National Institute of Standards and Technology, 100 Bureau Drive, Gaithersburg, MD 20899, USA.
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2010 Jan-Feb;2(1):48-58. doi: 10.1002/wnan.62.
We present results on the dynamic fluorescence properties of bioconjugated nanocrystals or quantum dots (QDs) in different chemical and physical environments. A variety of QD samples was prepared and compared: isolated individual QDs, QD aggregates, and QDs conjugated to other nanoscale materials, such as single-wall carbon nanotubes (SWCNTs) and human erythrocyte plasma membrane proteins. We discuss plausible scenarios to explain the results obtained for the fluorescence characteristics of QDs in these samples, especially for the excitation time-dependent fluorescence emission from clustered QDs. We also qualitatively demonstrate enhanced fluorescence emission signals from clustered QDs and deduce that the band 3 membrane proteins in erythrocytes are clustered. This approach is promising for the development of QD-based quantitative molecular imaging techniques for biomedical studies involving biomolecule clustering.
我们展示了在不同化学和物理环境中生物共轭纳米晶体或量子点(QD)的动态荧光性质的结果。制备和比较了各种 QD 样品:孤立的单个 QD、QD 聚集体以及与其他纳米材料(如单壁碳纳米管(SWCNT)和人红细胞质膜蛋白)共轭的 QD。我们讨论了可能的情况来解释这些样品中 QD 荧光特性的结果,特别是对于聚集 QD 的激发时间依赖性荧光发射。我们还定性地证明了聚集 QD 的荧光发射信号增强,并推断红细胞中的带 3 膜蛋白是聚集的。这种方法有望为涉及生物分子聚集的生物医学研究开发基于 QD 的定量分子成像技术。