US5538848A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Method for detecting nucleic acid amplification using self-quenching fluorescence probe
Assignee: Applied Biosystems LLC
•
Filing: 1994-11-16
•
Granted: 1996-07-23
•
Expires: 2014-11-16
Abstract
Abstract A method is provided for monitoring the progress of nucleic acid amplifications that rely on a nucleic acid polymerase having 5'->3' exonuclease activity. An important feature of the method is providing an oligonucleotide probe having a reporter molecule and a quencher molecule at either end such that the quencher molecule substantially quenches any fluorescence from the reporter whenever the oligonucleotide probe is in a single stranded state and such that the reporter is substantially unquenched whenever the oligonucleotide probe is in a double stranded state hybridized to a target polynucleotide.
Inventors
- 👤 Kenneth J. Livak
- 👤 Susan J. A. Flood
- 👤 Jeffrey Marmaro
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-28 16:52
CPC Classifications
C; C12; C12Q; C12Q1/00; C12Q1/68; C12Q1/6813; C12Q1/6816; C12Q1/6818; C12Q1/6834; C12Q1/6837
Claims Analysis
Total Claims: 27
Claim 1
Independent Claim
183 words
A method for monitoring nucleic acid amplification comprising: performing nucleic acid amplification on a target polynucleotide using a nucleic acid polymerase having 5'-3' nuclease activity, a primer capable of hybridizing to said target polynucleotide, and an oligonucleotide probe capable of hybridizing to said target polynucleotide, 3' relative to said primer, said oligonucleotide probe having a fluorescent reporter molecule and a quencher molecule capable of quenching the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one single-stranded conformation when unhybridized where said quencher molecule quenches the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one conformation when hybridized to said target polynucleotide where the fluorescence of said reporter molecule is unquenched, the fluorescence intensity of said reporter molecule being greater than the fluorescence intensity of said quencher molecule when said probe is hybridized to said target; polynucleotide, said nucleic acid polymerase digesting said oligonucleotide probe during amplification to separate said reporter molecule from said quencher molecule; and monitoring the fluorescence of said reporter molecule, the generation of fluorescence corresponding to the occurrence of nucleic acid amplification.
Claim 2
Independent Claim
183 words
A method for monitoring nucleic acid amplification comprising: performing nucleic acid amplification on a target polynucleotide using a nucleic acid polymerase having 5'-3' nuclease activity, a primer capable of hybridizing to said target polynucleotide, and an oligonucleotide probe capable of hybridizing to said target polynucleotide, 3' relative to said primer, said oligonucleotide probe having a fluorescent reporter molecule and a quencher molecule capable of quenching the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one single-stranded conformation when unhybridized where said quencher molecule quenches the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one conformation when hybridized to said target polynucleotide where the fluorescence of said reporter molecule is unquenched, the fluorescence intensity of said reporter molecule being greater than the fluorescence intensity of said quencher molecule when said probe is hybridized to said target; polynucleotide, said nucleic acid polymerase digesting said oligonucleotide probe during amplification to separate said reporter molecule from said quencher molecule; and monitoring the fluorescence of said reporter molecule, the generation of fluorescence corresponding to the occurrence of nucleic acid amplification.
Claim 3
Dependent Claim
17 words
The method according to claim 1 wherein said nucleic acid polymerase is a thermostable nucleic acid polymerase.
Claim 4
Dependent Claim
22 words
The method according to claim 1 wherein said reporter molecule is a fluorescein dye and said quencher molecule is a rhodemine dye.
Claim 5
Dependent Claim
22 words
The method according to claim 1 wherein said reporter molecule is separated from said quencher molecule by at least about 15 nucleotides.
Claim 6
Dependent Claim
23 words
The method according to claim 3 wherein said reporter molecule is separated from said quencher molecule by between about 15 and 60 nucleotides.
Claim 7
Dependent Claim
22 words
The method according to claim 1 wherein raid reporter molecule is separated from said quencher molecule by at least about 18 nucleotide.
Claim 8
Dependent Claim
23 words
The method according to claim 3 wherein said reporter molecule is separated from said quencher molecule by between about 18 and 30 nucleotides.
Claim 9
Dependent Claim
20 words
The method according to claim 1 wherein the reporter molecule is attached to a 3' terminal nucleotide of the probe.
Claim 10
Dependent Claim
20 words
The method according to claim 8 wherein the quencher molecule is attached to a 5' terminal nucleotide of the probe.
Claim 11
Dependent Claim
20 words
The method according to claim 1 wherein the reporter molecule is attached to a 5' terminal nucleotide of the probe.
Claim 12
Dependent Claim
20 words
The method according to claim 10 wherein the quencher molecule is attached to a 3' terminal nucleotide of the probe.
Claim 13
Dependent Claim
20 words
The method according to claim 1 wherein the quencher molecule is attached to a 3' terminal nucleotide of the probe.
Claim 14
Dependent Claim
19 words
The method according to claim 1 wherein the quencher molecule is attached to 5' terminal nucleotide of the probe.
Claim 15
Independent Claim
193 words
A method for monitoring nucleic acid amplification comprising: performing nucleic acid amplification on a target polynucleotide using a nucleic acid polymerase having 5'-3' nuclease activity, a primer capable of hybridizing to said target polynucleotide, and an oligonucleotide probe capable of hybridizing to said target polynucleotide 3' relative to said primer, said oligonucleotide probe having a fluorescent reporter molecule and a quencher molecule capable of quenching the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one single-stranded conformation when unhybridized where said quencher molecule quenches the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one conformation when hybridized to said target polynucleotide where the fluorescence of said reporter molecule is unquenched the fluorescence intensity of said oligonucleotide probe hybridized to said target polynucleotide being at least about a factor of 6 greater than the fluorescence intensity of said oligonucleotide probe when not hybridized to said target polynucleotide, said nucleic acid polymerase digesting said oligonucleotide probe during amplification to separate said reporter molecule from said quencher molecule; and monitoring the fluorescence of said reporter molecule, the generation of fluorescence corresponding to the occurrence of nucleic acid amplification.
