same or lower than it.
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