Rabasovic M D, Sisamakis E, Wennmalm S, Widengren J
Dept. Exp. Biomolecular Physics/Applied Physics, Royal Institute of Technology-KTH, Albanova University Center, 10691, Stockholm, Sweden.
Institute of Physics, University of Belgrade, Pregrevica 118, 11080, Belgrade-Zemun, Serbia.
Chemphyschem. 2016 Apr 4;17(7):1025-33. doi: 10.1002/cphc.201501129. Epub 2016 Feb 11.
Nanoparticles (NPs) and molecules can be analyzed by inverse fluorescence correlation spectroscopy (iFCS) as they pass through an open detection volume, displacing fractions of the fluorescence-emitting solution in which they are dissolved. iFCS does not require the NPs or molecules to be labeled. However, fluorophores in μm-mm concentrations are needed for the solution signal. Here, we instead use coherent anti-Stokes Raman scattering (CARS) from plain water molecules as the signal from the solution. By this fully label-free approach, termed inverse CARS-based correlation spectroscopy (iCARS-CS), NPs that are a few tenths of nm in diameter and at pM concentrations can be analyzed, and their absolute volumes/concentrations can be determined. Likewise, lipid vesicles can be analyzed as they diffuse/flow through the detection volume by using CARS fluctuations from the surrounding water molecules. iCARS-CS could likely offer a broadly applicable, label-free characterization technique of, for example, NPs, small lipid exosomes, or microparticles in biomolecular diagnostics and screening, and can also utilize CARS signals from biologically relevant media other than water.
纳米颗粒(NPs)和分子在通过开放检测体积时,会取代它们所溶解的荧光发射溶液的部分成分,此时可通过反向荧光相关光谱法(iFCS)对其进行分析。iFCS不需要对NPs或分子进行标记。然而,溶液信号需要浓度为μm - mm的荧光团。在此,我们转而使用来自普通水分子的相干反斯托克斯拉曼散射(CARS)作为溶液信号。通过这种完全无标记的方法,即基于反向CARS的相关光谱法(iCARS - CS),可以分析直径为十分之几纳米且浓度为pM的NPs,并确定它们的绝对体积/浓度。同样,通过利用周围水分子的CARS波动,当脂质囊泡扩散/流过检测体积时,也可以对其进行分析。iCARS - CS很可能提供一种广泛适用的无标记表征技术,例如用于生物分子诊断和筛选中的NPs、小脂质外泌体或微粒,并且还可以利用来自除水以外的生物相关介质的CARS信号。