Cellular Entry of Binary and Pore-Forming Bacterial Toxins
Bridging cellular membranes is a key step in the pathogenic action of both binary and pore-forming bacterial toxins. The former use their translocation domains, containing various structural motifs, to ensure efficient delivery of the toxic component into the host cell, while the latter act on the c...
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| Format: | Book Chapter |
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MDPI - Multidisciplinary Digital Publishing Institute
2018
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| Online Access: | Get Fullteks DOAB: description of the publication |
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| LEADER | 02293naaaa2200313uu 4500 | ||
|---|---|---|---|
| 001 | doab_20_500_12854_42868 | ||
| 005 | 20210211 | ||
| 020 | |a books978-3-03842-703-2 | ||
| 020 | |a 9783038427032 | ||
| 020 | |a 9783038427049 | ||
| 024 | 7 | |a 10.3390/books978-3-03842-703-2 |c doi | |
| 041 | 0 | |a English | |
| 042 | |a dc | ||
| 100 | 1 | |a Alexey S. Ladokhin (Ed.) |4 auth | |
| 245 | 1 | 0 | |a Cellular Entry of Binary and Pore-Forming Bacterial Toxins |
| 260 | |b MDPI - Multidisciplinary Digital Publishing Institute |c 2018 | ||
| 300 | |a 1 electronic resource (128 p.) | ||
| 506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
| 520 | |a Bridging cellular membranes is a key step in the pathogenic action of both binary and pore-forming bacterial toxins. The former use their translocation domains, containing various structural motifs, to ensure efficient delivery of the toxic component into the host cell, while the latter act on the cellular membrane itself. In either case, the integrity of the membrane is compromised via targeted protein-lipid and protein-protein interactions triggered by specific signals, such as proteolytic cleavage or endosomal acidification. This Special Issue presents recent advances in characterizing functional, structural and thermodynamic aspects of the conformational switching and membrane interactions involved in the cellular entry of bacterial protein toxins. Deciphering the physicochemical principles underlying these processes is also a prerequisite for the use of protein engineering to develop toxin-based molecular vehicles capable of targeted delivery of therapeutic agents to tumors and other diseased tissues. | ||
| 540 | |a Creative Commons |f https://creativecommons.org/licenses/by-nc-nd/4.0/ |2 cc |4 https://creativecommons.org/licenses/by-nc-nd/4.0/ | ||
| 546 | |a English | ||
| 653 | |a membrane permeabilization and translocation | ||
| 653 | |a toxin-membrane interactions | ||
| 653 | |a bacterial protein toxins | ||
| 653 | |a conformational switching | ||
| 653 | |a toxin-based targeted delivery of therapeutic agents | ||
| 653 | |a cellular uptake | ||
| 856 | 4 | 0 | |a www.oapen.org |u http://www.mdpi.com/books/pdfview/book/531 |7 0 |z Get Fullteks |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/42868 |7 0 |z DOAB: description of the publication |