†AG Biophysik, I. Physikalisches Institut (IA), RWTH Aachen University, 52062 Aachen, Germany.
‡Molecular Biophysics, Institute of Complex Systems (ICS-5), Forschungszentrum Jülich, 52428 Jülich, Germany.
J Phys Chem B. 2015 Apr 2;119(13):4668-72. doi: 10.1021/acs.jpcb.5b02170. Epub 2015 Mar 24.
Here, we present a comparative method for the accurate determination of fluorescence quantum yields (QYs) by fluorescence correlation spectroscopy. By exploiting the high sensitivity of single-molecule spectroscopy, we obtain the QYs of samples in the microliter range and at (sub)nanomolar concentrations. Additionally, in combination with fluorescence lifetime measurements, our method allows the quantification of both static and collisional quenching constants. Thus, besides being simple and fast, our method opens up the possibility to photophysically characterize labeled biomolecules under application-relevant conditions and with low sample consumption, which is often important in single-molecule studies.
在这里,我们提出了一种通过荧光相关光谱法准确测定荧光量子产率(QYs)的比较方法。通过利用单分子光谱的高灵敏度,我们可以在微升范围内和(亚)纳摩尔浓度下获得样品的 QY 值。此外,通过与荧光寿命测量相结合,我们的方法可以定量测定静态和碰撞猝灭常数。因此,除了简单快速之外,我们的方法还为在相关应用条件下用光物理特性表征标记生物分子提供了可能性,并且样品消耗量低,这在单分子研究中通常很重要。