IP Library Granted Patent US 7,393,640
Granted Patent B2
US 7,393,640 · App. 10/772,996 · Granted Jul 1, 2008

Terminal-phosphate-labeled nucleotides with new linkers

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Quick Facts
Patent No.
US 7,393,640
App. No.
10/772,996
Granted
Jul 1, 2008
Kind
B2
Abstract

The present invention describes methods of using terminal-phosphate-labeled nucleotides in the presence of a manganese salt to enhance their substrate properties towards various enzymes. Particularly described are methods of detecting a nucleic acid in a sample, based on the use of terminal-phosphate-labeled nucleotides as substrates for nucleic acid polymerases, in the presence of a manganese salt. Further provided are manganese complexes of terminal-phosphate-labeled nucleotides as well as terminal-phosphate-labeled nucleotides with new linkers with enhanced substrate properties.

Claims (13)

1. A method of increasing the rate of an enzyme catalyzed nucleoside monophosphate transfer from a terminal-phosphate-labeled nucleoside polyphosphate to detect the activity of said enzyme or said terminal-phosphate-labeled nucleoside polyphosphate, said method comprising:

a) conducting said enzyme catalyzed nucleoside monophosphate transfer from a terminal-phosphate-labeled nucleoside polyphosphate reaction in reaction buffer comprising a manganese salt, thereby increasing the rate of said reaction over the rate of said reaction in the absence of manganese;

wherein said enzyme is a template dependent DNA polymerase,

further wherein said reaction is conducted in a template dependent manner.

2. The method of claim 1 , wherein the polymerase is selected from Phi 29 DNA polymerase, Klenow exo - , T7 DNA polymerase exo - , Taq DNA polymerase, Taq F667Y deletion 1-235 DNA polymerase, Thermus thermophilus F667Y D18A DNA polymerase, Taq F667Y D18A E681M DNA polymerase, T. hypogea (Thy B) DNA polymerase, T. neapolitana (Tne) DNA polymerase, T. subterranea (Tsu) DNA polymerase, T. barossii (Tba) DNA polymerase, T. litoralis DNA polymerase, T. kodakaraensis DNA polymerase, P. furiosis DNA polymerase, P. GB-D DNA polymerase, Human Pol beta, Tsp JS1, AMV-reverse transcriptase, MMLV-reverse transcriptase and HIV-reverse transcriptase.

3. The method of claim 1 , wherein the concentration of manganese salt is at least 0.01 mM.

4. The method of claim 1 , wherein the manganese salt concentration is between 0.01 to 50 mM.

5. The method of claim 1 , wherein the manganese salt concentration is between 0.1 to 10 mM.

6. The method of claim 1 , wherein an additional metal salt other than manganese, is also present with the terminal-phosphate labeled nucleoside polyphosphate.

7. The method of claim 6 , wherein said additional metal salt is a magnesium or a calcium salt.

8. The method of claim 6 , wherein said additional metal salt is present at a concentration of 0.01 mM to 50 mM.

9. The method of claim 1 , further comprising conducting said reaction in the presence of a metal ion buffer to modulate the concentration of free metal ion.

10. The method according to claim 9 , wherein said metal ion buffer is a dicarboxylic acid.

Assignments (2)
CHANGE OF NAME Recorded Aug 31, 2020
From: GE HEALTHCARE BIO-SCIENCES CORP.
To: GLOBAL LIFE SCIENCES SOLUTIONS USA LLC
Reel/Frame 053648/0854 →
CHANGE OF NAME Recorded Feb 6, 2006
From: AMERSHAM BIOSCIENCES CORP
To: GE HEALTHCARE BIO-SCIENCES CORP.
Reel/Frame 017125/0266 →