Wolf Lauren K, Fullenkamp Dominic E, Georgiadis Rosina M
Department of Chemistry, Boston University, 590 Commonwealth Avenue, Boston, Massachusetts 02215, USA.
J Am Chem Soc. 2005 Dec 14;127(49):17453-9. doi: 10.1021/ja056422w.
We demonstrate the quantitative characterization of DNA-DNA and DNA-drug interactions by angle-resolved surface plasmon resonance (SPR) imaging. Combining the angle-scanning capabilities of traditional SPR with the spatial definition capabilities of imaging, we directly measure DNA and drug surface coverages and kinetics simultaneously for multiple patterned spots. We find excellent agreement of DNA-DNA hybridization kinetics and thermodynamics measured by both the imaging system and traditional SPR. Instrument response and sensitivity is further demonstrated by successful measurement of association and dissociation kinetics of actinomycin-D binding to a low-density doubled-stranded DNA binding sequence. Without independent calibration, analysis of angle-resolved SPR imaging data yields 2.9 +/- 0.1 drugs per duplex at saturation coverage, consistent with all available duplex binding sites being occupied.
我们通过角分辨表面等离子体共振(SPR)成像展示了DNA-DNA和DNA-药物相互作用的定量表征。将传统SPR的角度扫描能力与成像的空间定义能力相结合,我们可以同时直接测量多个图案化斑点的DNA和药物表面覆盖率及动力学。我们发现成像系统和传统SPR测量的DNA-DNA杂交动力学和热力学结果高度一致。通过成功测量放线菌素-D与低密度双链DNA结合序列的结合和解离动力学,进一步证明了仪器的响应和灵敏度。在无需独立校准的情况下,对角分辨SPR成像数据的分析表明,在饱和覆盖率下,每个双链体有2.9±0.1个药物,这与所有可用的双链体结合位点都被占据的情况一致。