Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Colicin U from Shigella boydii Forms Voltage-Dependent Pores

T. Dolejšová, A. Sokol, J. Bosák, D. Šmajs, I. Konopásek, G. Mikušová, R. Fišer,

. 2019 ; 201 (24) : . [pub] 20191120

Language English Country United States

Document type Journal Article, Research Support, Non-U.S. Gov't

E-resources Online Full text

NLK Free Medical Journals from 1916 to 6 months ago
Freely Accessible Science Journals from 1916 to 6 months ago
PubMed Central from 1916 to 1 year ago
Europe PubMed Central from 1916 to 6 months ago
Open Access Digital Library from 1916-01-01
Open Access Digital Library from 1916-01-01

Colicin U is a protein produced by the bacterium Shigella boydii (serovars 1 and 8). It exerts antibacterial activity against strains of the enterobacterial genera Shigella and Escherichia Here, we report that colicin U forms voltage-dependent pores in planar lipid membranes; its single-pore conductance was found to be about 22 pS in 1 M KCl at pH 6 under 80 mV in asolectin bilayers. In agreement with the high degree of homology between their C-terminal domains, colicin U shares some pore characteristics with the related colicins A and B. Colicin U pores are strongly pH dependent, and as we deduced from the activity of colicin U in planar membranes at different protein concentrations, they have a monomeric pore structure. However, in contrast to related colicins, we observed a very low cationic selectivity of colicin U pores (1.5/1 of K+/Cl- at pH 6) along with their atypical voltage gating. Finally, using nonelectrolytes, we determined the inner diameter of the pores to be in the range of 0.7 to 1 nm, which is similar to colicin Ia, but with a considerably different inner profile.IMPORTANCE Currently, a dramatic increase in antibiotic resistance is driving researchers to find new antimicrobial agents. The large group of toxins called bacteriocins appears to be very promising from this point of view, especially because their narrow killing spectrum allows specific targeting against selected bacterial strains. Colicins are a subgroup of bacteriocins that act on Gram-negative bacteria. To date, some colicins are commercially used for the treatment of animals (1) and tested as a component of engineered species-specific antimicrobial peptides, which are studied for the potential treatment of humans (2). Here, we present a thorough single-molecule study of colicin U which leads to a better understanding of its mode of action. It extends the range of characterized colicins available for possible future medical applications.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc20023474
003      
CZ-PrNML
005      
20201214130131.0
007      
ta
008      
201125s2019 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1128/JB.00493-19 $2 doi
035    __
$a (PubMed)31548276
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Dolejšová, Tereza $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic.
245    10
$a Colicin U from Shigella boydii Forms Voltage-Dependent Pores / $c T. Dolejšová, A. Sokol, J. Bosák, D. Šmajs, I. Konopásek, G. Mikušová, R. Fišer,
520    9_
$a Colicin U is a protein produced by the bacterium Shigella boydii (serovars 1 and 8). It exerts antibacterial activity against strains of the enterobacterial genera Shigella and Escherichia Here, we report that colicin U forms voltage-dependent pores in planar lipid membranes; its single-pore conductance was found to be about 22 pS in 1 M KCl at pH 6 under 80 mV in asolectin bilayers. In agreement with the high degree of homology between their C-terminal domains, colicin U shares some pore characteristics with the related colicins A and B. Colicin U pores are strongly pH dependent, and as we deduced from the activity of colicin U in planar membranes at different protein concentrations, they have a monomeric pore structure. However, in contrast to related colicins, we observed a very low cationic selectivity of colicin U pores (1.5/1 of K+/Cl- at pH 6) along with their atypical voltage gating. Finally, using nonelectrolytes, we determined the inner diameter of the pores to be in the range of 0.7 to 1 nm, which is similar to colicin Ia, but with a considerably different inner profile.IMPORTANCE Currently, a dramatic increase in antibiotic resistance is driving researchers to find new antimicrobial agents. The large group of toxins called bacteriocins appears to be very promising from this point of view, especially because their narrow killing spectrum allows specific targeting against selected bacterial strains. Colicins are a subgroup of bacteriocins that act on Gram-negative bacteria. To date, some colicins are commercially used for the treatment of animals (1) and tested as a component of engineered species-specific antimicrobial peptides, which are studied for the potential treatment of humans (2). Here, we present a thorough single-molecule study of colicin U which leads to a better understanding of its mode of action. It extends the range of characterized colicins available for possible future medical applications.
650    _2
$a buněčná membrána $x metabolismus $7 D002462
650    _2
$a koliciny $x metabolismus $7 D003087
650    _2
$a koncentrace vodíkových iontů $7 D006863
650    _2
$a gating iontového kanálu $7 D015640
650    _2
$a lipidové dvojvrstvy $x metabolismus $7 D008051
650    _2
$a permeabilita $7 D010539
650    _2
$a chlorid draselný $x farmakologie $7 D011189
650    _2
$a Shigella boydii $x metabolismus $7 D012761
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Sokol, Albert $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic.
700    1_
$a Bosák, Juraj $u Department of Biology, Faculty of Medicine, Masaryk University, Kamenice, Brno, Czech Republic.
700    1_
$a Šmajs, David $u Department of Biology, Faculty of Medicine, Masaryk University, Kamenice, Brno, Czech Republic.
700    1_
$a Konopásek, Ivo $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic.
700    1_
$a Mikušová, Gabriela $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic.
700    1_
$a Fišer, Radovan $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic fiserr@natur.cuni.cz.
773    0_
$w MED00002537 $t Journal of bacteriology $x 1098-5530 $g Roč. 201, č. 24 (2019)
856    41
$u https://pubmed.ncbi.nlm.nih.gov/31548276 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20201125 $b ABA008
991    __
$a 20201214130130 $b ABA008
999    __
$a ok $b bmc $g 1595793 $s 1114150
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2019 $b 201 $c 24 $e 20191120 $i 1098-5530 $m Journal of bacteriology $n J Bacteriol $x MED00002537
LZP    __
$a Pubmed-20201125

Find record

Citation metrics

Logged in users only

Archiving options

Loading data ...