Amplification of nucleic acids with electronic detection

• US 7,090,804 B2
• Filed: 01/27/1999
• Issued: 08/15/2006
• Est. Priority Date: 01/27/1998
• Status: Expired due to Fees

• Current Assignee: Osmetech Technology Inc. (Roche Holding AG)
• Original Assignee: Clinical Micro Sensors Incorporated
• Inventors: Kayyem, Jon Faiz, Bamdad, Cynthia
• Primary Examiner(s): Marschel, Ardin H.
• Application Number:
  US09/238,351
• Publication Number:
  US 20020006643A1
• Time in Patent Office: 2,757 Days
• Field of Search: 422/68.1, 435/6, 435/91.1, 435/91.2, 436/501, 536/23.1, 536/22.1, 536 241- 2433, 536/29.3
• US Class Current: 422/68.1
• CPC Class Codes: B01D 17/0214 with removal of one of the phases
• CPC Class Codes: B01D 17/045 with coalescers
• CPC Class Codes: B01D 24/105 downward filtration without specifications about the filter material supporting means
• CPC Class Codes: B01D 24/4642 with valves, e.g. rotating valves
• CPC Class Codes: B01D 24/48 integrally combined with devices for controlling the filtration
• CPC Class Codes: B01D 35/12 Devices for taking out of action one or more units of multi- unit filters, e.g. for regeneration
• CPC Class Codes: B82Y 15/00 Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: C02F 1/283 using coal, charred products, or inorganic mixtures containing them
• CPC Class Codes: C12Q 1/6825 Nucleic acid detection involving sensors
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 2525/113 incorporating modified backbone
• CPC Class Codes: C12Q 2525/313 Branched oligonucleotides
• CPC Class Codes: C12Q 2565/101 Interaction between at least two labels
• CPC Class Codes: C12Q 2565/607 being a sensor, e.g. electrode
• CPC Class Codes: G01N 27/3277 being a redox reaction, e.g. detection by cyclic voltammetry voltammetry per se G01N27/42, G01N27/48

Abstract

The invention relates to compositions and methods useful in the detection of nucleic acids using a variety of amplification techniques, including both signal amplification and target amplification. Detection proceeds through the use of an electron transfer moiety (ETM) that is associated with the nucleic acid, either directly or indirectly, to allow electronic detection of the ETM using an electrode.

Claims

1. A kit for the detection of an amplification reaction of a plurality of target nucleic acid sequences comprising at least a first and a second target sequence, wherein said first and second target sequences are different, said kit comprising:

a) a first nucleic acid primer substantially complementary to at least a first domain of said first target sequence;

b) a first label probe substantially complementary to at least a second domain of said first target sequence, said first label probe comprising a plurality of electron transfer moieties (ETM);

c) a second nucleic acid primer substantially complementary to at least a first domain of said second target sequence;

d) a second label probe substantially complementary to at least a second domain of said second target sequence, said second label probe comprising a plurality of electron transfer moieties (ETM); and

,

e) a substrate comprising at least a first and a second electrode, wherein said first electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a first capture probe substantially complementary to a domain of said first target sequence, and

wherein said second electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a second capture probe substantially complementary to a domain of said second target sequence.

3. A kit according to claim 1, further comprising a thermostable polymerase.

8. A kit according to claim 1, 2, 3, 4, 5, 6, or 7 wherein said first SAM-forming species comprises insulators.

9. A kit according to claim 8, wherein said insulators comprise alkyl chains.

10. A kit according to claim 1, 2, 3, 4, 5, 6, or 7 wherein said first SAM-forming species comprises conductive oligomers.

