Sequence-specific affinity precipitation of oligonucleotide using poly(N-isopropylacrylamide)-oligonucleotide conjugate.

In this study we develop a sequence-specific precipitation separation system of oligonucleotide (ODN) using a conjugate between poly(N-isopropylacrylamide) (PNIPAM) and ODN. PNIPAM is known as a thermoresponsive polymer and dehydrates to precipitate above its phase transition temperature in an aqueous milieu. The principal advantage of this separation system using the conjugate is that the hybridization reaction between the conjugate and oligonucleotide is conducted in homogeneous solution. The conjugate was prepared by copolymerization between N-isopropylacrylamide and a vinyl-derivatized (dT)(8). The obtained conjugate efficiently precipitated (dA)(8) from solution when the solution contained more than 1.5 M NaCl. The conjugate containing 3 nmol of (dT)(8) residue was able to precipitate 1.4 nmol of (dA)(8), suggesting that the (dT)(8) residue of the conjugate formed a triple helix with (dA)(8). From an equimolar mixture of (dA)(8) and its one point mutant, the conjugate selectively precipitated (dA)(8): the highest selectivity was obtained for the isolation of (dA)(8) from the mixture consisting of (dA)(4)dT(dA)(3) and (dA)(8). When the conjugate was applied for the precipitation of five oligo(dA)s having different chain lengths, the longer oligo(dA)s tended to be precipitated by the conjugate more efficiently than the shorter ones. The conjugate could be used repeatedly for precipitation of (dA)(8) without showing any loss in precipitation efficiency.

[1]  M. Maeda,et al.  Water-soluble conjugate of double-stranded DNA and Poly(N-isopropylacrylamide) for one-pot affinity precipitation separation of DNA-binding proteins. , 1998, Bioconjugate chemistry.

[2]  T. Okano,et al.  Temperature-responsive bioconjugates. 3. Antibody-poly (N-isopropylacrylamide) conjugates for temperature-modulated precipitations and affinity bioseparations. , 1994, Bioconjugate chemistry.

[3]  M. Rougée,et al.  Sequence specificity in triple-helix formation: experimental and theoretical studies of the effect of mismatches on triplex stability. , 1991, Biochemistry.

[4]  E. Kawashima,et al.  The use of synthetic oligonucleotides as hybridization probes. II. Hybridization of oligonucleotides of mixed sequence to rabbit beta-globin DNA. , 1981, Nucleic acids research.

[5]  J. Bantle,et al.  Specificity of oligo (dT)-cellulose chromatography in the isolation of polyadenylated RNA. , 1976, Analytical biochemistry.

[6]  C. Miyamoto,et al.  Application of oligo(dT)30-latex for rapid purification of poly(A)+ mRNA and for hybrid subtraction with the in situ reverse transcribed cDNA. , 1993, Biochimica et biophysica acta.

[7]  C R Cantor,et al.  Sequence-specific DNA purification by triplex affinity capture. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Shozaburo Saito,et al.  Effect of Additives on Phase Transition of N-Isopropylacrylamide Gels , 1992 .

[9]  Charles R. Cantor,et al.  Oligonucleotide interactions. III. Circular dichroism studies of the conformation of deoxyoligonucleolides , 1970 .

[10]  Kumar,et al.  Affinity precipitation of alpha-amylase inhibitor from wheat meal by metal chelate affinity binding using cu(II)-loaded copolymers of 1-vinylimidazole with N-isopropylacrylamide , 1998, Biotechnology and bioengineering.

[11]  M. Maeda,et al.  Temperature-Induced Precipitation of Specific DNA Fragments Using DNA-Poly(N-isopropylacrylamide) Conjugate , 1999 .

[12]  Hayashida,et al.  Selective Isolation of DNA or RNA Using Single-Stranded DNA Affinity Latex Particles. , 1996, Journal of colloid and interface science.

[13]  Howard G. Schild,et al.  Microcalorimetric detection of lower critical solution temperatures in aqueous polymer solutions , 1990 .

[14]  Tanner Nk Purifying RNA by column chromatography. , 1989 .

[15]  A. Hoffman,et al.  Graft copolymers that exhibit temperature-induced phase transitions over a wide range of pH , 1995, Nature.

[16]  M. Akashi,et al.  Effects of salt on the temperature and pressure responsive properties of poly(N-vinylisobutyramide) aqueous solutions , 1998 .

[17]  A S Hoffman,et al.  Polymer-protein conjugates. II. Affinity precipitation separation of human immunogammaglobulin by a poly(N-isopropylacrylamide)-protein A conjugate. , 1990, Biomaterials.

[18]  Y. Chemla,et al.  Isolation of poly(A)+ RNA by paper affinity chromatography. , 1984, Analytical biochemistry.

[19]  E. Hornes,et al.  Magnetic DNA hybridization properties of oligonucleotide probes attached to superparamagnetic beads and their use in the isolation of poly(A) mRNA from eukaryotic cells. , 1990, Genetic analysis, techniques and applications.

[20]  Jan Feijen,et al.  Effect of comonomer hydrophilicity and ionization on the lower critical solution temperature of N-isopropylacrylamide copolymers , 1993 .

[21]  J. Luong,et al.  Syntheses and applications of water‐soluble reactive polymers for purification and immobilization of biomolecules , 1989, Biotechnology and bioengineering.

[22]  H. Handa,et al.  DNA-carrying latex particles for DNA diagnosis 2. Distinction of normal and point mutant DNA using S1 nuclease , 1998 .

[23]  C L Cooney,et al.  Purification of plasmids by triplex affinity interaction. , 1998, Nucleic acids research.

[24]  H. G. Schild Poly(N-isopropylacrylamide): experiment, theory and application , 1992 .

[25]  U. Lindberg,et al.  Isolation of mRNA from KB-cells by affinity chromatography on polyuridylic acid covalently linked to Sepharose. , 1972, European journal of biochemistry.