Compositions, methods, kits and apparatus for determining the presence or absence of target molecules

• US 6,001,570 A
• Filed: 02/18/1997
• Issued: 12/14/1999
• Est. Priority Date: 02/18/1997
• Status: Expired due to Fees

• Current Assignee: Oligomerix, Inc.
• Original Assignee: Invitro Diagnostics Incorporated
• Inventors: Grossman, Abraham
• Primary Examiner(s): Houtteman, Scott W.
• Application Number:
  US08/801,154
• Time in Patent Office: 1,029 Days
• Field of Search: 435/6, 435/91.2, 435/91.21, 435/91.31, 536/24.3
• US Class Current: 435/5
• CPC Class Codes: C12Q 1/6862 Ligase chain reaction [LCR]
• CPC Class Codes: C12Q 1/6867 Replicase-based amplification, e.g. using Q-beta replicase
• CPC Class Codes: C12Q 2531/137 Ligase Chain Reaction [LCR]
• CPC Class Codes: C12Q 2531/149 Replicase based amplification, e.g. Q beta replicase

Abstract

The present invention is directed to methods, compositions, kits and apparatus; to identify and detect the presence or absence of target analytes. The embodiments of the present invention have utility in medical diagnosis and analysis of various chemical compounds in specimens and samples, as well as the design of test kits and apparatus for implementing such methods.

Claims

1. A first ribonucleic acid (RNA) molecule and a second RNA molecule for use in determining the presence or absence of a target molecule, said first RNA molecule capable of binding to a target molecule and having the following formula:

space="preserve" listing-type="equation">5'"'"'-A-B-C-3'"'"';

wherein A is a section of the RNA molecule having 10-100,000 nucleotides which section is capable of being received by an RNA replicase and with another RNA sequence, F, being replicated and the letter "B" denotes a section of the RNA molecule having approximately 10 to 50,000 nucleotides which section is capable of binding to the target molecule and the letter "C" denotes a section of the RNA molecule having approximately 1 to 10,000 nucleotides which section is capable of being ligated to another RNA sequence, "D";

said second RNA molecule capable of binding to said target molecule and having the following formula;

space="preserve" listing-type="equation">5'"'"'-D-E-F-3'"'"';

wherein D is a section of the RNA molecule having approximately 1 to 10,000 nucleotides which section is capable being ligated with another RNA sequence, "C", and the letter "E" denotes a section of the RNA molecule having approximately 10 to 100,000 nucleotides which section is capable of binding to the target molecule, and the letter "F" denotes a section of the RNA molecule having 10 to 100,000 nucleotides which section is capable of being received by an RNA replicase and with another sequence, "A", being replicated;

said first and the second RNA molecules are capable of forming a third RNA molecule having the following formula;

space="preserve" listing-type="equation">5'"'"'-A-B-C-D-E-F-3'"'"';

said third RNA molecule formed by ligating the C and D sections, as the E and the B sections are bound to target, said third RNA molecule capable of being received by an RNA replicase and being replicated by such enzyme as a indication of the presence or absence ol the target molecule.

2. The RNA molecules of claim 1 wherein said sequences represented by the letters "A" and "F" are selected from the group of sequences consisting of MDV-I RNA, Q-beta RNA microvariant RNA, nanovariant RNA, midivariant RNA and modifications of such sequences which maintain the ability of the sequences to be replicated by Q-beta replicase.

3. The RNA molecules of claim 1 wherein the sections B and E bind to the target through non-nucleic acid pairing interactions.

4. The RNA molecules of claim 1 wherein the B and E sections are aptamers or partial aptamers.

5. The RNA molecules of claim 1 wherein the sections C and D together define a site for ligation.

6. A kit for determining the presence or absence of a target molecule comprising a first ribonucleic acid (RNA) molecule and a second RNA, ligase means and amplification means, said first RNA molecule capable of binding to a target molecule and having the following formula:

space="preserve" listing-type="equation">5'"'"'-A-B-C-3'"'"';

wherein A is a section of the RNA molecule having 10 to 100,000 nucleotides which section is capable of being received by an RNA replicase and with another RNA sequence, F, being replicated and the letter "B" denotes a section of the RNA molecule having approximately 10 to 50,000 nucleotides, which section is capable of binding to the target molecule, and the letter "C" denotes a section of the RNA molecule having approximately 1 to 10,000 nucleotides, which section is capable of being ligated to another RNA sequence, "D";

said second RNA molecule capable of binding to said target molecule and having the following formula;

space="preserve" listing-type="equation">5'"'"'-D-E-F-3'"'"';

wherein D is a section of the RNA molecule having approximately 1 to 10,000 nucleotides which section is capable being ligated to another RNA sequence, "C", and the letter "E" denotes a section of the RNA molecule having approximately 10 to 50,000 nucleotides which section is capable of binding to the target molecule, and the letter "F" denotes a section of the RNA molecule having 10 to 100,000 nucleotides which section is capable of being received by an RNA replicase and with another sequence, "A", being replicated;

said first and the second RNA molecules are capable of forming a third RNA molecule having the following formula;

space="preserve" listing-type="equation">5'"'"'-A-B-C-D-E-F-3'"'"';

said third RNA molecule formed by ligating the C and D sections, as the E and the B sections are bound to target, said third RNA molecule capable of being received by an RNA replicase and being replicated by such enzyme as a indication of the presence or absence of the target molecule;

said ligase means capable of forming said third RNA molecule in the presence of said complex and said amplification means capable of forming a plurality of said third RNA molecule or a corresponding RNA or DNA molecule in the presence of said third molecule.

