Institute for Bioscience & Biotechnology Research, University of Maryland, Rockville, MD 20850, USA.
Leicester School of Allied Health Sciences, Faculty of Health & Life Sciences, De Montfort University, The Gateway, Leicester, LE1 9BH, UK.
Nanomedicine (Lond). 2022 Nov;17(26):2011-2021. doi: 10.2217/nnm-2022-0204. Epub 2023 Feb 28.
To quantitatively evaluate the inhibition of human DNA repair proteins APE1 and MTH1 by dextran-coated γ-FeO ultrasmall superparamagnetic iron oxide nanoparticles (dUSPIONs). : Liquid chromatography-tandem mass spectrometry with isotope-dilution was used to measure the expression levels of APE1 and MTH1 in MCL-5 cells exposed to increasing doses of dUSPIONs. The expression levels of APE1 and MTH1 were measured in cytoplasmic and nuclear fractions of cell extracts. APE1 and MTH1 expression was significantly inhibited in both cell fractions at the highest dUSPION dose. The expression of MTH1 was linearly inhibited across the full dUSPION dose range in both fractions. These findings warrant further studies to characterize the capacity of dUSPIONs to inhibit other DNA repair proteins and .
为了定量评估葡聚糖包覆的γ-FeO 超顺磁性氧化铁纳米颗粒(dUSPIONs)对人 DNA 修复蛋白 APE1 和 MTH1 的抑制作用。采用液相色谱-串联质谱法(LC-MS/MS)和同位素稀释法,测量了暴露于递增剂量 dUSPIONs 的 MCL-5 细胞中 APE1 和 MTH1 的表达水平。测量了细胞提取物的细胞质和核部分中的 APE1 和 MTH1 的表达水平。在最高 dUSPION 剂量下,两种细胞部分的 APE1 和 MTH1 表达均显著受到抑制。两种部分的 MTH1 表达均在线性范围内受到 dUSPION 剂量全范围的抑制。这些发现需要进一步研究以表征 dUSPIONs 抑制其他 DNA 修复蛋白的能力。