Central Laser Facility, Science & Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Campus, Didcot, Oxfordshire OX11 0QX, UK; Larch House, Woodlands Business Park, Breckland, Linford Wood, Milton Keynes MK14 6FG, UK.
Central Laser Facility, Science & Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Campus, Didcot, Oxfordshire OX11 0QX, UK.
J Photochem Photobiol B. 2020 Dec;213:112055. doi: 10.1016/j.jphotobiol.2020.112055. Epub 2020 Oct 15.
The range of cellular functions the mechanistic target of rapamycin (mTOR) protein performs makes it an attractive drug target for cancer therapy. However, the cellular localisation and mode of action of second generation inhibitors of mTOR is poorly understood despite the level of attention there is in targeting the mTOR protein. We have therefore studied the properties of the pan-mTOR inhibitor AZD2014, an ideal candidate to study because it is naturally fluorescent, characterising its photochemical properties in solution phase (DMSO, PBS and BSA) and within living cells, where it localises within both the nucleus and the cytoplasm but with different excited state lifetimes of 4.8 (+/- 0.5) and 3.9 (+/- 0.4) ns respectively. We measure the uptake of the inhibitor AZD2014 (7 μM) in monolayer HEK293 cells occurring with a half-life of 1 min but observe complex behaviour for 3D spheroids with the core of the spheroid showing a slower uptake and a slow biphasic behaviour at longer times. From a cellular perspective using fluorescence lifetime imaging microscopy AZD2014 was found to interact directly with GFP-tagged mTORC1 proteins including the downstream target, S6K1. We observe light sensitive behaviour of the cells containing AZD2014 which leads to cell death, in both monolayer and spheroids cells, demonstrating the potential of AZD2014 to act as a possible photodynamic drug under both single photon and multiphoton excitation and discuss its use as a photosensitizer. We also briefly characterise another pan-mTOR inhibitor, INK128.
雷帕霉素的作用靶点(mTOR)蛋白所执行的细胞功能范围使其成为癌症治疗的有吸引力的药物靶标。然而,尽管 mTOR 蛋白是靶向治疗的热点,但第二代 mTOR 抑制剂的细胞定位和作用模式仍了解甚少。因此,我们研究了 pan-mTOR 抑制剂 AZD2014 的特性,它是研究的理想候选物,因为它具有天然荧光性,我们在溶液相(DMSO、PBS 和 BSA)和活细胞中对其光化学性质进行了表征,在活细胞中,它定位于细胞核和细胞质内,但激发态寿命分别为 4.8(+/-0.5)和 3.9(+/-0.4)ns。我们测量了单层 HEK293 细胞中抑制剂 AZD2014(7μM)的摄取,半衰期为 1 分钟,但观察到 3D 球体的复杂行为,球体的核心显示出较慢的摄取和较慢的双相行为较长时间。从细胞角度来看,使用荧光寿命成像显微镜发现 AZD2014 直接与 GFP 标记的 mTORC1 蛋白相互作用,包括下游靶标 S6K1。我们观察到含有 AZD2014 的细胞表现出光敏感行为,导致细胞死亡,无论是在单层细胞还是球体细胞中,这表明 AZD2014 在单光子和多光子激发下都有可能作为一种光动力药物,并讨论了其作为光敏剂的应用。我们还简要描述了另一种 pan-mTOR 抑制剂 INK128。