7. A method of making a first ribonucleic acid (RNA) molecule and a second RNA molecule for use in determining the presence or absence of a target molecule, said first RNA molecule capable of binding to a target molecule and having the following formula:

space="preserve" listing-type="equation">5'"'"'-A-B-C-3'"'"';

wherein A is a section of the RNA molecule having 10-100,000 nucleotides which section is capable of being received by an RNA replicase and with another RNA sequence, F, being replicated and the letter "B" denotes a section of the RNA molecule having approximately 10 to 50,000 nucleotides which section is capable of binding to the target molecule and the letter "C" denotes a section of the RNA molecule having approximately 1 to 10,000 nucleotides which section is capable of being ligated to another RNA sequence, "D";

said second RNA molecule capable of binding to said target molecule and having the following formula;

space="preserve" listing-type="equation">5'"'"'-D-E-F-3'"'"';

wherein D is a section of the RNA molecule having approximately 1 to 10,000 nucleotides which section is capable being ligated with another RNA sequence, "C", and the letter "E" denotes a section of the RNA molecule having approximately 10 to 100,000 nucleotides which section is capable of binding to the target molecule, and the letter "F" denotes a section of the RNA molecule having 10 to 100,000 nucleotides which section is capable of being received by an RNA replicase and with another sequence, "A", being replicated, said first and the second RNA molecules are capable of forming a third RNA molecule having the following formula;

space="preserve" listing-type="equation">5'"'"'-A-B-C-D-E-F-3'"'"';

said third RNA molecule formed by ligating the C and D sections, as the E and the B sections are bound to target, said third RNA molecule capable of being received by an RNA replicase and being replicated by such enzyme as a indication of the presence or absence of the target molecule;

comprising the step of combining a sample containing the target molecule with a library of RNA molecules having the formula;

space="preserve" listing-type="equation">5'"'"'-A-B'"'"'-C-D-E'"'"'-F-3'"'"';

to form a mixture of one or more target bound RNA molecules and one or more unbound RNA molecules, wherein the letters B'"'"' and E'"'"' are sections with randomized nucleotides and represent potential sections B and E;

combining primer nucleic acid corresponding to at least one section with the mixture with an enzyme capable of degrading the unbound RNA molecules and imposing conditions for degradation;

releasing said bound RNA molecules from target; and

amplifying said bound RNA molecules with an RNA replicase to form an amplification product having the formula;

space="preserve" listing-type="equation">5'"'"'-A-B'"'"'-C-D-E'"'"'-F-3'"'"';

cleaving said amplification product to form the first and second RNA molecules.

8. The method of claim 7 wherein said sections B'"'"' and E'"'"' are randomized nucleotide sequences.

9. A kit for performing the method of claim 7 comprising one or more sections of the third RNA molecule and an amplification enzyme.

10. A first ribonucleic acid (RNA) molecule and a second RNA molecule for use in determining the presence or absence of a target molecule, said first RNA molecule capable of binding to a target molecule and having the following formula:

space="preserve" listing-type="equation">5'"'"'-A-B-C-3'"'"';

wherein A is a section of the RNA molecule having 10-100,000 nucleotides which section is capable of being received by an RNA replicase and with another RNA sequence, F, being replicated and the letter "B" denotes a section of the RNA molecule having approximately 10 to 50,000 nucleotides which section is capable of binding to the target molecule through non-Watson-Crick binding and the letter "C" denotes a section of the RNA molecule having approximately 1 to 10,000 nucleotides which section is capable of being ligated to another RNA sequence, "D", with an RNA ligase;

said second RNA molecule capable of binding to said target molecule and having the following formula;

space="preserve" listing-type="equation">5'"'"'-D-E-F-3'"'"';

wherein D is a section of the RNA molecule having approximately 1 to 10,000 nucleotides which section is capable being ligated with another RNA sequence, "C" with an RNA ligase, and the letter "E" denotes a section of the RNA molecule having approximately 10 to 100,000 nucleotides which section is capable of binding to the target molecule through non-Watson-Crick binding, and the letter "F" denotes a section of the RNA molecule having 10 to 100,000 nucleotides which section is capable of being received by an RNA replicase and with another sequence, "A", being replicated;

said first and the second RNA molecules are capable of forming a third RNA molecule having the following formula;

space="preserve" listing-type="equation">5'"'"'-A-B-C-D-E-F-3'"'"';

said third RNA molecule formed by ligating the C and D sections, as the E and the B sections are bound to target, said third RNA molecule capable of being received by an RNA replicase and being replicated by such enzyme as a indication of the presence or absence of the target molecule.