11. A kit according to claim 1, 2, 3, 4, 5, 6, or 7 wherein said capture probe further comprises an attachment linker.

12. A kit according to claim 11, wherein said attachment linker comprises insulators.

13. A kit according to claim 12, wherein said attachment linker comprises conductive oligomers.

14. A kit according to claim 1, 2, 3, 4, 5, 6, or 7 wherein said ETM is a transition metal complex.

15. A kit according to claim 1, 2, 3, 4, 5, 6, or 7 wherein said ETM is a organic ETM molecule.

16. A kit according to claim 1, 2, 3, 4, 5, 6, or 7 wherein said ETM is a metallocene.

17. A kit according to claim 16, wherein said metallocene is a ferrocene.

18. A kit according to claim 1, 2, 3, 4, 5, 6, or 7 further comprising dNTPs.

2. A kit for the detection of a PCR amplification reaction of a plurality of target nucleic acid sequences comprising at least a first and a second target sequence, wherein said first and second target sequences are different, said kit comprising:

a) a first pair of PCR primers for the amplification of said first target sequence;

b) a first label probe which is substantially complementary to at least a first domain of said first target sequence, wherein said label probe comprises a plurality of electron transfer moieties (ETM);

c) a second pair of PCR primers for the amplification of said second target sequence;

d) a second label probe which is substantially complementary to at least a first domain of said second target sequence, wherein said label probe comprises a plurality of electron transfer moieties (ETM); and

,

e) a substrate comprising at least a first and a second electrode, wherein said first electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a first capture probe substantially complementary to a domain of said first target sequence, and

wherein said second electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a second capture probe substantially complementary to a domain of said second target sequence.

7. A kit according to claim 2, further comprising a thermostable polymerase.

4. A kit for the detection of a LCR amplification reaction of a plurality of target nucleic acid sequences comprising at least a first and a second target sequence, wherein said first and second target sequences are different, said kit comprising:

a) a first nucleic acid primer substantially complementary to at least a first domain of said first target sequence;

b) a second nucleic acid primer substantially complementary to at least a first domain of said second target sequence;

c) a first label probe substantially complementary to a first domain of said first nucleic acid primer, wherein said label probe comprises a plurality of electron transfer moieties (ETM);

d) a second label probe substantially complementary to a first domain of said second nucleic acid primer, wherein said label probe comprises a plurality of electron transfer moieties (ETM);

e) a ligase; and

,

f) a substrate comprising at least a first and a second electrode, wherein said first electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a first capture probe substantially complementary to a domain of said first target sequence, and

wherein said second electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a second capture probe substantially complementary to a domain of said second target sequence.

5. A kit for the detection of a strand displacement amplification (SDA) reaction of a plurality of target nucleic acid sequences comprising at least a first and a second target sequence, wherein said first and second target sequences are different, said kit comprising:

a) a first nucleic acid primer substantially complementary to at least a first domain of said first target sequence;

b) a second nucleic acid primer substantially complementary to at least a first domain of said second target sequence;

c) a polymerase that will modify said first and second nucleic acid primers;

d) a nicking enzyme;

e) a first label probe substantially complementary to a first domain of said first nucleic acid primer, wherein said label probe comprises a plurality of electron transfer moieties (ETM);

f) a second label probe substantially complementary to a first domain of said second nucleic acid primer, wherein said label probe comprises a plurality of electron transfer moieties (ETM); and

,

g) a substrate comprising at least a first and a second electrode, wherein said first electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a first capture probe substantially complementary to a domain of said first target sequence, and

wherein said second electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a second capture probe substantially complementary to a domain of said second target sequence.

6. A kit for the detection of a NASBA amplification reaction of a plurality of target nucleic acid sequences comprising at least a first and a second target sequence, wherein said first and second target sequences are different, said kit comprising:

a) a first nucleic acid primer substantially complementary to at least a first domain of said first target sequence;

b) a second nucleic acid primer substantially complementary to at least a first domain of said second target sequence;

c) a reverse transcriptase,

d) a RNA degrading enzyme,

e) a DNA polymerase;

f) a RNA polymerase;

g) a first label probe substantially complementary to a first domain of said first nucleic acid primer, wherein said label probe comprises a plurality of electron transfer moieties (ETM);

h) a second label probe substantially complementary to a first domain of said second nucleic acid primer, wherein said label probe comprises a plurality of electron transfer moieties (ETM); and

,

i) a substrate comprising at least a first and a second electrode, wherein said first electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a first capture probe substantially complementary to a domain of said first target sequence, and

wherein said second electrode comprises a self-assembled mixed monolayer (SAM) comprising a first SAM-forming species and a second SAM-forming species comprising a second capture probe substantially complementary to a domain of said second target sequence.