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Assay methods and systems

a technology applied in the field of assay methods and systems, can solve the problems of reducing the ability of fluorescent components to emit depolarized fluorescence, and affecting the polarization of fluorescent emissions

Inactive Publication Date: 2004-03-25
CAPLIPER LIFE SCI INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This approach enables efficient detection of reactions by quantifying the reaction progress through changes in fluorescent polarization, enhancing assay efficiency and reducing the need for complex separation procedures.

Problems solved by technology

The preferential association of the large polyionic compound with either the substrate or the product results in a substantial difference in the level of polarization of fluorescent emissions from that component when it is excited using polarized light.
However, association of a large polyionic compound with a small fluorescent molecule will significantly slow the rate of rotational diffusion of that molecule, and reduce its ability to emit depolarized fluorescence.
Typically, this means that the nucleic acid analog will be substantially uncharged, e.g., having insufficient charge to interact with the polyion.
However, due to the flexible nature of nucleic acids, as well as the only incremental increase in size of the hybrid over that of the target, this reduction may not be substantial, and may not be easily detectable.
However, this type of material flow through the intersection would result in a substantial amount of diffusion at the intersection, resulting from both the natural diffusive properties of the material being transported in the medium used, as well as convective effects at the intersection.

Method used

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  • Assay methods and systems
  • Assay methods and systems
  • Assay methods and systems

Examples

Experimental program
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Effect test

example 1

Detection of Phosphorylated Product by Fluorescent Polarization

[0124] An aliquot of a neutrally charged phosphorylatable substrate (Flourescein-QSPKKG-CONH.sub.2) (SEQ. ID NO. 12) was incubated overnight with ATP and CDK2 (cyclin dependent kinase). The mixture was analyzed by standard capillary electrophoresis methods and showed complete conversion of substrate to product. A negative control (no enzyme) was also prepared. The two reaction mixtures were diluted in 50 mM TAPS pH 9.0 buffer (1:40). The fluorescence polarization values were measured by exciting the samples at 490 nm and measuring emitted fluorescence at 520 nm in a cuvette of a fluorimeter equipped to measure fluorescence polarization. Aliquots of a poly-D-Lysine solution and water were added (each added aliquot increased the poly-D-Lysine concentration by 6 .mu.M). The results of the assay are illustrated in FIG. 12A which plots the fluorescent polarization of the sample versus the amount of poly-D-lysine added.

[0125] ...

example 2

Differentiation of Product Concentrations Using Fluorescence Polarization

[0127] Additional experiments were carried out using poly-histidine in place of polylysine. In this case, the buffer used was 50 mM BisTris pH 6.5; the molecular weight of the polyhistidine used was 15800 daltons (available from Sigma Chemical, St. Louis, Mo.).

[0128] Mixtures containing varying ratios of the substrates and products of two serine / threonine kinases were prepared, CDK2 and Protein Kinase A (PKA). The CDK substrate was the same as that described for Example 1, above. The PKA substrate was: Fluor-LRRASLG (SEQ. ID NO. 14) where the C-terminus was either a carboxyl group or a carboxamide group. These mixtures were used as models for kinase reactions at varying degrees of substrate conversion. To these mixtures of substrate and product were added aliquots of a polyhistidine solution and water. The concentration of this aqueous stock was approximately 1.3 mM, and the final concentration was between 10 a...

example 3

Time Course Monitoring of Enzyme Reactions by Fluorescence Polarization

[0132] Another PKA assay was performed with varying concentrations of ATP (0 .mu.M, 0.5 .mu.M, 1 .mu.M, 2 .mu.M, 4 .mu.M, 8 .mu.M, 16 .mu.M and 32 .mu.M) in 50 mM HEPES, pH 7.5, 10 mM MgCl.sub.2, 500 nM polyarginine, 184 nM PKA, and 125 nM Kemptide substrate (Fl-LRRASLG-COO.sup.-) (SEQ. ID NO. 14). The resulting assays were monitored over time in order to determine the efficacy of the fluorescence polarization detection methods of the present invention on monitoring reaction time courses. FIG. 16 is a plot of fluorescence polarization vs. reaction time for each different concentration of ATP in the reaction mix. As can be seen, increasing concentrations of ATP generally give faster reaction rates. In all cases except the control, fluorescence polarization measurements increase with time. In particular, as the reactions progress, more of the fluorescent substrate is rendered charged by virtue of the added phosphat...

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Abstract

Methods, systems, kits for carrying out a wide variety of different assays that comprise providing a first reagent mixture which comprises a first reagent having a fluorescent label. A second reagent is introduced into the first reagent mixture to produce a second reagent mixture, where the second reagent reacts with the first reagent to produce a fluorescently labeled product having a substantially different charge than the first reagent. A polyion is introduced into at least one of the first and second reagent mixtures, and the fluorescent polarization in the second reagent mixture relative to the first reagent mixture is determined, this fluorescent polarization being indicative of the rate or extent of the reaction.

Description

CROSS-REFERENCE TO RELAED APPLICATIONS[0001] This application is a continuation of U.S. patent application Ser. No. 10 / 057,812, filed Jan. 24, 2002, which is a continuation of U.S. patent application Ser. No. 09 / 727,532, filed Nov. 28, 2000 (now U.S. Pat. No. 6,436,646), which is a continuation of U.S. patent application Ser. No. 09 / 569,193, filed May 11, 2000 (now U.S. Pat. No. 6,472,141), which is a continuation-in-part of U.S. patent application Ser. No. 09 / 316,447, filed May 21, 1999 (now U.S. Pat. No. 6,287,774), and also claims priority to Provisional Patent Application Nos. 60 / 139,562, filed Jun. 16, 1999 and 60 / 156,366, filed Sep. 28, 1999. The disclosure of each of these references is incorporated by reference in its entirety for all purposes.[0002] Virtually all chemical, biological and biochemical research depends upon the ability of the investigator to determine the direction of her research by assaying reaction mixtures for the presence or absence of a particular chemic...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12N15/09G01N21/64C12Q1/37C12Q1/42C12Q1/48C12Q1/68G01N21/78G01N33/53G01N33/542G01N33/566
CPCC12Q1/37C12Q1/42C12Q1/48C12Q1/6816G01N33/542G01N2333/9121C12Q2565/107C12Q2563/107C12Q2563/137C12Q2561/119
Inventor NIKIFOROV, THEO T.
Owner CAPLIPER LIFE SCI INC
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