Do you want to publish a course? Click here

Robustness of FCS (Fluorescence Correlation Spectroscopy) with Quenchers Present

102   0   0.0 ( 0 )
 Added by Steve Granick
 Publication date 2019
  fields Physics
and research's language is English




Ask ChatGPT about the research

Inspired by recent publications doubtful of the FCS technique, we scrutinize how irreversible (static) and reversible (dynamic) quenching can influence the interpretation of such data. We consider intermediate cases where the assessment of photophysics (static quenching, blinking-like triplet state relaxation) influence on autocorrelation curves can be delicate if dye-labeled objects diffuse on comparably-rapid time scales and use tryptophan as the quencher. As our example of small-molecule dye that diffuses rapidly, we mix quencher with Alexa 488 dye, and quenching is reflected in the fact that the data become exceptionally noisy. This reflects the bidisperse population of quenched and unquenched dye when the time scales overlap between the processes of translational diffusion, quenching, and blinking. As our example of large-molecule dye-labeled object, we mixed quencher with dye-labeled bovine serum albumin. Diffusion, static quenching and blinking time scales are now separated, and inferred translational diffusion now depends weakly on quencher. We conclude that when the diffusing molecule is substantially slower to diffuse than the time scale of photophysical processes of the fluorescent dye to which it is attached, influence of quenching is self-evident and the FCS autocorrelation curves give appropriate diffusion coefficient if correct fitting functions are chosen in the analysis.



rate research

Read More

We discuss the manner in which the dynamics of tracer polystyrene chains varies with the concentration of matrix polystyrene chains dissolved in toluene. Using fluorescence correlation spectroscopy and theory, it is shown that the cooperative diffusion coefficient of the matrix polystyrene chains can be measured by fluorescence correlation spectroscopy in the semidilute entangled concentration regime. In addition the self-diffusion coefficient of the tracer polystyrene chains can be detected for arbitrary concentrations. The measured cooperative diffusion coefficient is independent of the molecular weight of the tracer polystyrene chains because it is a characteristic feature of the transient entanglement network.
We present a comprehensive investigation of polymer diffusion in the semidilute regime by fluorescence correlation spectroscopy (FCS) and dynamic light scattering (DLS). Using single-labeled polystyrene chains, FCS leads to the self-diffusion coefficient while DLS gives the cooperative diffusion coefficient for exactly the same molecular weights and concentrations. Using FCS we observe a new fast mode in the semidilute entangled concentration regime beyond the slower mode which is due to self-diffusion. Comparison of FCS data with data obtained by DLS on the same polymers shows that the second mode observed in FCS is identical to the cooperative diffusion coefficient measured with DLS. An in-depth analysis and a comparison with current theoretical models demonstrates that the new cooperative mode observed in FCS is due to the effective long-range interaction of the chains through the transient entanglement network.
We introduce an elegant method which allows the application of diffusing-wave spectroscopy (DWS) to nonergodic, solid-like samples. The method is based on the idea that light transmitted through a sandwich of two turbid cells can be considered ergodic even though only the second cell is ergodic. If absorption and/or leakage of light take place at the interface between the cells, we establish a so-called multiplication rule, which relates the intensity autocorrelation function of light transmitted through the double-cell sandwich to the autocorrelation functions of individual cells by a simple multiplication. To test the proposed method, we perform a series of DWS experiments using colloidal gels as model nonergodic media. Our experimental data are consistent with the theoretical predictions, allowing quantitative characterization of nonergodic media and demonstrating the validity of the proposed technique.
We report results of direct measurements of velocity profiles in a microchannel with hydrophobic and hydrophilic walls, using a new high precision method of double-focus spacial fluorescence cross-correlation under a confocal microscope. In the vicinity of both walls the measured velocity profiles do not turn to zero by giving a plateau of constant velocity. This apparent slip is proven to be due to a Taylor dispersion, an augmented by shear diffusion of nanotracers in the direction of flow. Comparing the velocity profiles near the hydrophobic and hydrophilic walls for various conditions shows that there is a true slip length due to hydrophobicity. This length, of the order of several tens of nanometers, is independent on electrolyte concentration and shear rate.
We demonstrate a simple technique to measure the resonant frequency of the 398.9 nm 1S0 - 1P1 transition for the different Yb isotopes. The technique, that works by observing and aligning fluorescence spots, has enabled us to measure transition frequencies and isotope shifts with an accuracy of 60 MHz. We provide wavelength measurements for the transition that differ from previously published work. Our technique also allows for the determination of Doppler shifted transition frequencies for photoionisation experiments when the atomic beam and laser beam are not perpendicular and furthermore allows us to determine the average velocity of the atoms along the direction of atomic beam.
comments
Fetching comments Fetching comments
Sign in to be able to follow your search criteria
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا