Bates P J, Dosanjh H S, Kumar S, Jenkins T C, Laughton C A, Neidle S
CRC Biomolecular Structure Unit, Institute of Cancer Research, Sutton, Surrey, UK.
Nucleic Acids Res. 1995 Sep 25;23(18):3627-32. doi: 10.1093/nar/23.18.3627.
Real-time biomolecular interaction analysis (BIA) has been applied to triplex formation between oligodeoxynucleotides. 5'-Biotinylated oligonucleotides were immobilised on the streptavidin-coated surface of a biosensor chip and subsequently hybridised to their complementary strand. Sequence-specific triplex formation was observed when a suitable third-strand oligopyrimidine was injected over the surface-bound duplex. In addition, a single-stranded oligonucleotide immobilised on the chip surface was able to capture a DNA duplex by triplex recognition. The presence of spermine increases the rate of association between the third strand and immobilised duplex, but at elevated spermine concentrations non-specific association is observed. A preliminary kinetic analysis of triplex formation at pH 5.2 by an 11mer third strand containing thymine, cytosine and uracil is reported. Values for the association and dissociation rate constants were determined to be (1.9 +/- 0.2) x 10(3) M-1 s-1 and (8.1 +/- 1.9) x 10(-5) s-1, respectively.
实时生物分子相互作用分析(BIA)已应用于寡脱氧核苷酸之间三链体的形成。5'-生物素化的寡核苷酸固定在生物传感器芯片的链霉亲和素包被表面,随后与它们的互补链杂交。当在表面结合的双链体上注入合适的第三链寡嘧啶时,观察到序列特异性三链体的形成。此外,固定在芯片表面的单链寡核苷酸能够通过三链体识别捕获DNA双链体。精胺的存在增加了第三链与固定双链体之间的结合速率,但在精胺浓度升高时会观察到非特异性结合。报道了由含胸腺嘧啶、胞嘧啶和尿嘧啶的11聚体第三链在pH 5.2时三链体形成的初步动力学分析。结合和解离速率常数的值分别确定为(1.9±0.2)×10³ M⁻¹ s⁻¹和(8.1±1.9)×10⁻⁵ s⁻¹。