Inverse-fluorescence correlation spectroscopy: more information and less labeling.
نویسندگان
چکیده
Inverse-Fluorescence Correlation Spectroscopy (iFCS) is a recently developed modification of standard FCS that allows analysis of particles and biomolecules without labeling. The particles generate no signal; instead the signal is generated by a surrounding medium. Particles diffusing through the FCS-detection volume displace a fraction of the surrounding medium, causing transient dips in the detected signal. These give information about the mobility and concentration of the analyzed particles. Also labeled particles can be analyzed, whereby their signal is cross-correlated with that from the surrounding medium (iFCCS). This can give information about the volume of the labeled particles, or alternatively about the size of the detection volume. Also the interaction of unlabeled particles with small, labeled ligands can be analyzed with iFCCS. This allows using cross-correlation as a sensitive indication of binding, even though only one binding-partner is labeled. This review describes the principles of iFCS and iFCCS and measurements of microspheres dissolved in a surrounding medium containing alexa 488. We also discuss practical considerations, and future possibilities for analyses of biomolecules.
منابع مشابه
Comparison of different fluorescence fluctuation methods for their use in FRET assays: monitoring a protease reaction.
We compare the accuracy of a variety of Fluorescence Fluctuation Spectroscopy (FFS) methods for the study of Förster Resonance Energy Transfer (FRET) assays. As an example, the cleavage of a doubly labeled, FRET-active peptide substrate by the protease Trypsin is monitored and analyzed using methods based on fluorescence intensity, Fluorescence Correlation Spectroscopy (FCS) and Fluorescence In...
متن کاملFluctuations as a source of information in fluorescence microscopy
Fluctuations in fluorescence spectroscopy and microscopy have traditionally been regarded as noise—they lower the resolution and contrast and do not permit high acquisition rates. However, fluctuations can also be used to gain additional information about a system. This fact has been exploited in single-point microscopic techniques, such as fluorescence correlation spectroscopy and analysis of ...
متن کاملScanning inverse fluorescence correlation spectroscopy.
Scanning Inverse Fluorescence Correlation Spectroscopy (siFCS) is introduced to determine the absolute size of nanodomains on surfaces. We describe here equations for obtaining the domain size from cross- and auto-correlation functions, measurement simulations which enabled testing of these equations, and measurements on model surfaces mimicking membranes containing nanodomains. Using a confoca...
متن کاملIn vitro study of drug-protein interaction using electronic absorption, fluorescence, and circular dichroism spectroscopy
In the near future, design of a new generation of drugs targeting proteins will be required. Considering the complex bond between the drug and protein, the structure and stability of the target protein should be considered. So far, a series of in vitro investigations have been conducted with the aim of predicting drug-biological medium interactions. In these studies, use of spectroscopic method...
متن کاملProtein–protein interaction analysis by C-terminally specific fluorescence labeling and fluorescence cross-correlation spectroscopy
Here, we describe novel puromycin derivatives conjugated with iminobiotin and a fluorescent dye that can be linked covalently to the C-terminus of full-length proteins during cell-free translation. The iminobiotin-labeled proteins can be highly purified by affinity purification with streptavidin beads. We confirmed that the purified fluorescence-labeled proteins are useful for quantitative prot...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Frontiers in bioscience
دوره 3 شماره
صفحات -
تاریخ انتشار 2011