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Peptide-Bridged Dinuclear Ru(Ⅱ) Complex for Mitochondrial Targeted Monitoring of Dynamic Changes to Oxygen Concentration and ROS Generation in Live Mammalian Cells

机译:肽桥联双核Ru(Ⅱ)络合物用于线粒体靶向监测活哺乳动物细胞中氧浓度和ROS生成的动态变化

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摘要

A novel mitochondrial localizing ruthenium(Ⅱ) peptide conjugate capable of monitoring dynamic changes in local O_2 concentrations within living cells is presented. The complex is comprised of luminescent dinuclear ruthenium(Ⅱ) polypyridyl complex bridged across a single mitochondrial penetrating peptide, FrFKFrFK-CONH_2 (r = D-arginine). The membrane permeability and selective uptake of the peptide conjugate at the mitochondria of mammalian cells was demonstrated using confocal microscopy. Dye co-localization studies confirmed very precise localization and preconcentration of the probe at the mitochondria. This precision permitted collection of luminescent lifetime images of the probe, without the need for co-localizing dye and permitted semiquantitative determination of oxygen concentration at the mitochondria using calibration curves collected at 37 ℃ for the peptide conjugate in PBS buffer. Using Antimycin A the ability of the probe to respond dynamically to changing O_2 concentrations within live HeLa cells was demonstrated. Furthermore, based on lifetime data it was evident that the probe also responds to elevated reactive oxygen species (ROS) levels within the mitochondria, where the greater quenching capacity of these species led to luminescent lifetimes of the probe at longer Antimycin A incubation times which lay outside of the O_2 concentration range. Although both the dinuclear complex and a mononudear analogue conjugated to an octaarginine peptide sequence exhibited some cytotoxicity over 24 h, cells were tolerant of the probes over periods of 4 to 6 h which facilitated imaging. These metal-peptide conjugated probes offer a valuable opportunity for following dynamic changes to mitochondrial function which should be of use across domains in which the metabolic activity of live cells are of interest from molecular biology and drug discovery.
机译:提出了一种能够监测活细胞内局部O_2浓度动态变化的线粒体定位钌(Ⅱ)肽共轭物。该复合物由跨单个线粒体穿透肽FrFKFrFK-CONH_2(r = D-精氨酸)桥接的发光双核钌(Ⅱ)聚吡啶基复合物组成。使用共聚焦显微镜证实了膜结合物在哺乳动物细胞线粒体的膜通透性和选择性摄取。染料共定位研究证实,探针在线粒体上的定位和浓度非常精确。该精度允许收集探针的发光寿命图像,而无需共定位染料,并且可以使用在37℃下收集的PBS缓冲液中肽结合物的校准曲线半定量测定线粒体中的氧浓度。使用抗霉素A,证明了探针对活的HeLa细胞内O_2浓度变化具有动态响应的能力。此外,根据寿命数据,很明显该探针还对线粒体内升高的活性氧(ROS)水平作出反应,其中这些物质的更大淬灭能力导致在更长的抗霉素A孵育时间下探针的发光寿命不在O_2浓度范围内。尽管双核复合物和与八精氨酸肽序列缀合的单核类似物在24小时内均表现出一定的细胞毒性,但细胞在4至6小时内对探针耐受,这有利于成像。这些金属肽偶联的探针为线粒体功能的动态变化提供了宝贵的机会,线粒体功能的动态变化应在跨域使用,分子生物学和药物发现对活细胞的代谢活性感兴趣。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2014年第43期|15300-15309|共10页
  • 作者单位

    School of Chemical Sciences, National Biophotonics and Imaging Platform, Dublin City University, Dublin 9, Ireland;

    School of Chemical Sciences, National Biophotonics and Imaging Platform, Dublin City University, Dublin 9, Ireland;

    School of Chemical Sciences, National Biophotonics and Imaging Platform, Dublin City University, Dublin 9, Ireland;

    School of Chemical Sciences, National Biophotonics and Imaging Platform, Dublin City University, Dublin 9, Ireland;

    School of Chemical Sciences, National Biophotonics and Imaging Platform, Dublin City University, Dublin 9, Ireland;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:11:14

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