One-step procedure for the purification of nucleic acids

Abstract

The present invention is a new and non-obvious method for the improved and simplified purification of nucleic acids.

What is claimed is: 
     
         1 ) A method of removing lysis buffer components from a nucleic acid sample, the method comprising
 a) providing a specimen comprising or suspected of comprising nucleic acids,   b) contacting the specimen with one or more lysis reagents,   c) contacting the specimen with a solid substrate for a length of time and under conditions suitable for nucleic acids in the specimen to bind to the solid substrate and   d) causing the solid substrate bound with nucleic acids, if nucleic acid is present in the specimen, to pass through an aqueous-based separation gel.   
     
     
         2 ) The method of  claim 1 , wherein the lysis buffer contains salts in a concentration greater than about 1 molar. 
     
     
         3 ) The method of  claim 1 , wherein the solid substrate is a microparticle. 
     
     
         4 ) The method of  claim 3 , wherein the solid substrate is a microparticle from about 0.1 nm to about 5 nm in diameter. 
     
     
         5 ) The method of  claim 4 , wherein the solid substrate is a microparticle from about 0.8 nm to about 5 nm in diameter. 
     
     
         6 ) The method of  claim 3 , wherein the microparticle is magnetic. 
     
     
         7 ) The method of  claim 1 , wherein the nucleic acids bound to the solid substrate are contacted with an elution buffer after passing through the aqueous gel which elutes nucleic acids from the solid substrate. 
     
     
         8 ) The method of  claim 7 , wherein the method does not include precipitation of the nucleic acids in an organic solvent. 
     
     
         9 ) The method of  claim 7 , wherein the method does include precipitation of the nucleic acids in an organic solvent and the organic solvent is ethanol. 
     
     
         10 ) The method of  claim 3 , wherein the nucleic acids bound to the solid substrate are contacted with an enzyme after passing through the aqueous gel. 
     
     
         11 ) The method of  claim 10 , wherein the enzyme is a DNA polymerase or a reverse transcriptase. 
     
     
         12 ) The method of  claim 10 , wherein the nucleic acid is sequenced on the solid substrate without dilution. 
     
     
         13 ) The method of  claim 3 , wherein the nucleic acids bound to the solid substrate are contacted with bisulfite after passing through the aqueous gel such that unmethylated cytosines are deaminated. 
     
     
         14 ) The method of  claim 13 , further comprising determining whether at least one nucleic base in the nucleic acid has an epigenetic modification. 
     
     
         15 ) The method of  claim 1 , wherein the nucleic acid is bound to the solid substrate via an entity selected from the group consisting of nucleic acid hybridization, an aptamer, an antibody, an antibody fragment, biotin, avidin, and streptavidin. 
     
     
         16 ) A method for enriching nucleic acids from a sample, the method comprising:
 a) providing;
 i) a sample suspected of comprising nucleic acids, 
 ii) microparticles suitable for binding nucleic acids, and 
 iii) an aqueous-based separation gel, 
   b) contacting the sample with the microparticles for a length of time and under conditions suitable for any nucleic acids in the sample to bind to the magnetic microparticles to create loaded magnetic microparticles;   c) drawing the loaded microparticles through the aqueous-based separation gel with a magnetic field.   
     
     
         17 ) The method of  claim 16 , wherein said separating gel comprises agarose. 
     
     
         18 ) The method of  claim 17 , wherein said agarose is at a concentration of about 0.10% to about 1.0%. 
     
     
         19 ) The method of  claim 17 , wherein said separating gel also comprises one of more of ethanol and glycerol. 
     
     
         20 ) The method of  claim 16 , wherein said particles comprise a functional group suitable for binding nucleic acid. 
     
     
         21 ) The method of  claim 16 , wherein said microparticles are magnetic. 
     
     
         22 ) The method of  claim 21 , wherein said magnetic microparticles are at least partly coated with one or more of silica and glass. 
     
     
         23 ) The method of  claim 21 , wherein said magnetic microparticles are spheroid. 
     
     
         24 ) The method of  claim 16 , wherein said sample comprises lysis buffer.