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Plasmon-Resonance-Energy-Transfer-Based Spectroscopy on Single Nanoparticles: Biomolecular Recognition and Enzyme Kinetics

机译:单纳米颗粒上的等离子体共振 - 能量转移基光谱:生物分子识别和酶动力学

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摘要

The small absorption cross sections of most molecules led to the low sensitivity of traditional optical absorption spectroscopy. This obstacle might be overcome by applying the near-field plasmon resonance energy transfer (PRET) between plasmonic nanoparticle and surrounding molecules. In this work, we utilized PRET-based spectroscopy on single gold nanostars to study the specific biomolecule recognition and enzyme kinetics choosing biotin-SA pair and DNase I as models. By analyzing the changes of absorption spectra for black hole quencher 3 (BHQ3), derived from spectra difference, we explored the kinetics of specific biomolecule recognition and enzyme digestion in different physiological environment, and we found that the viscosities of media and the sizes of molecules play vital role in biomolecular recognition and enzyme digestion. Compared with the traditional optical absorption spectroscopy techniques, PRET-based spectroscopy offers a nanoscopic resolution owing to the small size of the probe, is more sensitive and achieves detection on the order of hundreds or even dozens of molecules, and can achieve high selectivity due to the specific biomolecular recognition. This method might be used in the fields of molecular diagnostics, drug discovery, cell systems, and clinical diagnostics.
机译:大多数分子的小吸收横截面导致了传统光学吸收光谱的低灵敏度。通过在等离子体纳米粒子和周围分子之间应用近场等离子体共振能量转移(PRIP),可能会克服该障碍。在这项工作中,我们在单金纳盘上使用了基于Pret-Count的光谱,研究了特定的生物分子识别和酶动力学选择生物素-SA对和DNase I作为模型。通过分析来自光谱差异的黑洞猝灭剂3(BHQ3)的吸收光谱的变化,我们探讨了不同生理环境中特定的生物分子识别和酶消化的动力学,并发现培养基的粘度和分子的尺寸在生物分子识别和酶消化中发挥至关重要的作用。与传统的光学吸收光谱技术相比,由于探头的尺寸小,预谱提供了纳米镜分辨率,更敏感,并达到数百甚至数十分子的检测,并且可以实现高选择性具体的生物分子识别。该方法可用于分子诊断,药物发现,细胞系统和临床诊断领域。

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