Fluorescence interference contrast microscopy


Fluorescence interference contrast microscopy is a microscopic technique developed to achieve z-resolution on the nanometer scale.
FLIC occurs whenever fluorescent objects are in the vicinity of a reflecting surface. The resulting interference between the direct and the reflected light leads to a double sin2 modulation of the intensity, I, of a fluorescent object as a function of distance, h, above the reflecting surface. This allows for the nanometer height measurements.
FLIC microscope is well suited to measuring the topography of a membrane that contains fluorescent
probes e.g. an artificial lipid bilayer, or a living cell membrane or the structure of fluorescently labeled proteins on a surface.

FLIC optical theory

General two layer system

The optical theory underlying FLIC was developed by Armin Lambacher and Peter Fromherz. They derived a relationship between the observed fluorescence intensity and the distance of the fluorophore from a reflective silicon surface.
The observed fluorescence intensity,, is the product of the excitation probability per unit time,, and the probability of measuring an emitted photon per unit time,. Both probabilities are a function of the fluorophore height above the silicon surface, so the observed intensity will also be a function of the fluorophore height. The simplest arrangement to consider is a fluorophore embedded in silicon dioxide a distance d from an interface with silicon. The fluorophore is excited by light of wavelength and emits light of wavelength. The unit vector gives the orientation of the transition dipole of excitation of the fluorophore. is proportional to the squared projection of the local electric field,, which includes the effects of interference, on the direction of the transition dipole.




The local electric field,, at the fluorophore is affected by interference between the direct incident light and the light reflecting off the silicon surface. The interference is quantified by the phase difference given by




is the angle of the incident light with respect to the silicon plane normal. Not only does interference modulate, but the silicon surface does not perfectly reflect the incident light. Fresnel coefficients give the change in amplitude between an incident and reflected wave. The Fresnel coefficients depend on the angles of incidence, and, the indices of refraction of the two mediums and the polarization direction. The angles and can be related by Snell's Law. The expressions for the reflection coefficients are:




TE refers to the component of the electric field perpendicular to the plane of incidence and TM to the parallel component. In cartesian coordinates, the local electric field is




is the polarization angle of the incident light with respect to the plane of incidence. The orientation of the excitation dipole is a function of its angle to the normal and azimuthal to the plane of incidence.




The above two equations for and can be combined to give the probability of exciting the fluorophore per unit time.

Many of the parameters used above would vary in a normal experiment. The variation in the five following parameters should be included in this theoretical description.
The squared projection must be averaged over these quantities to give the probability of excitation. Averaging over the first 4 parameters gives


Normalization factors are not included. is a distribution of the orientation angle of the fluorophore dipoles. The azimuthal angle and the polarization angle are integrated over analytically, so they no longer appear in the above equation. To finally obtain the probability of excitation per unit time, the above equation is integrated over the spread in excitation wavelength, accounting for the intensity and the extinction coefficient of the fluorophore.



The steps to calculate are equivalent to those above in calculating except that the parameter labels em are replaced with ex and in is replaced with out.



The resulting fluorescence intensity measured is proportional to the product of the excitation probability and emission probability


It is important to note that this theory determines a proportionality relation between the measured fluorescence intensity and the distance of the fluorophore above the reflective surface. The fact that it is not an equality relation will have a significant effect on the experimental procedure.

Experimental Setup

A silicon wafer is typically used as the reflective surface in a FLIC experiment. An oxide layer is then thermally grown on top of the silicon wafer to act as a spacer. On top of the oxide is placed the fluorescently labeled specimen, such as a lipid membrane, a cell or membrane bound proteins.
With the sample system built, all that is needed is an epifluorescence microscope and a CCD camera to make quantitative intensity measurements.
. However, depending on the numerical aperture used, the experiment will yield good lateral resolution or good vertical resolution, but not both. A high N.A. gives good lateral resolution which is best if the goal is to determine long range topography. Low N.A., on the other hand, provides accurate z-height measurement to determine the height of a fluorescently labeled molecule in a system.

Analysis

The basic analysis involves fitting the intensity data with the theoretical model allowing the distance of the fluorophore above the oxide surface to be a free parameter.
The FLIC curves shift to the left as the distance of the fluorophore above the oxide increases. is usually the parameter of interest, but several other free parameters are often included to optimize the fit. Normally an amplitude factor and a constant additive term for the background are included. The amplitude factor scales the relative model intensity and the constant background shifts the curve up or down to account for fluorescence coming from out of focus areas, such as the top side of a cell. Occasionally the numerical aperture of the microscope is allowed to be a free parameter in the fitting. The other parameters entering the optical theory, such as different indices of refraction, layer thicknesses and light wavelengths, are assumed constant with some uncertainty.
A FLIC chip may be made with oxide terraces of 9 or 16 different heights arranged in blocks. After a fluorescence image is captured, each 9 or 16 terrace block yields a separate FLIC curve that defines a unique. The average is found by compiling all the values into a histogram.


The statistical error in the calculation of comes from two sources: the error in fitting of the optical theory to the data and the uncertainty in the thickness of the oxide layer. Systematic error comes from three sources: the measurement of the oxide thickness, the fluorescence intensity measurement with the CCD, and the uncertainty in the parameters used in the optical theory. The systematic error has been estimated to be.