首页> 外文期刊>Journal of the American Chemical Society >Preorganized Bis-Thioureas as Powerful Anion Carriers: Chloride Transport by Single Molecules in Large Unilamellar Vesicles
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Preorganized Bis-Thioureas as Powerful Anion Carriers: Chloride Transport by Single Molecules in Large Unilamellar Vesicles

机译:作为有力的阴离子载体的预先组织的双硫脲:大型单层囊泡中单分子的氯化物运输。

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摘要

Transmembrane anion carriers (anionophores) have potential in biological research and medicine, provided high activities can be obtained. There is particular interest in treating cystic fibrosis (CF), a genetic illness caused by deficient anion transport. Previous work has found that anionophore designs featuring axial ureas on steroid and trans-decalin scaffolds can be especially effective. Here we show that replacement of ureas by thioureas yields substantial further enhancements. Six new bis-thioureas have been prepared and tested for Cl~-/NO_3~- exchange in 1-palmitoyl- 2-oleoylphosphatidylcholine/cholesterol large unilamellar vesicles (LUVs). The bis-thioureas are typically >10 times more effective than the corresponding ureas and are sufficiently active that transport by molecules acting singly in LUVs is readily detected. The highest activity is shown by decalin 9, which features N-(3,5-bis(trifluoromethyl)phenyl)thioureido and octyl ester substituents. A single molecule of transporter 9 in a 200 nm vesicle promotes Cl~-/NO_3~- exchange with a half-life of 45 s and an absolute rate of 850 chloride anions per second. Weight- for-weight, this carrier is only slightly less effective than CFTR, the natural anion channel associated with CF.
机译:跨膜阴离子载体(阴离子载体)在生物学研究和医学上具有潜力,只要能够获得高活性即可。特别需要治疗的是囊性纤维化(CF),这是由阴离子运输不足引起的遗传疾病。先前的工作发现,在类固醇和反式十氢化萘支架上采用轴向尿素的阴离子载体设计特别有效。在这里,我们表明用硫脲替代尿素可产生实质性的进一步提高。制备了六种新的双硫脲,并测试了其在1-棕榈酰基-2-油酰基磷脂酰胆碱/胆固醇大的单层囊泡(LUV)中的Cl- / NO_3-交换。双硫脲的效力通常是相应脲的> 10倍,并且具有足够的活性,可以很容易地检测到在LUV中单独起作用的分子的转运。十氢化萘9表现出最高的活性,十氢化萘9具有N-(3,5-双(三氟甲基)苯基)硫脲基和辛基酯取代基。 200 nm囊泡中的单个转运蛋白9分子促进Cl _- / NO_3-交换,半衰期为45 s,绝对速率为每秒850个氯阴离子。以重量计,这种载体的功效仅略低于CFTR(CF的天然阴离子通道)的功效。

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  • 来源
    《Journal of the American Chemical Society》 |2014年第35期|12507-12512|共6页
  • 作者单位

    School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 4LN, United Kingdom;

    School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 4LN, United Kingdom;

    School of Physiology and Pharmacology, University of Bristol, University Walk, Bristol BS8 1TD, United Kingdom;

    School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 4LN, United Kingdom;

    School of Physiology and Pharmacology, University of Bristol, University Walk, Bristol BS8 1TD, United Kingdom;

    School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 4LN, United Kingdom;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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