Shliapnikova E A, Shliapnikov Iu M, Afanas'ev V N, Afanas'eva G V, Gavriushkin A V, Beletskiĭ I P
Bioorg Khim. 2007 Mar-Apr;33(2):261-8.
A set of methods for analysis of the quality of aminated substrates that could be a basis for the large-scale manufacturing of biological microchips is suggested. The analysis includes the determination of the number of amino groups, their availability for the immobilization of phosphorylated oligonucleotides, and the characterization of surface properties of the substrates in respect to the nonspecific sorption of reagents during hybridization. A simple procedure was suggested for determination of the density/number of amino groups. It is based on the use of dimethoxytrityl chloride with the subsequent spectrophotometric determination of dimethoxytrityl cation. The availability of amino groups was estimated by covalent attachment of an oligonucleotide probe containing a fluorescently labeled group to the aminated surface and the subsequent comparison of the intensity of fluorescing zones formed on the chip. The sorption properties of the surface were investigated with the help of a model hybridization reaction. A comparative analysis of aminated glasses manufactured by various firms and in our laboratory showed that the glasses with the amino group density from 0.7 to 2.0 groups/nm2 prepared by our procedure have the best properties for the hybridization analysis.
提出了一套用于分析胺化底物质量的方法,这些方法可作为生物微芯片大规模制造的基础。该分析包括氨基数量的测定、其用于固定磷酸化寡核苷酸的可用性,以及在杂交过程中底物表面性质对于试剂非特异性吸附的表征。提出了一种简单的测定氨基密度/数量的程序。它基于使用氯代二甲氧基三苯甲基,随后通过分光光度法测定二甲氧基三苯甲基阳离子。通过将含有荧光标记基团的寡核苷酸探针共价连接到胺化表面,并随后比较芯片上形成的荧光区强度来估计氨基的可用性。借助模型杂交反应研究了表面的吸附特性。对不同公司以及我们实验室制造的胺化玻璃进行的比较分析表明,通过我们的程序制备的氨基密度为0.7至2.0个基团/nm²的玻璃对于杂交分析具有最佳性能。