Effects of arginine and leucine substitutions on anti-endotoxic activities and mechanisms of action of cationic and amphipathic antimicrobial octadecapeptide from rice α -amylase

Author:

Taniguchi Masayuki12,Ochiai Akihito1,Toyoda Ryu1,Sato Teppei1,Saitoh Eiichi3,Kato Tetsuo4,Tanaka Takaaki1

Affiliation:

1. Department of Materials Science and Technology, Graduate School of Science and Technology; Niigata University; Niigata 950-2181 Japan

2. Center for Transdisciplinary Research; Niigata University; Niigata 950-2181 Japan

3. Graduate School of Technology; Niigata Institute of Technology; Niigata 945-1195 Japan

4. Department of Chemistry; Tokyo Dental College; Tokyo 101-0062 Japan

Publisher

Wiley

Subject

Organic Chemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry,Structural Biology

Reference48 articles.

1. De novo designed lipopolysaccharide binding peptides: structure based development of antiendotoxic and antimicrobial drugs;Bhattacharjya;Curr. Med. Chem.,2010

2. Structure and function of a potent lipopolysaccharide-binding antimicrobial and anti-inflammatory peptide;Wei;J. Med. Chem.,2013

3. A novel peptide derived from human pancreatitis-associated protein inhibits inflammation in vitro and in vivo and blocks NF-kappa B signaling pathway;Yang;PLoS One,2011

4. Augmentation of lipopolysaccharide-neutralizing activities of human cathelicidin CAP18/LL37-derived from antimicrobial peptides by replacement with hydrophobic and cationic amino acid residues;Nagaoka;Clin. Diagn. Lab. Immunol.,2002

5. Prokaryotic selectivity and LPS-neutralizing activity of short antimicrobial peptides designed from the human antimicrobial peptide LL-37;Nan;Peptides,2012

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