IP Library Granted Patent US 6,919,445
Granted Patent B2
US 6,919,445 · App. 10/441,950 · Granted Jul 19, 2005

Methods of labelling polynucleotides with dibenzorhodamine dyes

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,919,445
App. No.
10/441,950
Granted
Jul 19, 2005
Kind
B2
Abstract

Dibenzorhodamine compounds having the structure are disclosed, including nitrogen- and aryl-substituted forms thereof. In addition, two intermediates useful for synthesizing such compounds are disclosed, a first intermediate having the structure including nitrogen- and aryl-substituted forms thereof, and a second intermediate having the structure including nitrogen- and aryl-substituted forms thereof, wherein substituents at positions C-14 to C18 taken separately are selected from the group consisting of hydrogen, chlorine, fluorine, lower alkyl, carboxylic acid, sulfonic acid, —CH 2 OH, alkoxy, phenoxy, linking group, and substituted forms thereof. The invention further includes energy transfer dyes comprising the dibenzorhodamine compounds, nucleosides labeled with the dibenzorhodamine compounds, and nucleic acid analysis methods employing the dibenzorhodamine compounds.

Claims (16)

1. A method of polynucleotide sequencing comprising the steps of:

forming a mixture of a first, a second, a third, and a fourth class of polynucleotides such that:

each polynucleotide in the first class includes a 3′-terminal dideoxyadenosine and is labeled with a first dye;

each polynucleotide in the second class includes a 3′-terminal dideoxycytidine and is labeled with a second dye;

each polynucleotide in the third class includes a 3′-terminal dideoxyguanosine and is labeled with a third dye; and

each polynucleotide in the fourth class includes a 3′-terminal dideoxythymidine and is labeled with a fourth dye;

wherein at least one of the first, second, third, or fourth dyes is a dibenzorhodamine compound comprising the structure

including nitrogen- and aryl-substituted forms thereof;

the other of the dyes being spectrally resolvable from the dibenzorhodamine dye(s) and from each other;

electrophoretically separating the polynucleotides thereby forming bands of similarly sized polynucleotides;

illuminating the bands with an illumination beam capable of causing the dyes to fluoresce; and

identifying the classes of the polynucleotides in the bands by the fluorescence spectrum of the dyes.

2. The method of claim 1 , wherein the step of electrophoretically separating is carried out in an electrophoretic matrix is uncrosslinked polyacrylamide or crosslinked polyacrylamide.

3. The method of claim 1 , wherein the uncrosslinked polyacrylamide or crosslinked polyacrylamide has a concentration of from 2-20 weight percent.

4. The method of claim 1 , wherein the uncrosslinked polyacrylamide or crosslinked polyacrylamide concentration is from 4-8 weight percent.

5. The method of claim 1 , wherein the electrophoretic matrix comprises a denaturing agent selected from urea and formamide.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE THE RECEIVING PARTY NAME, PREVIOUSLY RECORDED ON REEL 030182 FRAME 0677. ASSIGNOR(S) HEREBY CONFIRMS THE THE RELEASE OF SECURITY INTEREST. Recorded Mar 4, 2016
From: BANK OF AMERICA, N.A.
To: APPLIED BIOSYSTEMS, LLC
Reel/Frame 037998/0507 →
LIEN RELEASE Recorded Apr 9, 2013
From: BANK OF AMERICA, N.A.
To: APPLIED BIOSYSTEMS, INC.
Reel/Frame 030182/0677 →
SECURITY AGREEMENT Recorded Dec 5, 2008
From: APPLIED BIOSYSTEMS, LLC
To: BANK OF AMERICA, N.A, AS COLLATERAL AGENT
Reel/Frame 021976/0001 →