Enzymatic time-resolved luminescent assay for nucleic acids quantitation

• US 8,206,905 B2
• Filed: 04/26/2008
• Issued: 06/26/2012
• Est. Priority Date: 04/26/2008
• Status: Expired due to Fees

• Current Assignee: Valeri Golovlev, Ye Sun
• Original Assignee: Valeri Golovlev, Ye Sun
• Inventors: Golovlev, Valeri, Sun, Ye
• Primary Examiner(s): Babic, Christopher M.
• Application Number:
  US12/110,297
• Publication Number:
  US 20090317803A1
• Time in Patent Office: 1,522 Days
• Field of Search: None
• US Class Current: 435/6.1
• CPC Class Codes: C12Q 1/66 involving luciferase

Abstract

The objects of the present invention are to provide a new technology platform for quantitation number of copies of nucleic acid molecules of interest by lumonogenic (i.e., enzymatic luminescence) detection. The detection approach of the method of present invention is essentially employing time-resolved approach, e.g., based on detection transient parameters of luminescent signal. The various disclosed embodiments allow DNA and RNA quantification in a broad dynamic range; can be used for detection of DNA, as well as long (mRNA) and short (microRNA) RNA targets. The present invention provides methods, instruments, and kits for fast and highly sensitive identification and measurements of nucleic acids in various life science and biomedical applications.

Claims

1. A method of quantitation of inorganic pyrophosphate in a sample, comprising:

a) obtaining at least one sample suspected of containing inorganic pyrophosphate molecules;

b) adding pyrophosphate detection solution to said sample, wherein said pyrophosphate detection solution utilizes ATP sulfurylase, 5′

-phosphosulphate (APS), luciferin-luciferase and inorganic pyrophosphatase (PPase);

c) detecting intensity of luminescent light vs, time from said sample with said pyrophosphate detection solution added;

d) measuring amplitudes of the rising and decaying components of said luminescent intensity vs. time;

e) calculating the amount of inorganic pyrophosphate and ATP present in said sample, wherein the amount of pyrophosphate is proportional to the rising component of luminescent intensity vs. time and the amount of ATP is proportional to the difference between the rising and decaying component of the luminescent signal.

2. The method of claim 1, wherein inorganic pyrophosphate is generated by a nucleic acid replication reaction.

3. The method of claim 2, wherein the nucleic acid replication reaction is carried out in presence of dideoxynucleotides.

4. The method of claim 1, wherein inorganic pyrophosphate is generated by a nucleic acid replication reaction and wherein said reaction is carried out in presence of an inhibitor of the nucleic acid replication reaction.