SYNTHESIS OF WELL-DEFINED PHOSPHATE-METHYLATED DNA FRAGMENTS - THE APPLICATION OF POTASSIUM CARBONATE IN METHANOL AS DEPROTECTING REAGENT

被引:51
作者
KUIJPERS, WHA [1 ]
HUSKENS, J [1 ]
KOOLE, LH [1 ]
VANBOECKEL, CAA [1 ]
机构
[1] EINDHOVEN UNIV TECHNOL,DEPT ORGAN CHEM,5600 MB EINDHOVEN,NETHERLANDS
关键词
D O I
10.1093/nar/18.17.5197
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new deprotection procedure in the synthesis of (partially) phosphate-methylated oligodeoxynucleotides has been developed, involving treatment of fully protected DNA fragments with methanolic potassium carbonate. It is shown that base deprotection can be accomplished in potassium carbonate/methanol without aftecting the methyl phosphotriesters. This methodology enables us to synthesize, both in solution and on a solid support, DNA fragments which are phosphate-methylated at defined positions. The solid phase synthesis, however, turns out to be accompanied by considerable demethylation of the phosphotriesters. It is demonstrated that this demethylation does not occur during the deprotection or work-up procedure. Furthermore, it was found that the latter side-reaction is suppressed when the standard capping procedure with acetic anhydride is included. © 1990 Oxford University Press.
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收藏
页码:5197 / 5205
页数:9
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共 33 条
  • [1] AGARWAL S, 1987, TETRAHEDRON LETT, V28, P3539
  • [2] ATKINSON T, 1984, OLIGONUCLEOTIDE SYNT, P35
  • [3] CUBBELIS MV, 1985, J CHROMATOGR, V329, P406
  • [4] NUCLEOSIDE PHOSPHOROTHIOATES
    ECKSTEIN, F
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1985, 54 : 367 - 402
  • [5] ALKYL PHOSPHOTRIESTER MODIFIED OLIGODEOXYRIBONUCLEOTIDES .5. SYNTHESIS AND ABSOLUTE-CONFIGURATION OF RP AND SP DIASTEREOMERS OF AN ETHYL PHOSPHOTRIESTER (ET) MODIFIED ECORI RECOGNITION SEQUENCE, D[GGAA(ET)TTCC] - A SYNTHETIC APPROACH TO REGIOSPECIFIC AND STEREOSPECIFIC ETHYLATION-INTERFERENCE STUDIES
    GALLO, KA
    SHAO, KL
    PHILLIPS, LR
    REGAN, JB
    KOZIOLKIEWICZ, M
    UZNANSKI, B
    STEC, WJ
    ZON, G
    [J]. NUCLEIC ACIDS RESEARCH, 1986, 14 (18) : 7405 - 7420
  • [6] LEVULINIC ESTERS - ALCOHOL PROTECTING GROUP APPLICABLE TO SOME NUCLEOSIDES
    HASSNER, A
    STRAND, G
    RUBINSTEIN, M
    PATCHORNIK, A
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (06) : 1614 - 1615
  • [7] THE 9-FLUORENYLMETHOXYCARBONYL (FMOC) GROUP FOR THE PROTECTION OF AMINO FUNCTIONS OF CYTIDINE, ADENOSINE, GUANOSINE AND THEIR 2'-DEOXYSUGAR DERIVATIVES
    HEIKKILA, J
    CHATTOPADHYAYA, J
    [J]. ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1983, 37 (03): : 263 - 265
  • [8] SYNTHESIS OF DEOXYNUCLEOSIDE METHYLPHOSPHONATES VIA A PHOSPHONAMIDITE APPROACH
    JAGER, A
    ENGELS, J
    [J]. TETRAHEDRON LETTERS, 1984, 25 (14) : 1437 - 1440
  • [9] SYNTHESIS OF PHOSPHATE-METHYLATED DNA FRAGMENTS USING 9-FLUORENYLMETHOXYCARBONYL AS TRANSIENT BASE PROTECTING GROUP
    KOOLE, LH
    MOODY, HM
    BROEDERS, NLHL
    QUAEDFLIEG, PJLM
    KUIJPERS, WHA
    VANGENDEREN, MHP
    COENEN, AJJM
    VANDERWAL, S
    BUCK, HM
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (07) : 1657 - 1664
  • [10] THE 9-FLUORENYLMETHYLOXYCARBONYL GROUP AS A 5'-OH PROTECTION IN OLIGONUCLEOTIDE SYNTHESIS
    MA, YX
    SONVEAUX, E
    [J]. BIOPOLYMERS, 1989, 28 (05) : 965 - 973