Luminescence assay using cyclical excitation wavelength sequence

• US 6,444,476 B1
• Filed: 02/26/2001
• Issued: 09/03/2002
• Est. Priority Date: 05/29/1998
• Status: Expired due to Fees

• Current Assignee: Photonic Research Systems Limited
• Original Assignee: Photonic Research Systems Limited
• Inventors: Morgan, Christopher Grant
• Primary Examiner(s): SNAY, JEFFREY R
• Application Number:
  US09/701,471
• Time in Patent Office: 554 Days
• Field of Search: 436/536, 436/537, 436/546, 436/805, 436/172, 435/6, 422/82.07, 422/82.08, 250/452.1, 250/459.1
• US Class Current: 436/172
• CPC Class Codes: G01N 2021/6441 with two or more labels
• CPC Class Codes: G01N 21/6408 with measurement of decay time, time resolved fluorescence
• 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

Abstract

A method for the conduct of a measurement of proximity between luminescent species based on detection of transfer of excitation energy between them. A first photoluminescent species (the “donor”) and a second photoluminescent species (the “acceptor”) are provided and are such that the donor species and the acceptor species have at least some excitation spectral regions which differ and that at least a part of the emission spectrum of the donor overlaps with at least a part of the excitation spectrum of the acceptor. The donor species is excited with a cyclical temporal sequence of wavelength bands, optionally provided as pulses or modulated in intensity, giving rise to a characteristic temporal fluctuation in emission therefrom and emission in at least one wavelength band characteristic of the acceptor is analyzed to detect the presence of the said characteristic fluctuation or a subcomponent thereof and optionally also to detect a fluctuation characteristic of direct excitation of the acceptor.

Claims

1. A method of effecting measurement of proximity between luminescent species based on detection of transfer of excitation energy therebetween, the method comprising providing a first photoluminescent species (the ‘

donor’

) and a second photoluminescent species (the ‘

acceptor’

) which are such that the donor species and the acceptor species have at least some excitation spectral regions which differ and also such that at least a part of the emission spectrum of the donor overlaps with at least a part of the excitation spectrum of the acceptor,

exciting the donor species with an excitation source, and

analyzing emission of the acceptor using a detection means,

characterized in that the donor species is excited with a cyclical temporal sequence of wavelength bands, optionally provided as pulses or modulated in intensity, giving rise to a characteristic temporal fluctuation in emission from the donor species, and

emission in at least one wavelength band characteristic of the acceptor is analyzed to detect the presence of the said characteristic fluctuation or a subcomponent thereof and optionally also to detect a fluctuation characteristic of direct excitation of the acceptor.

2. A method according to claim 1 wherein luminescence is also measured in a spectral region characteristic of donor emission and a temporal fluctuation characteristic of the donor is detected.

3. A method according to claim 1 wherein excitation wavelengths are scanned cyclically in a continuous or discrete manner across the excitation maximum of the donor at a first scanning frequency and luminescence is detected at one temporal frequency or more that is an integral multiple of the said scanning frequency.

4. A method according to claim 3 wherein the excitation wavelengths are each programmed in intensity so as to concentrate detected signal in a given harmonic of the cyclic scanning frequency.

5. A method according to claim 1 wherein the excitation source is a plurality of light-emitting diodes, operated individually or in groups in a programmed sequence and with a programmed intensity.

6. A method according to claim 1 wherein the excitation source comprises a plurality of light sources coupled to a fibre-optic light guide or liquid light guide.

7. A method according to claim 6 wherein the light sources are based on plasma emission from excited hydrogen, deuterium, mercury, xenon or other element.

8. A method according to claim 1 wherein the excitation source illuminates a sample in a ‘

dark-field’

configuration such that the sample is excited obliquely or with a hollow cone of light illuminating a given region in space and wherein the said region is viewed by one or more detection means at an angle or angles chosen to minimize direct exposure of the said detection means to the exciting radiation.

9. A method according to claim 1 wherein the detection means is equipped with a tunable wavelength-selective filter and this is scanned cyclically across at least a part of the emission band of the acceptor species giving rise to a characteristic temporal fluctuation in detected signal therefrom, and the superposition of the said fluctuation and that due to the cyclic variation of excitation wavelength is measured to detect the joint fluctuation or characteristic temporal components thereof.

10. A method according to claim 1 wherein the detection means is equipped with a tunable optical filter comprising or containing a liquid-crystalline medium, an acousto-optic tunable filter, a tunable Fabry-Perot cavity filter, an interference filter tuned by tilting from the optical axis or a filter based on wavelength-dependent scattering from particles in a medium, such as a Christiansen filter.

11. A method according to claim 1 wherein the detection means is an imaging detector.

12. A method according to claim 11 wherein the detection means can be gated or modulated in sensitivity and where such gating or modulation is used to facilitate selective detection of emission from one or more of the donor and acceptor.

13. A method according to claim 1 wherein the excitation of the donor species is by simultaneous or sequential absorption of two or more photons of the same or different wavelength.

14. A method according to claim 13 wherein the donor species is an upconversion medium based on direct or sensitized excitation of emissive species within a supporting matrix.

15. A method according to any preceding claim wherein the excitation means is driven to produce pulsed or modulated light and a measurement is made by time-domain or frequency-domain methods to detect a signal jointly on the basis of the emissive lifetime of one or more of the donor and acceptor and of the temporal fluctuations in detected emission resulting from either or both of the cyclic variation of excitation wavelength and the cyclic variation of optical wavelengths passed to the detector.

16. A method according to claim 15 wherein the donor has an emissive lifetime at least threefold longer than that of the acceptor.

17. A method according to claim 15 wherein the acceptor has an emissive lifetime at least threefold longer than the donor.