Polynucleotide capture materials, and methods of using same

• US 8,324,372 B2
• Filed: 07/11/2008
• Issued: 12/04/2012
• Est. Priority Date: 07/13/2007
• Status: Active Grant

• Current Assignee: HandyLab Incorporated (Becton, Dickinson & Co)
• Original Assignee: HandyLab Incorporated (Becton, Dickinson & Co)
• Inventors: Brahmasandra, Sundaresh N., Craig, Elizabeth
• Primary Examiner(s): Crane, Lawrence E
• Application Number:
  US12/172,214
• Publication Number:
  US 20090131650A1
• Time in Patent Office: 1,607 Days
• Field of Search: None
• US Class Current: 536/25.4
• CPC Class Codes: C07C 233/36 having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
• CPC Class Codes: C07H 1/08 from natural products
• CPC Class Codes: C08G 83/003 Dendrimers
• CPC Class Codes: C12N 15/1013 by using magnetic beads
• CPC Class Codes: C12Q 1/6813 Hybridisation assays

Abstract

Methods for processing polynucleotide-containing biological samples, and materials for capturing polynucleotide molecules such as RNA and/or DNA from such samples. The RNA and/or DNA is captured by polyamidoamine (PAMAM(Generation 0)) bound to a surface, such as the surface of magnetic particles. The methods and materials have high efficiency of binding RNA and of DNA, and of release, and thereby permit quantitative determinations.

Claims

1. A method for isolating polynucleotides in a cell-containing sample from a polymerase chain reaction inhibitor selected from the group consisting of hemoglobin, peptides, faecal compounds, humic acids, mucousal compounds, DNA binding proteins, and saccharides, or any combination thereof, the method comprising:

contacting the sample with a lysis solution containing a lysis reagent, said lysis reagent comprising a detergent, and a plurality of binding particles, wherein the binding particles comprise PAMAM(Generation

     0) covalently bound to the surface of the binding particles, said lysis solution having a pH between 4 and 8;

heating the sample contacted with the lysis reagent, thereby lysing cells contained in the sample in the lysis solution and concomitantly binding the polynucleotides to the PAMAM of the binding particles to create binding particles bound with polynucleotides and a remaining residual solution;

compacting the binding particles bound with polynucleotides by bringing the binding particles bound with polynucleotides in contact with one another;

removing a substantial portion of the residual solution; and

contacting the compacted binding particles with a release solution having a pH of ≧

9, thereby releasing the polynucleotides from the PAMAM of the binding particles.

2. The method of claim 1, wherein the polynucleotides comprise DNA, and wherein the release solution has a pH of ≧

12.

3. The method of claim 1, wherein the polynucleotides comprise RNA, and wherein the release solution has a pH of ≧

9.

4. The method of claim 1, wherein the polynucleotides have a size less than 7.5 Mbp.

5. The method of claim 1, wherein the binding particles are a polymeric material, further wherein said polymeric material is selected from the group consisting of:

polystyrene, latex polymers, polyacrylamide, and polyethylene oxide.

6. The method of claim 5, further wherein the polymeric material comprises one or more carboxylic groups to which the PAMAM(Generation 0) is covalently linked.

7. The method of claim 1, wherein the particles have an average diameter of between about 0.5 microns and about 10 microns.

8. The method of claim 1, wherein the particles are present in a density of about 10⁷-10⁹ particles per milliliter.

9. The method of claim 1, wherein at least some of the particles are magnetic.

10. The method of claim 1, wherein the step of heating the sample contacted with the lysis reagent comprises incubating the sample with the lysis reagent and the particles at 60°

C. for 5-10 minutes.

11. The method of claim 1, wherein the step of heating the sample contacted with the lysis reagent comprises incubating the sample with the lysis reagent and the particles between room temperature and 60°

C.

12. The method of claim 1, wherein the polynucleotides comprise a mixture of DNA and RNA molecules, the method comprising contacting the binding particles bound by polynucleotides successively with a first release solution having a pH in the range 9-12, followed by a second release solution having a pH in the range 12-14.

13. The method of claim 1, wherein the method does not comprise centrifugation of the particles.

14. The method of claim 1, wherein the time required for completing the contacting, compacting, removing, and releasing is between 10 and 30 minutes.

15. The method of claim 1, wherein the sample has a volume larger than the concentrated volume of the binding particles having the polynucleotides bound thereto by a factor of at least about 10.

16. The method of claim 1, further comprising neutralizing the release solution containing the polynucleotides with a buffered neutralizing solution, thereby producing a solution of PCR-ready polynucleotides.

17. The method of claim 1, further comprising contacting the binding particles with a wash solution prior to releasing the polynucleotides from the binding particles into the release solution, wherein the wash solution is a buffered solution having a pH less than 8.5.

18. A method for concentrating RNA from a sample containing polymerase chain reaction inhibitors, the method comprising:

contacting between 500 μ

l and 1 ml of the sample with a plurality of RNA binding particles, wherein the binding particles retain the RNA in the sample as compared to the polymerase chain reaction inhibitors;

magnetically compacting the plurality of binding particles having the one or more polynucleotides bound thereto into an effective volume between 50 nanoliters and 5 microliters; and

releasing the one or more polynucleotides into <

30 μ

l of a release solution comprising a buffered solution having a pH≧

9.

19. A composition comprising:

carboxyl modified microparticles; and

PAMAM(Generation

     0) covalently bound via one or more amine groups per molecule to one or more of the carboxylic acid groups on the microparticles.