Method of analysis of samples by determination of a function of specific brightness
A method for characterizing samples having units, by monitoring fluctuating intensities of radiation emitted, scattered and/or reflected by said units in at least one measurement volume, the monitoring being performed by at least one detection means, said method comprising the steps of: a) measuring in a repetitive mode a number of photon counts per time interval of defined length, b) determining a function of the number of photon counts per said time interval, c) determining a function of specific brightness of said units on basis of said function of the number of photon counts.
1. A method for analyzing a sample involving detecting radiation from particles or molecules in a measurement volume of the sample, the method comprising the steps of:
measuring by detection means, in a repetitive mode, a number of photon counts per time interval of defined length,
determining an experimental distribution function of the number of photon counts measured per time interval,
determining a distribution function of specific brightness of the particles or molecules based on the experimental distribution function of the number of photon counts measured, by fitting an expected distribution function of the number of photon counts against the experimental distribution function of photon counts, wherein the expected distribution function of the number of photon counts is calculated using characteristics of a spatial brightness function, employing values of volumes of sections of the measurement volume corresponding to a selected set of values of the spatial brightness function and considering the volumes as variables depending on modeling parameters of the spatial brightness function, and selecting the values of these modeling parameters which yield the closest fit between the experimentally determined and the expected distribution of the number of photon counts.
2. The method according to claim 1 , wherein radiation from particles or molecules in one or more measurement volume(s) is measured.
3. The method according to claim 1 , wherein the detection means is part of a confocal microscopic set-up further having:
at least one microscope objective having an image plane for both focusing an incident laser beam and collecting radiation emitted, scattered and/or reflected by the particles or molecules of the sample,
a dichroic mirror,
a pinhole in the image plane of the microscope objective,
and data acquisition means.
4. The method according to claim 3 , wherein dimensions of the pinhole are used as a modeling parameter of the spatial brightness function.
5. The method according to claim 3 , wherein the incident laser beam has a convergence angle used as a modeling parameter of the spatial brightness function.
6. The method according to claim 3 , wherein the confocal microscopic set-up further comprises means for scanning and/or moving the sample.
7. The method according to claim 3 , wherein the at least one microscope objective has a numerical aperture=0.9.
8. The method according to claim 1 , wherein the particles are molecular aggregates, complexes, vesicles, cells, viruses, bacteria, beads, or mixtures thereof in solids, liquids or gases.
9. The method according to claim 1 , wherein the particles or molecules can be grouped into species distinguished by their specific brightness.
10. The method according to claim 9 , wherein at least one of the species is luminescent.
11. The method according to claim 9 , wherein at least one of the species is luminescently labeled.
12. The method according to claim 9 , wherein at least one of the species is fluorescent.
13. The method according to claim 1 , wherein the particles carry binding sites for luminescent molecules.
14. The method according to claim 2 , wherein the sample has a volume, and the measurement volume is less than the volume of the sample.
15. The method according to claim 14 , wherein the measurement volume is ≦10 −12 1.
16. The method according to claim 14 , wherein the particles or molecules move into and out of the measurement volume during measuring.
17. The method according to claim 14 , wherein the particles or molecules are optically scanned.
18. The method according to claim 2 , wherein the measurement volumes are arranged two-dimensionally.
19. The method according to claim 18 , wherein the measurement volumes are arranged on a membrane or a sheet having wells.
20. The method according to claim 2 , wherein the measurement volume is restricted by the use of elements of near field optical microscopy, or elements of near field optical microscopy in combination with conventional microscopy optics.