Membrane lipid composition directs the cellular selectivity of antimicrobial metallohelices.

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nicola J Rogers, Miles L Postings, Ann M Dixon, John Moat, Georgia Shreeve, Louise Stuart, Nicholas R Waterfield, Peter Scott
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Abstract

Two enantiomeric pairs of iron(ii) metallohelices, available as water-soluble, stable, and optically pure bimetallic complexes, differ principally in the length of the central hydrophobic region between two cationic domains, and have distinct activity and cell selectivity profiles against Gram-positive and Gram-negative microbes. The effects of dose concentration and temperature on levels of intracellular accumulation in E. coli and S. aureus, studied via isotopic labelling, indicate that the metallohelices enter the microbial cells via passive diffusion, whereupon (as previously determined) they act on intracellular targets. Whilst the metallohelices with the shorter central hydrophobic regions accumulate less readily than those with the longer hydrophobic bridge in both E. coli and S. aureus cells when incubated at the same concentration, an order of magnitude less is actually required per cell to inhibit growth in E. coli, hence they are more active. Furthermore, these more Gram-negative active compounds (with the shorter central hydrophobic region) are less toxic towards human APRE-19 mammalian cells and equine red blood cells. We hypothesise that these cell selectivities originate from the membrane composition. Dynamic light scattering and zeta potential measurements demonstrate that the more lipophilic metallohelices interact more strongly with the membrane-mimetic vesicles, notably in the charge-neutral mammalian model; thus the selectivity is not simply a result of electrostatic effects. For the less lipophilic metallohelices we observe that the binding affinity with the E. coli model vesicles is greater than with S. aureus vesicles, despite the lower negative surface charge, and this corresponds with the cellular accumulation data and the measured MICs. Specifically, the presence of membrane phosphatidylethanolamine (POPE) significantly increases the binding affinity of these metallohelices, and we postulate that a high proportion of such conical, non-lamellar phospholipids is important for metallohelix transport across the membrane. The metallohelices with the shorter hydrophobic bridge studied have a balance of charge and lipophilicity which allows selective cell entry in E. coli over mammalian cells, while the more lipophilic metallohelices are membrane promiscuous and unselective.

膜脂组成指导抗菌金属螺旋的细胞选择性。
铁(ii)金属螺旋对映体是水溶性的、稳定的、光学纯的双金属配合物,它们在两个阳离子结构域之间的中心疏水区域的长度主要不同,并且对革兰氏阳性和革兰氏阴性微生物具有不同的活性和细胞选择性。通过同位素标记研究了剂量浓度和温度对大肠杆菌和金黄色葡萄球菌细胞内积聚水平的影响,表明金属螺旋通过被动扩散进入微生物细胞,然后(如先前确定的)它们作用于细胞内靶点。虽然在相同浓度下,具有较短中心疏水区域的金属螺旋比具有较长疏水桥的金属螺旋更不容易在大肠杆菌和金黄色葡萄球菌细胞中积累,但实际上每个细胞抑制大肠杆菌生长所需的金属螺旋要少一个数量级,因此它们更活跃。此外,这些革兰氏阴性活性化合物(具有较短的中心疏水区)对人类APRE-19哺乳动物细胞和马红细胞的毒性较小。我们假设这些细胞的选择性源于膜的组成。动态光散射和zeta电位测量表明,亲脂性越强的金属螺旋与模拟膜囊泡的相互作用越强,特别是在电荷中性的哺乳动物模型中;因此,选择性不仅仅是静电效应的结果。对于亲脂性较差的金属螺旋,我们观察到与大肠杆菌模型囊泡的结合亲和力大于与金黄色葡萄球菌囊泡的结合亲和力,尽管其表面负电荷较低,这与细胞积累数据和测量的mic相一致。具体来说,膜磷脂酰乙醇胺(POPE)的存在显著增加了这些金属螺旋的结合亲和力,我们假设这种圆锥形、非片层状磷脂的高比例对金属螺旋跨膜运输很重要。具有较短疏水桥的金属螺旋具有电荷平衡和亲脂性,可以选择性地进入大肠杆菌而不是哺乳动物细胞,而亲脂性较强的金属螺旋则具有膜混杂性和非选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
129
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