2007
DOI: 10.1016/j.intimp.2007.01.006
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Shrimp (Penaeus monodon) anti-lipopolysaccharide factor reduces the lethality of Pseudomonas aeruginosa sepsis in mice

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Cited by 41 publications
(25 citation statements)
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References 45 publications
(58 reference statements)
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“…The amino acid sequence of cSALF is ECKFTVKPYLKRFQ-VYYKGRMWCP [29]. It exhibits antimicrobial ability against both Gram-positive and -negative bacteria and is able to form an amphipathic hairpin loop in the region of 20e21 amino acids in helical length, which can form an LPS-binding motif, or disrupt viral functions at the phospholipid membrane bilayer [29].…”
Section: Discussionmentioning
confidence: 99%
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“…The amino acid sequence of cSALF is ECKFTVKPYLKRFQ-VYYKGRMWCP [29]. It exhibits antimicrobial ability against both Gram-positive and -negative bacteria and is able to form an amphipathic hairpin loop in the region of 20e21 amino acids in helical length, which can form an LPS-binding motif, or disrupt viral functions at the phospholipid membrane bilayer [29].…”
Section: Discussionmentioning
confidence: 99%
“…It exhibits antimicrobial ability against both Gram-positive and -negative bacteria and is able to form an amphipathic hairpin loop in the region of 20e21 amino acids in helical length, which can form an LPS-binding motif, or disrupt viral functions at the phospholipid membrane bilayer [29]. However, NNV is non-enveloped, and the anti-NNV mechanism of cSALF was achieved by agglutinating NNV capsid protein, similar to that of TH 1-5, and the agglutination was irreversible, indicating that the two peptides might change NNV virion or capsid protein from hydrophilic to hydrophobic, causing the formation of aggregates.…”
Section: Discussionmentioning
confidence: 99%
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“…Parallel to this, the peptides were able to reduce the bacteria-induced produc tion of TNF-α in the animals. However, already at a concentration of 2 μg/ml the peptides exhibited significant cytotoxicity in HeLa, MCF-7, and HT1080 cell lines, impeding their use as an anti-infective drug [31].…”
Section: Development and Anti-lps Eff Ects Of Synthetic Antimicrobialmentioning
confidence: 99%
“…Functional characterization of ALFs has been conducted by chemically synthesizing the LPS domain region, [16][17][18][19][20][21][22] and by recombinant expression of mature peptides. 9,13,[23][24][25][26][27][28] Biological activity reported so far for ALFs include antibacterial, 6,9,20 antifungal, 6,27 antiviral, 29,30 immunomodulatory, 31 antitumor, 32 anti-inflammatory, and antiprotozoal activity. 32,33 As per the previous studies, the structure of ALF was elucidated using nuclear magnetic resonance (NMR) spectroscopy, with the finding that it was composed of three α-helices packed against a four-stranded β-sheet.…”
Section: Introductionmentioning
confidence: 99%