AI Article Synopsis

  • Pore-forming bacterial toxins facilitate the movement of various substances across cell membranes, and recent research has advanced understanding of how these channels work.
  • Advances in techniques like single-channel electrical recordings and X-ray crystallography have expanded knowledge of molecular transport, paving the way for applications in nanobiotechnology.
  • The article reviews the use of different bacterial toxins in detecting molecules, cancer therapies, and drug delivery, focusing on specific toxins and their innovative applications in medicine and technology.

Article Abstract

To intoxicate cells, pore-forming bacterial toxins are evolved to allow for the transmembrane traffic of different substrates, ranging from small inorganic ions to cell-specific polypeptides. Recent developments in single-channel electrical recordings, X-ray crystallography, protein engineering, and computational methods have generated a large body of knowledge about the basic principles of channel-mediated molecular transport. These discoveries provide a robust framework for expansion of the described principles and methods toward use of biological nanopores in the growing field of nanobiotechnology. This article, written for a special volume on "Intracellular Traffic and Transport of Bacterial Protein Toxins", reviews the current state of applications of pore-forming bacterial toxins in small- and macromolecule-sensing, targeted cancer therapy, and drug delivery. We discuss the electrophysiological studies that explore molecular details of channel-facilitated protein and polymer transport across cellular membranes using both natural and foreign substrates. The review focuses on the structurally and functionally different bacterial toxins: gramicidin A of Bacillus brevis, α-hemolysin of Staphylococcus aureus, and binary toxin of Bacillus anthracis, which have found their "second life" in a variety of developing medical and technological applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147595PMC
http://dx.doi.org/10.3390/toxins6082483DOI Listing

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