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Channel-Forming Bacterial Toxins in Biosensing and Macromolecule Delivery
Authors:Philip A. Gurnev  Ekaterina M. Nestorovich
Affiliation:1.Physics Department, University of Massachusetts, Amherst, MA 01003, USA; E-Mail: ;2.Program in Physical Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20008, USA;3.Department of Biology, the Catholic University of America, Washington, DC 20064, USA
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.
Keywords:gramicidin A, α  -hemolysin, anthrax toxin, biosensing, stochastic sensing, ion channel, biological nanopore, protein translocation, targeted toxins, drug delivery, polymer transport
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