A Technology for Developing Synbodies with Antibacterial Activity

被引:17
|
作者
Domenyuk, Valeriy [1 ]
Loskutov, Andrey [1 ]
Johnston, Stephen Albert [1 ,2 ]
Diehnelt, Chris W. [1 ]
机构
[1] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
[2] Arizona State Univ, Sch Life Sci, Tempe, AZ USA
来源
PLOS ONE | 2013年 / 8卷 / 01期
关键词
HOST-DEFENSE PEPTIDES; ANTIMICROBIAL PEPTIDES; STAPHYLOCOCCUS-AUREUS; ANTIBIOTICS; SELECTIVITY; SEQUENCE; DESIGN;
D O I
10.1371/journal.pone.0054162
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The rise in antibiotic resistance has led to an increased research focus on discovery of new antibacterial candidates. While broad-spectrum antibiotics are widely pursued, there is evidence that resistance arises in part from the wide spread use of these antibiotics. Our group has developed a system to produce protein affinity agents, called synbodies, which have high affinity and specificity for their target. In this report, we describe the adaptation of this system to produce new antibacterial candidates towards a target bacterium. The system functions by screening target bacteria against an array of 10,000 random sequence peptides and, using a combination of membrane labeling and intracellular dyes, we identified peptides with target specific binding or killing functions. Binding and lytic peptides were identified in this manner and in vitro tests confirmed the activity of the lead peptides. A peptide with antibacterial activity was linked to a peptide specifically binding Staphylococcus aureus to create a synbody with increased antibacterial activity. Subsequent tests showed that this peptide could block S. aureus induced killing of HEK293 cells in a co-culture experiment. These results demonstrate the feasibility of using the synbody system to discover new antibacterial candidate agents.
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页数:11
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