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聚合物涂层载玻片作为光学寡核苷酸微阵列的开发。

Development of polymer-coated glass slides as optical oligonucleotide microarrays.

作者信息

Pourjahed Atefeh, Rabiee Mohammad, Tahriri Mohammadreza

机构信息

Biomaterials Group, Faculty of Biomedical Engineering, Amirkabir University of Technology, Tehran, Iran.

出版信息

Avicenna J Med Biotechnol. 2013 Oct;5(4):241-50.

Abstract

BACKGROUND

The microarray technology is in needed of cost-effective, low background noise and stable substrates for successful hybridization and analysis.

METHODS

In this research, we developed a three-dimentional stable and mechanically reliable microarray substrates by coating of two polymeric layers on standard microscope glass slides. For fabrication of these substrates, a thin film of oxidized agarose was prepared on the Poly-L-Lysine (PLL) coated glass slides. Unmodified oligonucleotide probes were spotted and immobilized on these double layered thin films by adsorption on the porous structure of the agarose film. Some of the aldehyde groups of the activated agarose linked covalently to PLL amine groups; on the other side, they bound to amino groups of adsorbed tail of biomolecules. These linkages were fixed by UV irradiation at 254 nm using a CL-1000 UV. These prepared substrates were compared to only agarose-coated and PLL-coated slides.

RESULTS

Atomic Force Microscope (AFM) results demonstrated that agarose provided three-dimensional surface which had higher loading and bindig capacity for biomolecules than PLL-coated surface which had two-dimensional surface. The nano-indentation tests demonstrated the prepared double coating was more reliable and flexible for mechanical robotic spotting. In addition, the repeated indentation on different substrates showed uniformity of coatings. The stability of novel coating was sufficient for hybridization process. The signal-to-noise ratio in hybridization reactions performed on the agarose-PLL coated substrates increased two fold and four fold compared to agarose and PLL coated substrates, respectively.

CONCLUSION

Finally, the agarose-PLL microarrays had the highest signal (2920) and lowest background signal (205) in hybridization, suggesting that the prepared slides are suitable in analyzing wide concentration range of analytes.

摘要

背景

微阵列技术需要具有成本效益、低背景噪音且稳定的基质,以实现成功的杂交和分析。

方法

在本研究中,我们通过在标准显微镜载玻片上涂覆两层聚合物层,开发出一种三维稳定且机械性能可靠的微阵列基质。为制备这些基质,在聚-L-赖氨酸(PLL)包被的载玻片上制备一层氧化琼脂糖薄膜。将未修饰的寡核苷酸探针点样并通过吸附在琼脂糖薄膜的多孔结构上固定在这些双层薄膜上。活化琼脂糖的一些醛基与PLL胺基共价连接;另一方面,它们与生物分子吸附尾的氨基结合。使用CL-1000紫外线在254nm下通过紫外线照射固定这些连接。将这些制备的基质与仅涂有琼脂糖和PLL的载玻片进行比较。

结果

原子力显微镜(AFM)结果表明,琼脂糖提供了三维表面,其对生物分子的负载和结合能力高于具有二维表面的PLL包被表面。纳米压痕测试表明,制备的双层涂层对于机械自动点样更可靠且更具柔韧性。此外,在不同基质上的重复压痕显示涂层具有均匀性。新型涂层的稳定性足以满足杂交过程。与琼脂糖和PLL包被的基质相比,在琼脂糖-PLL包被的基质上进行的杂交反应中的信噪比分别提高了两倍和四倍。

结论

最后,琼脂糖-PLL微阵列在杂交中具有最高信号(2920)和最低背景信号(205),表明制备的载玻片适用于分析宽浓度范围的分析物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/496d/3838769/3d48edb1d01c/AJMB-5-241-g001.jpg

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