4.6 Review Book Chapter

Border Crossings: Colicins and Transporters

Journal

ANNUAL REVIEW OF GENETICS, VOL 46
Volume 46, Issue -, Pages 209-231

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-genet-110711-155427

Keywords

outer membrane receptor; outer membrane translocator

Funding

  1. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI091633] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM018457] Funding Source: NIH RePORTER
  3. NIAID NIH HHS [R01 AI091633, R01AI091633] Funding Source: Medline
  4. NIGMS NIH HHS [R01-GM018457] Funding Source: Medline

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Colicins are protein toxins produced by Escherichia coli to kill related bacteria. They must cross the target cell outer membrane (OM), and some must also cross the inner membrane (IM). To accomplish cellular import, colicins have parasitized E. coli nutrient transporters as well as IM and periplasmic proteins normally used to maintain cell wall integrity or provide energy for nutrient uptake through transporters. Colicins have evolved to use both transporters and other membrane proteins through mechanisms different from those employed in physiological substrate uptake. Extended receptor-binding domains allow some colicins to search by lateral diffusion for binding sites on their OM translocators while bound to their primary OM receptor. Transport across the OM is initiated by entry of the unstructured N-terminal translocation domain into the translocator. Periplasmic and IM networks subsequently accomplish insertion of the colicin cytotoxic domain into or across the IM.

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