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本文引用的文献

1
Ultrashort peptide bioconjugates are exclusively antifungal agents and synergize with cyclodextrin and amphotericin B.超短肽生物缀合物是专门的抗真菌药物,与环糊精和两性霉素 B 具有协同作用。
Antimicrob Agents Chemother. 2012 Jan;56(1):1-9. doi: 10.1128/AAC.00468-11. Epub 2011 Oct 17.
2
Easy strategy to increase salt resistance of antimicrobial peptides.提高抗菌肽耐盐性的简易策略。
Antimicrob Agents Chemother. 2011 Oct;55(10):4918-21. doi: 10.1128/AAC.00202-11. Epub 2011 Jul 18.
3
Rational design of tryptophan-rich antimicrobial peptides with enhanced antimicrobial activities and specificities.具有增强的抗菌活性和特异性的富含色氨酸的抗菌肽的合理设计。
Chembiochem. 2010 Nov 2;11(16):2273-82. doi: 10.1002/cbic.201000372.
4
Effect of the hydrophobicity to net positive charge ratio on antibacterial and anti-endotoxin activities of structurally similar antimicrobial peptides.结构相似的抗菌肽的疏水性与净正电荷比对抗菌和抗内毒素活性的影响。
Biochemistry. 2010 Feb 9;49(5):853-61. doi: 10.1021/bi900724x.
5
Increased potency of a novel D-beta-naphthylalanine-substituted antimicrobial peptide against fluconazole-resistant fungal pathogens.一种新型D-β-萘丙氨酸取代的抗菌肽对氟康唑耐药真菌病原体的效力增强。
FEMS Yeast Res. 2009 Sep;9(6):967-70. doi: 10.1111/j.1567-1364.2009.00531.x. Epub 2009 May 21.
6
Boosting antimicrobial peptides by hydrophobic oligopeptide end tags.通过疏水性寡肽末端标签增强抗菌肽。
J Biol Chem. 2009 Jun 26;284(26):17584-94. doi: 10.1074/jbc.M109.011650. Epub 2009 Apr 27.
7
End-tagging of ultra-short antimicrobial peptides by W/F stretches to facilitate bacterial killing.通过W/F延伸对超短抗菌肽进行末端标记以促进细菌杀伤。
PLoS One. 2009;4(4):e5285. doi: 10.1371/journal.pone.0005285. Epub 2009 Apr 17.
8
Tryptophan end-tagging of antimicrobial peptides for increased potency against Pseudomonas aeruginosa.用于增强抗铜绿假单胞菌效力的抗菌肽色氨酸末端标记
Biochim Biophys Acta. 2009 Aug;1790(8):800-8. doi: 10.1016/j.bbagen.2009.03.029. Epub 2009 Apr 5.
9
Antibacterial activity of ultrashort cationic lipo-beta-peptides.超短阳离子脂肽的抗菌活性
Antimicrob Agents Chemother. 2009 May;53(5):2215-7. doi: 10.1128/AAC.01100-08. Epub 2009 Feb 23.
10
Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies.抗菌肽和宿主防御肽作为新型抗感染治疗策略。
Nat Biotechnol. 2006 Dec;24(12):1551-7. doi: 10.1038/nbt1267.

提高短抗菌肽的耐盐性。

Boosting salt resistance of short antimicrobial peptides.

机构信息

Institute of Biotechnology and Department of Medical Science, National Tsing Hua University, Hsinchu, Taiwan.

出版信息

Antimicrob Agents Chemother. 2013 Aug;57(8):4050-2. doi: 10.1128/AAC.00252-13. Epub 2013 May 28.

DOI:10.1128/AAC.00252-13
PMID:23716061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3719776/
Abstract

The efficacies of many antimicrobial peptides are greatly reduced under high salt concentrations, therefore limiting their use as pharmaceutical agents. Here, we describe a strategy to boost salt resistance and serum stability of short antimicrobial peptides by adding the nonnatural bulky amino acid β-naphthylalanine to their termini. The activities of the short salt-sensitive tryptophan-rich peptide S1 were diminished at high salt concentrations, whereas the activities of its β-naphthylalanine end-tagged variants were less affected.

摘要

许多抗菌肽在高盐浓度下的功效大大降低,因此限制了它们作为药物的应用。在这里,我们描述了一种通过在其末端添加非天然大体积氨基酸β-萘丙氨酸来提高短抗菌肽的耐盐性和血清稳定性的策略。富含色氨酸的短盐敏感肽 S1 的活性在高盐浓度下减弱,而其β-萘丙氨酸末端标记变体的活性受影响较小。