Researcher, Laboratory of New Medical Materials and Technologies, Professional Center for Education and Research in Genetic and Laboratory Technologies; Assistant, Chemistry Department, Pharmacy Institute; Samara State Medical University, 89 Chapaevskaya St., Samara, 443099, Russia.
Leading Researcher, Laboratory of Non-Infectious Immunology, Professional Center for Education and Research in Genetic and Laboratory Technologies; Samara State Medical University, 89 Chapaevskaya St., Samara, 443099, Russia.
Sovrem Tekhnologii Med. 2024;16(1):5-13. doi: 10.17691/stm2024.16.1.01. Epub 2024 Feb 28.
was to assess the capabilities of human genomic DNA biomineralization into ZIF-8 metal-organic framework (MOF) preserving DNA sequence integrity after the encapsulation cycle and composite dissolving. The study is an initial stage of the project aimed at developing an abiotic vector to be used when working with native nucleic acids of an arbitrary size based on DNA@ZIF-8 composite.
We studied human genomic DNA isolated from lymphocytes of peripheral blood of healthy volunteers using Proba-NK kit (DNA-Technology LLC, Russia). Genomic DNA purity and concentration was estimated spectrophotometrically at 260/280 nm using Tecan Infinity 200 Pro plate reader (Tecan Instruments, Austria). ZIF-8 was synthesized in the physiological conditions (37°C) by mixing zinc salt and 2-methylimidazole aqueous solutions at different molar ratios. Human genomic DNA was encapsulated into ZIF-8 in similar conditions. The obtained MOF and DNA@ZIF-8 composite were studied using X-ray powder diffraction at the Phaser D2 XRPD device (Bruker, USA), and the specific surface area was estimated using Autosorb iQ porosimetry analyzer (Quantachrome, USA). The encapsulated DNA was quantified by dissolving DNA@ZIF-8 composite in the citrate buffer. DNA integrity was assessed by real-time allele-specific PCR (AS-PCR) using the kits for single nucleotide polymorphisms (Lytech, Russia) at the Quantstudio 6 Pro PCR machine (Thermo Scientific, USA). In case of using the kits with electrophoretic detection, the amplification was performed on the thermal cycler T100 (Thermo Scientific, USA).
The polymer ZIF-8 and DNA@ZIF-8 composite were obtained at different molar ratios of zinc ions and 2-methylimidazole. We characterized their structure and specific surface area. Genomic DNA biomineralization efficacy was found to be about 7-8%. PCR indicated the integrity of non-selectively chosen loci within the biomineralized DNA.
The study confirmed the possibility of human genomic DNA encapsulation into ZIF-8 metal-organic framework. After the biomineralization, DNA was found to preserve feasibility to be used in studies to investigate genetic constructs.
评估人类基因组 DNA 生物矿化到 ZIF-8 金属有机骨架(MOF)中的能力,以在封装循环和复合材料溶解后保持 DNA 序列完整性。该研究是一个项目的初始阶段,旨在开发一种非生物载体,用于处理任意大小的天然核酸,基于 DNA@ZIF-8 复合材料。
我们使用 Proba-NK 试剂盒(DNA-Technology LLC,俄罗斯)从健康志愿者外周血淋巴细胞中分离出人基因组 DNA。使用 Tecan Infinity 200 Pro 板读数器(Tecan Instruments,奥地利)在 260/280nm 处分光光度法估计基因组 DNA 的纯度和浓度。在生理条件(37°C)下,通过混合锌盐和 2-甲基咪唑水溶液以不同的摩尔比合成 ZIF-8。在类似条件下将人基因组 DNA 封装到 ZIF-8 中。使用 X 射线粉末衍射在 Phaser D2 XRPD 设备(Bruker,美国)上研究获得的 MOF 和 DNA@ZIF-8 复合材料,并使用 Autosorb iQ 孔隙率分析仪(Quantachrome,美国)估计比表面积。通过在柠檬酸缓冲液中溶解 DNA@ZIF-8 复合材料来定量测定封装的 DNA。通过使用 Lytech,俄罗斯)试剂盒在 Quantstudio 6 Pro PCR 仪(Thermo Scientific,美国)上进行实时等位基因特异性 PCR(AS-PCR)评估 DNA 完整性。在使用具有电泳检测试剂盒的情况下,在 T100 热循环仪(Thermo Scientific,美国)上进行扩增。
在不同摩尔比的锌离子和 2-甲基咪唑下获得了聚合物 ZIF-8 和 DNA@ZIF-8 复合材料。我们对其结构和比表面积进行了表征。发现基因组 DNA 生物矿化效率约为 7-8%。PCR 表明非选择性选择的生物矿化 DNA 内基因座的完整性。
该研究证实了将人基因组 DNA 封装到 ZIF-8 金属有机骨架中的可能性。在生物矿化后,发现 DNA 具有可用于研究遗传结构的可行性。