Claim 16
Independent Claim
193 words
A method for monitoring nucleic acid amplification comprising: performing nucleic acid amplification on a target polynucleotide using a nucleic acid polymerase having 5'-3' nuclease activity, a primer capable of hybridizing to said target polynucleotide, and an oligonucleotide probe capable of hybridizing to said target polynucleotide 3' relative to said primer, said oligonucleotide probe having a fluorescent reporter molecule and a quencher molecule capable of quenching the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one single-stranded conformation when unhybridized where said quencher molecule quenches the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one conformation when hybridized to said target polynucleotide where the fluorescence of said reporter molecule is unquenched the fluorescence intensity of said oligonucleotide probe hybridized to said target polynucleotide being at least about a factor of 6 greater than the fluorescence intensity of said oligonucleotide probe when not hybridized to said target polynucleotide, said nucleic acid polymerase digesting said oligonucleotide probe during amplification to separate said reporter molecule from said quencher molecule; and monitoring the fluorescence of said reporter molecule, the generation of fluorescence corresponding to the occurrence of nucleic acid amplification.
Claim 17
Dependent Claim
22 words
The method according to claim 14 wherein said reporter molecule is separated from said quencher molecule by at least about 15 nucleotides.
Claim 18
Dependent Claim
23 words
The method according to claim 15 wherein said reporter molecule is separated from said quencher molecule by between about 15 and 60 nucleotides.
Claim 19
Dependent Claim
20 words
The: method according to claim 14 wherein the reporter molecule is attached to a 3' terminal nucleotide of the probe.
Claim 20
Dependent Claim
20 words
The method according to claim 17 wherein the quencher molecule is attached to a 5' terminal nucleotide of the probe.
Claim 21
Dependent Claim
20 words
The method according to claim 14 wherein the reporter molecule is attached to a 5' Terminal nucleotide of the probe.
Claim 22
Dependent Claim
20 words
The method according to claim 19 wherein the quencher molecule is attached to a 3' terminal nucleotide of the probe.
Claim 23
Dependent Claim
20 words
The method according to claim 14 wherein the quencher molecule is attached to a 5' terminal nucleotide of the probe.
Claim 24
Dependent Claim
20 words
The method according to claim 14 wherein the quencher molecule is attached to a 3' terminal nucleotide of the probe.
Claim 25
Dependent Claim
39 words
The method according to claim 1 wherein the fluorescence intensity of said reporter molecule is at least about a favor 3.5 greater than the fluorescence intensity of said quencher molecule when said probe is hybridized to said target polynucleotide.
Claim 26
Independent Claim
209 words
A method for monitoring nucleic acid amplification comprising: performing nucleic acid amplification on a target polynucleotide using a nucleic acid polymerase having 5'-3' nuclease activity, a primer capable of hybridizing to said target polynucleotide and an oligonucleotide probe capable of hybridizing to said target polynucleotide 3' relative to said primer, said oligonucleotide probe having a fluorescent reporter molecule and a quencher molecule capable of quenching the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one single-stranded conformation when unhybridized where said quencher molecule quenches the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one conformation when hybridized to said target polynucleotide where the fluorescence of said reporter molecule is unquenched, the ratio of the fluorescence intensities of said reporter molecule to said quencher molecule when said probe is hybridized to said target polynucleotide being at least about a factor of 6 greater than the ratio of the fluorescence intensities of said reporter molecule to said quencher molecule when said probe is single-stranded, said nucleic acid polymerase digesting said oligonucleotide probe during amplification to separate said reporter molecule from said quencher molecule; and monitoring the fluorescence of said reporter molecule, the generation of fluorescence corresponding to the occurrence of nucleic acid amplification.
Claim 27
Independent Claim
209 words
A method for monitoring nucleic acid amplification comprising: performing nucleic acid amplification on a target polynucleotide using a nucleic acid polymerase having 5'-3' nuclease activity, a primer capable of hybridizing to said target polynucleotide and an oligonucleotide probe capable of hybridizing to said target polynucleotide 3' relative to said primer, said oligonucleotide probe having a fluorescent reporter molecule and a quencher molecule capable of quenching the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one single-stranded conformation when unhybridized where said quencher molecule quenches the fluorescence of said reporter molecule, said oligonucleotide probe existing in at least one conformation when hybridized to said target polynucleotide where the fluorescence of said reporter molecule is unquenched, the ratio of the fluorescence intensities of said reporter molecule to said quencher molecule when said probe is hybridized to said target polynucleotide being at least about a factor of 6 greater than the ratio of the fluorescence intensities of said reporter molecule to said quencher molecule when said probe is single-stranded, said nucleic acid polymerase digesting said oligonucleotide probe during amplification to separate said reporter molecule from said quencher molecule; and monitoring the fluorescence of said reporter molecule, the generation of fluorescence corresponding to the occurrence of nucleic acid amplification.
References Cited (Backward Citations)
US4220450A
Cited
EP0229943B1
Cited
WO1990003446A1
Cited
WO1992002638A1
Cited
US5210015A
Cited
US5332659A
Cited
EP0601889A2
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1999-07-23 | 2000-01-22 | 2000-07-23 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2003-07-23 | 2004-01-22 | 2004-07-23 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2007-07-23 | 2008-01-22 | 2008-07-23 | $7700.00 | Window Closed / Lapsed |