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ATR-FTIR 光谱法的应用及 DNA 构象的可逆性作为传感器检测铂(II)抗癌药物的效果。

The Application of ATR-FTIR Spectroscopy and the Reversible DNA Conformation as a Sensor to Test the Effectiveness of Platinum(II) Anticancer Drugs.

机构信息

Centre for Biospectroscopy and School of Chemistry, Monash University, Clayton, VIC 3800, Australia.

School of Chemistry, Monash University, Clayton, VIC 3800, Australia.

出版信息

Sensors (Basel). 2018 Dec 6;18(12):4297. doi: 10.3390/s18124297.

Abstract

Platinum(II) complexes have been found to be effective against cancer cells. Cisplatin curbs cell replication by interacting with the deoxyribonucleic acid (DNA), reducing cell proliferation and eventually leading to cell death. In order to investigate the ability of platinum complexes to affect cancer cells, two examples from the class of polyfluorophenylorganoamidoplatinum(II) complexes were synthesised and tested on isolated DNA. The two compounds -,'-bis(2,3,5,6-tetrafluorophenyl)ethane-1,2-diaminato(1-)(pyridine)platinum(II) (PFB) and -,'-bis(2,3,5,6-tetrafluorophenyl)ethane-1,2-diaminato(1-)(pyridine)platinum(II) (TMB) were compared with cisplatin through their reaction with DNA. Attenuated Total Reflection Fourier Transform Infrared (ATR-FTIR) spectroscopy was applied to analyse the interaction of the Pt complexes with DNA in the hydrated, dehydrated and rehydrated states. These were compared with control DNA in acetone/water (PFB, TMB) and isotonic saline (cisplatin) under the same conditions. Principle Component Analysis (PCA) was applied to compare the ATR-FTIR spectra of the untreated control DNA with spectra of PFB and TMB treated DNA samples. Disruptions in the conformation of DNA treated with the Pt complexes upon rehydration were mainly observed by monitoring the position of the IR-band around 1711 cm assigned to the DNA base-stacking vibration. Furthermore, other intensity changes in the phosphodiester bands of DNA at ~1234 cm and 1225 cm and shifts in the dianionic phosphodiester vibration at 966 cm were observed. The isolated double stranded DNA (dsDNA) or single stranded DNA (ssDNA) showed different structural changes when incubated with the studied compounds. PCA confirmed PFB had the most dramatic effect by denaturing both dsDNA and ssDNA. Both compounds, along with cisplatin, induced changes in DNA bands at 1711, 1088, 1051 and 966 cm indicative of DNA conformation changes. The ability to monitor conformational change with infrared spectroscopy paves the way for a sensor to screen for new anticancer therapeutic agents.

摘要

铂(II)配合物已被发现对癌细胞有效。顺铂通过与脱氧核糖核酸 (DNA) 相互作用来抑制细胞复制,从而降低细胞增殖,最终导致细胞死亡。为了研究铂配合物影响癌细胞的能力,我们合成了两类多氟苯基有机酰胺铂(II)配合物,并在分离的 DNA 上进行了测试。两种化合物 -,'-双(2,3,5,6-四氟苯基)乙烷-1,2-二胺基(1-)(吡啶)铂(II) (PFB) 和 -,'-双(2,3,5,6-四氟苯基)乙烷-1,2-二胺基(1-)(吡啶)铂(II) (TMB) 与顺铂进行了比较,研究了它们与 DNA 的反应。衰减全反射傅里叶变换红外 (ATR-FTIR) 光谱被用于分析 Pt 配合物与水合、脱水和再水合状态下 DNA 的相互作用。将这些与在相同条件下用丙酮/水 (PFB、TMB) 和等渗盐水 (顺铂) 处理的对照 DNA 进行了比较。主成分分析 (PCA) 被用于比较未经处理的对照 DNA 的 ATR-FTIR 光谱与 PFB 和 TMB 处理的 DNA 样本的光谱。通过监测分配给 DNA 碱基堆积振动的约 1711cm-1 的 IR 带的位置,主要观察到 DNA 与 Pt 配合物处理后重新水合时构象的破坏。此外,还观察到 DNA 的磷酸二酯带在~1234cm 和 1225cm 处的其他强度变化以及二价磷酸二酯振动在 966cm 处的位移。当与研究化合物孵育时,分离的双链 DNA (dsDNA) 或单链 DNA (ssDNA) 表现出不同的结构变化。PCA 证实 PFB 通过使 dsDNA 和 ssDNA 变性而产生最显著的影响。两种化合物以及顺铂都诱导了 1711、1088、1051 和 966cm 处 DNA 带的变化,表明 DNA 构象发生了变化。用红外光谱监测构象变化的能力为筛选新的抗癌治疗剂铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e546/6308638/4ecfa8823a4f/sensors-18-04297-g001.jpg

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