Multiple label fluorescence polarization assay system and method

• US 6,566,143 B2
• Filed: 02/26/2001
• Issued: 05/20/2003
• Est. Priority Date: 02/25/2000
• Status: Expired due to Term

• Current Assignee: Cambridge Research & Instrumentation Incorporated (Revvity, Inc.)
• Original Assignee: Cambridge Research & Instrumentation Incorporated (Revvity, Inc.)
• Inventors: Hoyt, Clifford C.
• Primary Examiner(s): Spyrou; Cassandra
• Assistant Examiner(s): Lavarias; Arnel C.
• Application Number:
  US09/794,903
• Publication Number:
  US 20010033374A1
• Time in Patent Office: 813 Days
• Field of Search: 356/317,318,416,417,418,364,365,366,368,369,370 250/458.1,459.1,461.2 436/172 422/82.05,82.08
• US Class Current: 436/172
• CPC Class Codes: G01N 2021/6421 Measuring at two or more wavelengths
• CPC Class Codes: G01N 2021/6441 with two or more labels
• CPC Class Codes: G01N 2021/6471 Special filters, filter wheel
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/6445 Measuring fluorescence polarisation
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates

Abstract

A sample having a plurality of probe molecules is illuminated with at least one beam of excitation light that is linearly polarized along a first axis, thereby effecting fluorescence emission in a plurality of spectral bands. The intensity of a first component of fluorescence emission that is polarized along the first axis, as well as the intensity of a second component of fluorescence emission that is polarized along an orthogonal second axis, is measured for each of said plurality of spectral bands. These measurements are represented as a measurement vector M. Since each probe emits some limited amount of light in the characteristic band of another probe, this results in cross-talk between probes. The measurement vector is therefore corrected using an instrument response matrix A, which is generated by measuring the flux output of control samples which each have only a single probe species. A flux vector S is calculated according to S=A⁻¹M, and the fluorescence polarization FP is calculated from the S values.

Claims

1. A method for measuring the fluorescence polarization of a plurality of probes in a single sample, which method compensates for spectral cross-talk among said plurality of probes, said method comprising

illuminating a sample having a plurality of probes with at least one linearly polarized beam of excitation light, thereby effecting fluorescence emission in a plurality of spectral bands,

measuring the intensity of a first component of fluorescence emission that is linearly polarized along a first axis, in each of said plurality of spectral bands,

measuring the intensity of a second component of fluorescence emission that is linearly polarized along a second axis that is orthogonal to the first axis, in each of said plurality of spectral bands,

illuminating each of a plurality of samples which each have only a respective one of said probes with at least one linearly polarized beams of excitation light, thereby effecting fluorescence emission in at least one of said plurality of spectral bands from each of said plurality of samples,

measuring the intensities of said first and second components of fluorescence emission in each of said plurality of spectral bands for each of said samples which each have only a respective one of said probes, and

compensating for spectral cross-talk amongst said plurality of probes by determining the relative contributions from each of said probes to the measured intensities of said first and second components of fluorescence emission at each spectral band, and calculating the fluorescence polarization of each of said plurality of probes based on said relative contributions.