Rogers Y H, Jiang-Baucom P, Huang Z J, Bogdanov V, Anderson S, Boyce-Jacino M T
Alpha Center, Johns Hopkins Bayview Research Campus, 5210 Eastern Avenue, Baltimore, Maryland, 21224, USA.
Anal Biochem. 1999 Jan 1;266(1):23-30. doi: 10.1006/abio.1998.2857.
The covalent attachment of disulfide-modified oligonucleotides to a mercaptosilane-modified glass surface is described. This method provides an efficient and specific covalent attachment chemistry for immobilization of DNA probes onto a solid support. Glass slides were derivatized with 3-mercaptopropyl silane for attachment of 5-prime disulfide-modified oligonucleotides via disulfide bonds. An attachment density of approximately 3 x 10(5) oligonucleotides/microm2 was observed. Oligonucleotides attached by this method provided a highly efficient substrate for nucleic acid hybridization and primer extension assays. In addition, we have demonstrated patterning of multiple DNA probes on a glass surface utilizing this attachment chemistry, which allows for array densities of at least 20,000 spots/cm2.
本文描述了二硫键修饰的寡核苷酸与巯基硅烷修饰的玻璃表面的共价连接。该方法为将DNA探针固定到固体支持物上提供了一种高效且特异的共价连接化学方法。用3-巯基丙基硅烷对玻片进行衍生化,以便通过二硫键连接5'-二硫键修饰的寡核苷酸。观察到的连接密度约为3×10⁵个寡核苷酸/μm²。通过这种方法连接的寡核苷酸为核酸杂交和引物延伸分析提供了高效的底物。此外,我们已经证明利用这种连接化学方法可以在玻璃表面对多个DNA探针进行图案化,这使得阵列密度至少达到20,000个点/cm²。