↓ Skip to main content

The BAM Complex

Overview of attention for book
Cover of 'The BAM Complex'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 The β-Barrel Assembly Machinery Complex
  3. Altmetric Badge
    Chapter 2 Yeast Mitochondria as a Model System to Study the Biogenesis of Bacterial β-Barrel Proteins.
  4. Altmetric Badge
    Chapter 3 Experimental Methods for Studying the BAM Complex in Neisseria meningitidis
  5. Altmetric Badge
    Chapter 4 Heat Modifiability of Outer Membrane Proteins from Gram-Negative Bacteria
  6. Altmetric Badge
    Chapter 5 The Role of a Destabilized Membrane for OMP Insertion
  7. Altmetric Badge
    Chapter 6 Treponema pallidum in Gel Microdroplets: A Method for Topological Analysis of BamA (TP0326) and Localization of Rare Outer Membrane Proteins
  8. Altmetric Badge
    Chapter 7 Analyzing the Role of Periplasmic Folding Factors in the Biogenesis of OMPs and Members of the Type V Secretion System
  9. Altmetric Badge
    Chapter 8 An In Vitro Assay for Substrate Translocation by FhaC in Liposomes
  10. Altmetric Badge
    Chapter 9 Measuring Cell–Cell Binding Using Flow-Cytometry
  11. Altmetric Badge
    Chapter 10 Methods to Characterize Folding and Function of BamA Cross-Link Mutants
  12. Altmetric Badge
    Chapter 11 The BAM Complex
  13. Altmetric Badge
    Chapter 12 Assessing the Outer Membrane Insertion and Folding of Multimeric Transmembrane β-Barrel Proteins
  14. Altmetric Badge
    Chapter 13 The Expression, Purification, and Structure Determination of BamA from E. coli
  15. Altmetric Badge
    Chapter 14 Expression and Purification of the Individual Bam Components BamB–E
  16. Altmetric Badge
    Chapter 15 Structure Determination of the BAM Complex Accessory Lipoproteins BamB–E
  17. Altmetric Badge
    Chapter 16 An In Vitro Assay for Outer Membrane Protein Assembly by the BAM Complex
  18. Altmetric Badge
    Chapter 17 Identification of BamC on the Surface of E. coli
  19. Altmetric Badge
    Chapter 18 The BAM Complex
  20. Altmetric Badge
    Chapter 19 Expression, Purification, and Screening of BamE, a Component of the BAM Complex, for Structural Characterization
  21. Altmetric Badge
    Chapter 20 Purification and Bicelle Crystallization for Structure Determination of the E. coli Outer Membrane Protein TamA
  22. Altmetric Badge
    Chapter 21 Strategies for the Analysis of Bam Recognition Motifs in Outer Membrane Proteins
  23. Altmetric Badge
    Chapter 22 Summary and Future Directions
  24. Altmetric Badge
    Chapter 23 Erratum to: The Role of a Destabilized Membrane for OMP Insertion
Attention for Chapter 8: An In Vitro Assay for Substrate Translocation by FhaC in Liposomes
Altmetric Badge

Citations

dimensions_citation
3 Dimensions

Readers on

mendeley
1 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
An In Vitro Assay for Substrate Translocation by FhaC in Liposomes
Chapter number 8
Book title
The BAM Complex
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2871-2_8
Pubmed ID
Book ISBNs
978-1-4939-2870-5, 978-1-4939-2871-2
Authors

Enguo Fan, Derrick Norell, Matthias Müller, Fan, Enguo, Norell, Derrick, Müller, Matthias

Abstract

The two-partner secretion (TPS) pathway is used by gram-negative bacteria to secrete a large family of virulence exoproteins. Its name is derived from the fact that it involves two proteins, a secreted TpsA protein and a cognate TpsB transporter in the outer membrane. A typical TPS system is represented by the filamentous hemagglutinin FhaB (TpsA protein) and its transporter FhaC (TpsB protein) of Bordetella pertussis. Results from mutational analysis and heterologous expression experiments suggested that FhaC is essential for FhaB translocation across the outer membrane of bacteria. We have devised a cell-free biochemical assay to reconstitute in vitro the translocation of FhaB into reconstituted membrane vesicles. Thereby the clearest evidence has been provided that the single β-barrel FhaC protein serves as the sole translocator to transport FhaB across the outer membrane. This is the first in vitro assay for protein secretion across the Escherichia coli outer membrane and the detailed protocol described here should be amenable to modifications and application to the analysis of related protein transport events occurring at the outer membranes of gram-negative bacteria.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 1 Mendeley reader of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 100%
Readers by discipline Count As %
Unspecified 1 100%