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首页> 外文期刊>The Journal of Antibiotics: An International Journal >Formatio of Anion-selective Membrane Pores by Texenomycin A, A Basic Lipopeptaibol Antibiotic
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Formatio of Anion-selective Membrane Pores by Texenomycin A, A Basic Lipopeptaibol Antibiotic

机译:碱性脂环素抗生素Texenomycin A对阴离子选择性膜孔的形成

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摘要

Peptaibols are fungal linear peptides that own their biological activities to the formation of ion-penetrable pores within biological membranes. Our previous investigations suggested that the constituting amino acids determine channel stability, ion selectivity and biological activities. Lipopeptaibol antibiotics such as texenomycin A (1, fig. 1) are distinguishable from the common peptaibols due to acylation of the N-terminus by a long-chain fatty acid and substitution of the carbon terminus by amino or guanidino moieties.
机译:肽醇是真菌线性肽,其具有其生物活性以在生物膜内形成可离子渗透的孔。我们以前的研究表明,组成氨基酸决定通道稳定性,离子选择性和生物活性。脂肽醇抗生素,如特松霉素A(图1),与普通的肽醇区分开来,这是由于N端被长链脂肪酸酰化并碳端被氨基或胍基部分取代。

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