Twin-Arginine Protein Translocation

Curr Top Microbiol Immunol. 2017:404:69-94. doi: 10.1007/82_2016_7.

Abstract

Twin-arginine protein translocation systems (Tat) translocate fully folded and co-factor-containing proteins across biological membranes. In this review, we focus on the Tat pathway of Gram-positive bacteria. The minimal Tat pathway is composed of two components, namely a TatA and TatC pair, which are often complemented with additional TatA-like proteins. We provide overviews of our current understanding of Tat pathway composition and mechanistic aspects related to Tat-dependent cargo protein translocation. This includes Tat pathway flexibility, requirements for the correct folding and incorporation of co-factors in cargo proteins and the functions of known cargo proteins. Tat pathways of several Gram-positive bacteria are discussed in detail, with emphasis on the Tat pathway of Bacillus subtilis. We discuss both shared and unique features of the different Gram-positive bacterial Tat pathways. Lastly, we highlight topics for future research on Tat, including the development of this protein transport pathway for the biotechnological secretion of high-value proteins and its potential applicability as an antimicrobial drug target in pathogens.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / physiology*
  • Escherichia coli Proteins / physiology
  • Gram-Positive Bacteria / metabolism*
  • Membrane Transport Proteins / physiology*
  • Protein Folding
  • Protein Transport

Substances

  • Bacterial Proteins
  • Escherichia coli Proteins
  • Membrane Transport Proteins
  • TatA protein, E coli
  • TatC protein, E coli