Division of Pharmacognosy, Department of Medicinal Chemistry, Biomedical Center, Uppsala University , Box 574, SE-751 23 Uppsala, Sweden.
Department of Chemistry, Materials and Surfaces, SP Technical Research Institute of Sweden , Arvid Wallgrens Backe 20, SE-413 46 Göteborg, Sweden.
J Nat Prod. 2015 Aug 28;78(8):1886-93. doi: 10.1021/acs.jnatprod.5b00210. Epub 2015 Jul 29.
Two disulfide-containing peptides, barrettides A (1) and B (2), from the cold-water marine sponge Geodia barretti are described. Those 31 amino acid residue long peptides were sequenced using mass spectrometry methods and structurally characterized using NMR spectroscopy. The structure of 1 was confirmed by total synthesis using the solid-phase peptide synthesis approach that was developed. The two peptides were found to differ only at a single position in their sequence. The three-dimensional structure of 1 revealed that these peptides possess a unique fold consisting of a long β-hairpin structure that is cross-braced by two disulfide bonds in a ladder-like arrangement. The peptides are amphipathic in nature with the hydrophobic and charged residues clustered on separate faces of the molecule. The barrettides were found not to inhibit the growth of either Escherichia coli or Staphylococcus aureus but displayed antifouling activity against barnacle larvae (Balanus improvisus) without lethal effects in the concentrations tested.
两种含二硫键的肽,barrettides A(1)和 B(2),来自冷水海洋海绵 Geodia barretti。这些 31 个氨基酸残基长的肽是通过质谱方法测序,并通过 NMR 光谱学结构表征。1 的结构通过使用固相肽合成方法的全合成来证实,该方法是开发的。这两种肽在其序列中仅在一个位置上有所不同。1 的三维结构表明,这些肽具有独特的折叠结构,由一个长的β-发夹结构组成,该结构由两个二硫键以梯状排列交叉支撑。这些肽具有两亲性,疏水性和带电残基聚集在分子的不同面上。barrettides 被发现既不抑制大肠杆菌或金黄色葡萄球菌的生长,也不显示对藤壶幼虫(Balanus improvisus)的抗污活性,但在测试浓度下没有致命影响。