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Volumn 29, Issue 9, 2001, Pages 1898-1905

Enhancing the catalytic repertoire of nucleic acids. II. Simultaneous incorporation of amino and imidazolyl functionalities by two modified triphosphates during PCR

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYADENOSINE TRIPHOSPHATE; DNA; NUCLEIC ACID; RESTRICTION ENDONUCLEASE; RIBOZYME; TAQ POLYMERASE; THYMIDINE TRIPHOSPHATE; 2' DEOXYTUBERCIDIN; 2'-DEOXYTUBERCIDIN; DEOXYRIBOZYME; DEOXYURIDINE; DRUG DERIVATIVE; IMIDAZOLE DERIVATIVE; POLYPHOSPHATE; TUBERCIDIN;

EID: 0035339584     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/29.9.1898     Document Type: Article
Times cited : (106)

References (32)
  • 1
    • 0028983570 scopus 로고
    • 2+-dependent RNA phosphoesterase activity
    • 2+-dependent RNA phosphoesterase activity. Chem. Biol., 2, 655-660.
    • (1995) Chem. Biol. , vol.2 , pp. 655-660
    • Breaker, R.R.1    Joyce, G.F.2
  • 2
    • 0029037713 scopus 로고
    • A DNA metalloenzyme with DNA-ligase aclivity
    • Cuenoud, B. and Szostak, J.W. (1995) A DNA metalloenzyme with DNA-ligase aclivity. Nature, 375, 611-614.
    • (1995) Nature , vol.375 , pp. 611-614
    • Cuenoud, B.1    Szostak, J.W.2
  • 3
    • 0028124128 scopus 로고
    • In-vitro evolution of new ribozymes with polynucleotide kinase-activity
    • Lorsch, J.R. and Szostak, J.W. (1994) In-vitro evolution of new ribozymes with polynucleotide kinase-activity. Nature, 371, 31-36.
    • (1994) Nature , vol.371 , pp. 31-36
    • Lorsch, J.R.1    Szostak, J.W.2
  • 4
    • 0030898510 scopus 로고    scopus 로고
    • A general purpose RNA-cleaving DNA enzyme
    • Santoro, S.W. and Joyce, G.F. (1997) A general purpose RNA-cleaving DNA enzyme. Proc. Natl Acad. Sci. USA, 94, 4262-4266.
    • (1997) Proc. Natl Acad. Sci. USA , vol.94 , pp. 4262-4266
    • Santoro, S.W.1    Joyce, G.F.2
  • 7
    • 0030688863 scopus 로고    scopus 로고
    • Peptide bond formation by in vitro selected ribozymes
    • Zhang, B.L. and Cech, T.R. (1997) Peptide bond formation by in vitro selected ribozymes. Nature, 390, 96-100.
    • (1997) Nature , vol.390 , pp. 96-100
    • Zhang, B.L.1    Cech, T.R.2
  • 9
    • 0029956108 scopus 로고    scopus 로고
    • Ribozyme-catalysed amino-acid transfer reactions
    • Lohse, P.A. and Szostak, J.W. (1996) Ribozyme-catalysed amino-acid transfer reactions. Nature, 381, 442-444.
    • (1996) Nature , vol.381 , pp. 442-444
    • Lohse, P.A.1    Szostak, J.W.2
  • 10
    • 0030963855 scopus 로고    scopus 로고
    • RNA-catalysed carbon-carbon bond formation
    • Tarasow, T.M., Tarasow, S.L. and Eaton, B.E. (1997) RNA-catalysed carbon-carbon bond formation. Nature, 389, 54-57.
    • (1997) Nature , vol.389 , pp. 54-57
    • Tarasow, T.M.1    Tarasow, S.L.2    Eaton, B.E.3
  • 12
    • 0029962713 scopus 로고    scopus 로고
    • RNA world: Functional diversity in a nucleoside by carboxyamidation of uridine
    • Dewey, T.M., Zyzniewski, M.C. and Eaton, B.E. (1996) RNA world: functional diversity in a nucleoside by carboxyamidation of uridine. Nucl. Nucl., 15, 1611-1617.
    • (1996) Nucl. Nucl. , vol.15 , pp. 1611-1617
    • Dewey, T.M.1    Zyzniewski, M.C.2    Eaton, B.E.3
  • 13
    • 0029161984 scopus 로고
    • New uridine derivatives for systematic evolution of RNA ligands by exponential enrichment
    • Dewey, T.M., Mundt, A.A., Crouch, G.J., Zyzniewski, M.C. and Eaton, B.E. (1995) New uridine derivatives for systematic evolution of RNA ligands by exponential enrichment. J. Am. Chem. Soc., 117, 8474-8475.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8474-8475
    • Dewey, T.M.1    Mundt, A.A.2    Crouch, G.J.3    Zyzniewski, M.C.4    Eaton, B.E.5
  • 14
    • 0028829020 scopus 로고
