Kobori Akio, Nakatani Kazuhiko
Department of Biomolecular Engineering, Graduate School of Science and Technology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
Bioorg Med Chem. 2008 Dec 15;16(24):10338-44. doi: 10.1016/j.bmc.2008.10.035. Epub 2008 Oct 17.
Discrimination of base mismatches from normal Watson-Crick base pairs in duplex DNA constitutes a key approach to the detection of single nucleotide polymorphisms (SNPs). We have developed a sensor for a surface plasmon resonance (SPR) assay system to detect G-G, A-A, and C-C mismatch duplexes by employing a surface upon which mismatch-binding ligands (MBLs) are immobilized. We synthesized a new MBL consisting of 2,7-diamino-1,8-naphthyridine (damND) and immobilized it onto a CM5 sensor chip to carry out the SPR assay of DNA duplexes containing a single-base mismatch. The SPR sensor with damND revealed strong responses to all C-C mismatches, and sequence-dependent C-T and T-T mismatches. Compared to ND- and naphthyridine-azaquinolone hybrid (NA)-immobilized sensor surfaces, with affinity to mismatches composed of purine nucleotide bases, the damND-immobilized surface was useful for the detection of the mismatches composed of pyrimidine nucleotide bases.
区分双链DNA中正常的沃森-克里克碱基对与碱基错配是检测单核苷酸多态性(SNP)的关键方法。我们开发了一种用于表面等离子体共振(SPR)检测系统的传感器,通过使用固定有错配结合配体(MBL)的表面来检测G-G、A-A和C-C错配双链体。我们合成了一种由2,7-二氨基-1,8-萘啶(damND)组成的新型MBL,并将其固定在CM5传感器芯片上,以对含有单碱基错配的DNA双链体进行SPR检测。带有damND的SPR传感器对所有C-C错配以及序列依赖性的C-T和T-T错配都有强烈响应。与固定有对由嘌呤核苷酸碱基组成的错配具有亲和力的ND和萘啶-氮杂喹诺酮杂交体(NA)的传感器表面相比,固定有damND的表面可用于检测由嘧啶核苷酸碱基组成的错配。