System and method for performing polynucleotide separations using liquid chromatography

Abstract

Improved liquid chromatography systems having components made of titanium, stainless steel, or organic polymeric material are useful in the separation of polynucleotide fragments, particularly large fragments of double-stranded polynucleotides, by Matched Ion Polynucleotide Chromatography (MIPC). The titanium, stainless steel, or polymeric components are treated so that they do not release multivalent cations into aqueous solutions flowing through the chromatography system. Alternatively, or in addition to utilizing materials made of the components listed above, a multivalent cation capture resin placed upstream of the separation column can be employed to remove multivalent ions from the system. The multivalent cation capture resin can be contained in a guard disk, a guard column, or a guard cartridge. Novel methods for separating mixtures of polynucleotide fragments into fractions based on their molecular weight by Matched Ion Polynucleotide Chromatography and slalom chromatography utilize the liquid chromatographic systems described above.

What is claimed is:  
     
         1 . A method for separating a mixture of polynucleotide fragments during passage through a liquid chromatographic column containing a separation bed comprising Matched Ion Polynucleotide Chromatography separation particles, wherein the method comprises supplying and feeding solutions entering the column with components having process solution-contacting surfaces which contact process solutions held therein or flowing therethrough, wherein said process solution-contacting surfaces are material which does not release multivalent cations into aqueous solutions held therein or flowing therethrough, whereby the column is protected from multivalent cation contamination of the contents thereof, and wherein the polynucleotide fragments are separated by Matched Ion Polynucleotide Chromatography.  
     
     
         2 . The method of  claim 1  wherein said polynucleotide fragments are separated based on the size of said polynucleotide fragments.  
     
     
         3 . The method of  claim 1  wherein said polynucleotide fragments are separated based on the polarity of said polyucleotide fragments.  
     
     
         4 . The method of  claim 1 , wherein said surfaces are comprised of material selected from the group consisting of titanium, coated stainless steel, and organic polymer.  
     
     
         5 . The method of  claim 1 , wherein said surfaces have been subjected to a multivalent cation removal treatment.  
     
     
         6 . The method of  claim 5  wherein said treatment comprises contacting said surfaces with an aqueous solution containing a member selected from the group consisting of nitric acid, phosphoric acid, pyrophosphoric acid, and chelating agents.  
     
     
         7 . The method of  claim 1 , wherein said particles have been subjected to an acid wash treatment.  
     
     
         8 . The method of  claim 1  wherein said process solutions include a mobile phase additive present in sufficient amount to capture multivalent cation contaminants.  
     
     
         9 . The method of  claim 1  wherein said additive is an agent selected from the group consisting of EDTA and crown ethers.  
     
     
         10 . The method of  claim 1  including degassing means for removing oxygen from said process solutions.  
     
     
         11 . The method of  claim 1 , wherein multivalent cations in mobile phase solutions and sample solutions entering the column are removed by contacting said solutions with multivalent cation capture resin before said solutions enter the column to protect the separation bed from multivalent cation contamination, wherein said multivalent capture resin is selected from cation exchange resin and chelating resin.  
     
     
         12 . The method of  claim 11 , wherein said multivalent cation capture resin is cation exchange resin having an ion exchange moiety selected from the group consisting of iminodiacetate, nitriloacetate, acetylacetone, arsenazo, hydroxypyridinone, and 8-hydroxyquinoline groups.  
     
     
         13 . The method of  claim 11 , wherein said ion exchange moiety is an iminodiacetate group.  
     
     
         14 . The method of  claim 1 , wherein the polynucleotide fragments are double-stranded.  
     
     
         15 . The method of  claim 1 , wherein the polynucleotide fragments comprise  5  or more base pairs.  
     
     
         16 . The method of  claim 1 , wherein said separation particles comprise alkylated non-porous polymer beads having an average diameter of about 1-100 microns.  
     
     
         17 . The method of  claim 1 , wherein said separation particles comprise poly(styrene-divinylbenzene) beads having an average diameter of about 1-100 microns.  
     
     
         18 . A method for separating a mixture of polynucleotide fragments during passage through a liquid chromatographic column containing a separation bed comprising Matched Ion Polynucleotide Chromatography separation particles, wherein multivalent cations in process solutions entering the column are removed by contacting said solutions with multivalent cation capture resin selected from cation exchange resin and chelating resin before said solutions enter the column to protect the separation bed from multivalent cation contamination, and wherein the polynucleotide fragments are separated by Matched Ion Polynucleotide Chromatography, wherein the method further comprises supplying and feeding solutions entering the column with components having process solution-contacting surfaces which contact process solutions held therein or flowing therethrough, and wherein said process solution-contacting surfaces are material which does not release multivalent cations into process solutions held therein or flowing therethrough.  
     
     
         19 . The method of  claim 18 , wherein said surfaces are comprised of material selected from the group consisting of titanium, coated stainless steel, and organic polymer.  
     
     
         20 . The method of  claim 18 , wherein said surfaces have been subjected to a multivalent cation removal treatment.  
     
     
         21 . The method of  claim 20  wherein the treatment comprises contacting said surfaces with an aqueous solution containing a member selected from the group consisting of nitric acid, phosphoric acid, pyrophosphoric acid, and chelating agents.  
     
     
         22 . The method of  claim 18  wherein said process solutions include a mobile phase additive present in sufficient amount to capture multivalent cation contaminants.  
     
     
         23 . The method of  claim 22  wherein said additive is comprised of an agent selected from the group consisting of EDTA and crown ethers.  
     
     
         24 . The method of  claim 18  including degassing means for removing oxygen from said process solutions.  
     
     
         25 . The method of  claim 18 , wherein the polynucleotide fragments are double-stranded.  
     
     
         26 . The method of  claim 18 , wherein the polynucleotide fragments comprise  5  or more base pairs.  
     
     
         27 . A method for separating a mixture of polynucleotide fragments during passage through a liquid chromatographic column containing a separation bed comprising Matched Ion Polynucleotide Chromatography separation particles, wherein the method comprises supplying and feeding solutions entering the column with components having process solution-contacting surfaces which contact process solutions held therein or flowing therethrough, wherein said process solution-contacting surfaces are material which does not release multivalent cations into aqueous solutions held therein or flowing therethrough, whereby the column is protected from multivalent cation contamination of the contents thereof, wherein the polynucleotide fragments are separated by Matched Ion Polynucleotide Chromatography, wherein said process solutions include a mobile phase additive present in sufficient amount to capture essentially any multivalent cation contaminants, and wherein said additive is comprised of EDTA.