INCREASED SPECIFICITY OF ANALYTE DETECTION BY MEASUREMENT OF BOUND AND UNBOUND LABELS

• US 20090170070A1
• Filed: 06/07/2007
• Published: 07/02/2009
• Est. Priority Date: 06/15/2006
• Status: Abandoned Application

• Current Assignee: Koninklijke Philips Electronics N.V. (Koninklijke Philips N.V.)
• Original Assignee: Koninklijke Philips Electronics N.V. (Koninklijke Philips N.V.)
• Inventors: Neerken, Sieglinde, Schmidt, Kristiane Anne, Lucassen, Gerhardus Wilhelmus
• Application Number:
  US12/304,564
• Publication Number:
  US 20090170070A1
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms
• CPC Class Codes: G01N 33/582 with fluorescent label

Abstract

The present invention describes the provision of an internal control in analytical techniques involving labeling of analytes, such as SERRS, for detection of an analyte, particularly a biomolecule in a sample, with improved accuracy.

Claims

1. A method for detecting and/or quantifying an analyte in a sample, comprising the steps of:

a) contacting said sample comprising said analyte with a predetermined amount of label capable of binding to said analyte;

b) detecting the fraction of label bound to said analyte;

whereby the amount of label bound to said analyte is indicative of the presence and/or amount of said analyte in said sample; and

c) detecting the fraction of label not bound to said analyte;

whereby the amount of label not bound to said analyte, deducted from said predetermined amount of label, provides an internal control indicative of the presence and/or amount of said analyte in said sample.

wherein said detection step in (b) and (c) is ensured using an optical detection method.

2. The method of claim 1, wherein said detection step (b) and said detection step (c) is performed within the same sample.

3. The method according to claim 1, wherein said detection step in (b) and (c) is ensured using SE(R)RS and wherein said label is a SE(R)RS-active label.

4. The method according to claim 3, further comprising, prior to step (b) and (c), contacting of said fraction of label bound to said analyte and of said fraction of label not bound to said analyte with a SE(R)RS-active surface.

5. The method according to claim 1, wherein said label is an analyte-specific label.

6. The method according to claim 1, wherein said analyte-specific label comprises an analyte-specific probe.

7. The method according to claim 1, wherein said analyte is a nucleotide sequence and said analyte-specific probe is a oligonucleotide having a sequence complementary to a sequence within said analyte.

8. The method according to claim 2, wherein use is made of a label which allows differential detection of said label bound to said analyte and said label which is not bound to said analyte.

9. The method according to claim 1, wherein said label is a fluorescent and/or a SE(R)RS-active label of which the maximum absorption frequency is shifted from a first to a second frequency on association of said fluorescent and/or SE(R)RS-active label with said SE(R)RS-active surface.

10. The method of claim 1, further comprising, prior to step (b) the step of separating the fraction of label bound to said analyte from the fraction of label not bound to said analyte.

11. The method according to claim 10, wherein said separation of said fraction of bound label and said fraction of unbound label is ensured by making use of an analyte-specific probe which is provided with a tag which can be subjected to a physical or chemical force.

12. The method according to claim 10, wherein said label is a SE(R)RS-active label, wherein prior to step (b) and (c) said fraction of label bound to said analyte and said fraction of label not bound to said analyte are contacted with a SE(R)RS-active surface and wherein said separation is ensured by using a SE(R)RS-active surface which functions as or is provided with a tag which can be subjected to a physical or chemical force.

13. A system for detecting and/or quantifying the presence of an analyte in a sample, comprising:

a) means for contacting said sample potentially comprising said analyte with a predetermined amount of label capable of binding to said analyte;

b) means for detecting the fraction of label bound to said analyte;

whereby the amount of label bound to said analyte is indicative of the presence and optionally of the amount of analyte in said sample; and

c) means for detecting the fraction of label not bound to said analyte;

whereby the amount of label not bound to said analyte, deducted from said predetermined amount of label, provides an internal control indicative of the presence and optionally the amount of analyte in said sample,

wherein said detection is ensured using an optical detection method.