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来自蝶豆(Clitoria ternatea)的免疫刺激和革兰氏阴性特异性抗菌环肽。

Immunostimulating and Gram-negative-specific antibacterial cyclotides from the butterfly pea (Clitoria ternatea).

作者信息

Nguyen Kim Ngan T, Nguyen Giang Kien Truc, Nguyen Phuong Quoc Thuc, Ang Koon Hwee, Dedon Peter C, Tam James P

机构信息

School of Biological Sciences, Nanyang Technological University, Singapore City, Singapore.

Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

出版信息

FEBS J. 2016 Jun;283(11):2067-90. doi: 10.1111/febs.13720. Epub 2016 Apr 20.

Abstract

UNLABELLED

Cyclotides are plant-derived, cyclic miniproteins with three interlocking disulfide bonds that have attracted great interests because of their excellent stability and potential as peptide therapeutics. In this study, we characterize the cyclotides of the medicinal plant Clitoria ternatea (butterfly pea) and investigate their biological activities. Using a combined proteomic and transcriptomic method, we identified 41 novel cyclotide sequences, which we named cliotides, making C. ternatea one of the richest cyclotide-producing plants to date. Selected members of the cationic cliotides display potent antibacterial activity specifically against Gram-negative bacteria with minimal inhibitory concentrations as low as 0.5 μm. Remarkably, they also possess prominent immunostimulating activity. At a concentration of 1 μm, cationic cliotides are capable of augmenting the secretion of various cytokines and chemokines in human monocytes at both resting and lipopolysaccharide-stimulated states. Chemokines such as macrophage inflammatory proteins 1α and 1β, interferon γ-induced protein 10, interleukin 8 and tumor necrosis factor α were among the most upregulated with up to 129-fold increase in secretion level. These findings suggest cyclotides can serve as potential candidates for novel immunomodulating therapeutics.

DATABASE

The protein sequences reported in this paper (cT13-cT21) are available in the UniProt Knowledgebase under the accession numbers C0HJS0, C0HJS1, C0HJS2, C0HJS3, C0HJS4, C0HJS5, C0HJS6, C0HJS7 and C0HJS8, respectively. The transcriptome data in this paper are available at the Sequence Read Archive database (NCBI) under accession number SRR1613316. The protein precursors reported in this paper (ctc13, ctc15, ctc17-ctc19, ctc21-ctc53) are available at GenBank under the accession numbers KT732712, KT732713, KT732714, KT732715, KT732716, KT732717, KT732718, KT732719, KT732720, KT732721, KT732722, KT732723, KT732724, KT732725, KT732726, KT732727, KT732728, KT732729, KT732730, KT732731, KT732732, KT732733, KT732734, KT732735, KT732736, KT732737, KT732738, KT732739, KT732740, KT732741, KT732742, KT732743, KT732744, KT732745, KT732746, KT732747, KT732748 and KT732749, respectively.

摘要

未标记

环肽是植物来源的环状小蛋白,具有三个相互锁定的二硫键,因其出色的稳定性和作为肽类药物的潜力而备受关注。在本研究中,我们对药用植物蝶豆的环肽进行了表征,并研究了它们的生物活性。通过蛋白质组学和转录组学相结合的方法,我们鉴定出41个新的环肽序列,将其命名为cliotides,使蝶豆成为迄今为止环肽产量最丰富的植物之一。阳离子cliotides的选定成员对革兰氏阴性菌表现出强大的抗菌活性,最低抑菌浓度低至0.5μm。值得注意的是,它们还具有显著的免疫刺激活性。在浓度为1μm时,阳离子cliotides能够在静息和脂多糖刺激状态下增强人单核细胞中各种细胞因子和趋化因子的分泌。巨噬细胞炎性蛋白1α和1β、干扰素γ诱导蛋白10、白细胞介素8和肿瘤坏死因子α等趋化因子的分泌上调最为明显,分泌水平最高可增加129倍。这些发现表明环肽可作为新型免疫调节疗法的潜在候选物。

数据库

本文报道的蛋白质序列(cT13 - cT21)可在UniProt知识库中获取,登录号分别为C0HJS0、C0HJS1、C0HJS2、C0HJS3、C0HJS4、C0HJS5、C0HJS6、C0HJS7和C0HJS8。本文的转录组数据可在序列读取存档数据库(NCBI)中获取,登录号为SRR1613316。本文报道的蛋白质前体(ctc13、ctc15、ctc17 - ctc19、ctc21 - ctc53)可在GenBank中获取,登录号分别为KT732712、KT732,713、KT732714、KT732715、KT732716、KT732717、KT732718、KT732719、KT732720,KT732721、KT732722、KT732723、KT732724、KT732725、KT732726、KT732727、KT732728、KT732729、KT732730、KT732731、KT732732、KT732733、KT732734、KT732735、KT732736、KT732737、KT732738、KT732739、KT732740、KT732741、KT732742、KT732743、KT732744、KT732745、KT732746、KT732747、KT732748和KT732749。

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