Separation of nucleotides with an aqueous mobile phase using pH- and temperature-responsive polymer modified packing materials

被引:33
作者
Ayano, E
Sakamoto, C
Kanazawa, H
Kikuchi, A
Okano, T
机构
[1] Kyoritsu Univ Pharm, Dept Phys Pharmaceut Chem, Tokyo 1058512, Japan
[2] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Tokyo 1628666, Japan
关键词
D O I
10.2116/analsci.22.539
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
A new method for the qualitative analysis of adenosine nucleotides (AMP, ADP, and ATP) and synthetic oligonucleotides has been proposed, utilizing a pH- and temperature-responsive polymer of N-isopropylacrylamide (NIPAAm), butyl methacrylate (BMA) and N,N-dimethylaminopropylacrylamide (DMAPAAm) as the stationary phase of HPLC. In the chromatographic system using the copolymer with ionizable groups of modified packing materials, we investigated how to separate adenosine nucleotides and oligonucleotides by temperature. The properties of the surface of the copolymer-grafted stationary phase altered from hydrophilic to hydrophobic and from charged to non-charged due to changes in the temperature and in the pH, respectively. In addition, it is possible to exhibit and hide ion-exchange groups on the polymer chain surface by temperature changes. These phenomena result from changes in the charge and hydrophobicity of the pH- and temperature-responsive polymer on the stationary surface with the controlling temperature. A pH- and temperature-responsive chromatography would be greatly useful for biopolymer and nucleotide separation and purification.
引用
收藏
页码:539 / 543
页数:5
相关论文
共 34 条
[1]
Ayano E, 2001, ANAL SCI, V17, pi873
[2]
TEMPERATURE-DEPENDENCE OF SWELLING OF CROSS-LINKED POLY(N,N'-ALKYL SUBSTITUTED ACRYLAMIDES) IN WATER [J].
BAE, YH ;
OKANO, T ;
KIM, SW .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1990, 28 (06) :923-936
[3]
Design strategies and performance of custom DNA sequencing primers [J].
Buck, GA ;
Fox, JW ;
Gunthorpe, M ;
Hager, KM ;
Naeve, CW ;
Pon, RT ;
Adams, PS ;
Rush, J .
BIOTECHNIQUES, 1999, 27 (03) :528-+
[4]
Site-specific polymer-streptavidin bioconjugate for pH-controlled binding and triggered release of biotin [J].
Bulmus, V ;
Ding, ZL ;
Long, CJ ;
Stayton, PS ;
Hoffman, AS .
BIOCONJUGATE CHEMISTRY, 2000, 11 (01) :78-83
[5]
DETECTING DNA-DAMAGE [J].
CADET, J ;
WEINFELD, M .
ANALYTICAL CHEMISTRY, 1993, 65 (15) :A675-A682
[6]
MUTUAL INFLUENCE OF PH AND TEMPERATURE ON THE SWELLING OF IONIZABLE AND THERMOSENSITIVE HYDROGELS [J].
FEIL, H ;
BAE, YH ;
FEIJEN, J ;
KIM, SW .
MACROMOLECULES, 1992, 25 (20) :5528-5530
[7]
Ion-pair reversed-phase high-performance liquid chromatography analysis of oligonucleotides: Retention prediction [J].
Gilar, M ;
Fountain, KJ ;
Budman, Y ;
Neue, UD ;
Yardley, KR ;
Rainville, PD ;
Russell, RJ ;
Gebler, JC .
JOURNAL OF CHROMATOGRAPHY A, 2002, 958 (1-2) :167-182
[8]
Purification of crude DNA oligonucleotides by solid-phase extraction and reversed-phase high-performance liquid chromatography [J].
Gilar, M ;
Bouvier, ESP .
JOURNAL OF CHROMATOGRAPHY A, 2000, 890 (01) :167-177
[9]
Heskins M., 1968, J MACROMOL SCI CHEM, V2, P1441, DOI DOI 10.1080/10601326808051910
[10]
CONVENIENT PURIFICATION OF TRITYLATED AND DETRITYLATED OLIGONUCLEOTIDES UP TO 100-MER [J].
HILL, TL ;
MAYHEW, JW .
JOURNAL OF CHROMATOGRAPHY, 1990, 512 :415-431