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Related Concept Videos

Gram-negative Bacterial Protein Secretion Systems01:17

Gram-negative Bacterial Protein Secretion Systems

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Gram-negative bacteria utilize sophisticated protein secretion systems to transport proteins across their double-membrane envelope into the extracellular environment or host cells. Based on their mechanism of action, these systems are classified into one-step and two-step pathways.One-Step Secretion Systems (Types I, III, IV, and VI)One-step secretion systems bypass the periplasm entirely, forming a continuous channel that spans both the inner and outer membranes:Type I Secretion System (T1SS):...
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Bacterial Translocation and Protein Secretion01:26

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Bacterial protein secretion involves translocation systems to ensure proteins reach their designated locations, including the plasma membrane, periplasm, outer membrane, or the external environment. These translocation systems are vital for bacterial physiology, supporting processes like membrane assembly, enzymatic activity in the periplasm, and interactions with the external environment. The division of labor between Sec and Tat pathways ensures efficiency in handling proteins with diverse...
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Nuclear encoded mitochondrial precursors are imported to the inner membrane in a multistep process involving two separate translocons, TIM22 and TIM23. TIM23 is a cation-selective pore that remains closed by the N terminal segment of the protein. Negative charges on the TIM23 act as a receptor for the incoming precursor, pulling the positively charged matrix-targeting sequence for peptide insertion and translocation.
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ABC Transporters: Importer01:27

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ATP-binding cassette or ABC transporters are a class of ATP-driven pumps that hydrolyze ATP to move solutes across the membrane. They can be grouped into importers and exporters. While exporters are present in all domains of life, importers exist only in bacteria and some plants.
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Integral membrane proteins are proteins adhered to the lipid bilayer of a cell organelle or membrane. They can be of two types: transmembrane integral proteins that span the lipid bilayer and monotopic proteins that are attached to either side of the membrane but do not pass through it.
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The rough ER membrane synthesizes, assembles, and embeds transmembrane proteins in diverse topologies. These proteins function as transporters or channels and can remain in the ER membrane or are sent to the Golgi complex, lysosome, and cell membrane.
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Transmembrane substrates of type three secretion system injectisomes.

Camilla Godlee1,2, David W Holden1

  • 1MRC Centre for Molecular Bacteriology and Infection, Imperial College London, Armstrong Road, London SW7 2AZ, UK.

Microbiology (Reading, England)
|February 7, 2023
PubMed
Summary

Gram-negative bacteria use a type three secretion system injectisome to deliver virulence effectors into host cells. This review details how these bacterial proteins integrate into host membranes and their functions.

Keywords:
effectorinjectisomemembrane integrationtranslocontype three secretion system

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Area of Science:

  • Microbiology
  • Cell Biology
  • Pathogenesis

Background:

  • Gram-negative bacterial pathogens utilize the type three secretion system (T3SS) injectisome to translocate effector proteins into host cells.
  • These effectors are crucial for bacterial invasion, replication, immune evasion, and transmission.

Approach:

  • This review focuses on transmembrane translocon proteins and effectors secreted by the injectisome.
  • It examines the mechanisms of their integration into host cell membranes and the functional consequences of their localization.

Key Points:

  • The injectisome forms a pore in the host cell membrane for effector delivery.
  • Some effectors integrate into host membranes, performing unique biochemical functions.
  • Both translocon proteins and transmembrane effectors avoid aggregation and improper localization within the bacterial cell.

Conclusions:

  • Understanding the membrane integration of bacterial effectors is key to comprehending host-pathogen interactions.
  • The localization of injectisome effectors within host membranes confers specific functional advantages for bacterial pathogens.