    • Palladium catalysis in the synthesis of 8-position modified adenosine, 2′-deoxyadenosine and guanosine
    • Tu, C., Keane, C. and Eaton, B.E. (1995) Palladium catalysis in the synthesis of 8-position modified adenosine, 2′-deoxyadenosine and guanosine. Nucl. Nucl., 14, 1631-1638.
    • (1995) Nucl. Nucl. , vol.14 , pp. 1631-1638
    • Tu, C.1    Keane, C.2    Eaton, B.E.3
  • 15
    • 0034284164 scopus 로고    scopus 로고
    • Expanding the structural and functional diversity of RNA: Analog uridine triphosphates as candidates for in vitro selection of nucleic acids
    • Vaish, N.K., Fraley, A.W., Szostak, J.W. and McLaughlin, L.W. (2000) Expanding the structural and functional diversity of RNA: analog uridine triphosphates as candidates for in vitro selection of nucleic acids. Nucleic Acids Res., 28, 3316-3322.
    • (2000) Nucleic Acids Res. , vol.28 , pp. 3316-3322
    • Vaish, N.K.1    Fraley, A.W.2    Szostak, J.W.3    McLaughlin, L.W.4
  • 17
    • 0032476840 scopus 로고    scopus 로고
    • Expanding the potential of DNA for binding and catalysis: Highly functionalized dUTP derivatives that are substrates for thermostable DNA polymerases
    • Sakthivel, K. and Barbas, C.F. (1998) Expanding the potential of DNA for binding and catalysis: highly functionalized dUTP derivatives that are substrates for thermostable DNA polymerases. Angew. Chem. Int. Ed. Engl. 37, 2872-2875.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 2872-2875
    • Sakthivel, K.1    Barbas, C.F.2
  • 18
    • 0033610480 scopus 로고    scopus 로고
    • Quantitative analysis of receptors for adenosine nucleotides obtained via in vitro selection from a library incorporating a cationic nucleotide analog
    • Battersby, T.R., Ang, D.N., Burgstaller, P., Jurczyk, S.C., Bowser, M.T., Buchanan, D.D., Kennedy, R.T. and Benner, S.A. (1999) Quantitative analysis of receptors for adenosine nucleotides obtained via in vitro selection from a library incorporating a cationic nucleotide analog. J. Am. Chem Soc., 121, 9781-9789.
    • (1999) J. Am. Chem Soc. , vol.121 , pp. 9781-9789
    • Battersby, T.R.1    Ang, D.N.2    Burgstaller, P.3    Jurczyk, S.C.4    Bowser, M.T.5    Buchanan, D.D.6    Kennedy, R.T.7    Benner, S.A.8
  • 19
    • 0032922298 scopus 로고    scopus 로고
    • Expanding the catalytic repertoire of nucleic acid catalysts: Simultaneous incorporation of two modified deoxyribonucleoside triphosphates bearing ammonium and imidazolyl functionalities
    • Perrin, D.M., Garestier, T. and Hélène, C. (1999) Expanding the catalytic repertoire of nucleic acid catalysts: simultaneous incorporation of two modified deoxyribonucleoside triphosphates bearing ammonium and imidazolyl functionalities. Nucl. Nucl., 18, 377-391.
    • (1999) Nucl. Nucl. , vol.18 , pp. 377-391
    • Perrin, D.M.1    Garestier, T.2    Hélène, C.3
  • 20
    • 33845470620 scopus 로고
    • The synthesis of 2′-deoxytubercidin, 2′-deoxyadenosine and related 2′-deoxynucleosides via a novel direct stereospecific sodium salt glycosylation procedure
    • Kazimierczuk, Z., Cottam, H.B., Revankar, G.R. and Robins, R.K. (1984) The synthesis of 2′-deoxytubercidin, 2′-deoxyadenosine and related 2′-deoxynucleosides via a novel direct stereospecific sodium salt glycosylation procedure. J. Am. Chem. Soc., 106, 6379-6382.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 6379-6382
    • Kazimierczuk, Z.1    Cottam, H.B.2    Revankar, G.R.3    Robins, R.K.4
  • 21
    • 0025314762 scopus 로고
    • Synthesis, antiproliferative and antiviral activity of certain 4-substituted and 4,5-disubstituled 7-[(1,3-dihydro-2-propoxy)methyl]pyrrolo[2,3-d]pyrimidines. J
    • Pudlo, J.S., Nassiri, M.R., Kern, E.R., Wotring, L.L., Drach, J.C. and Townsend, L.B. (1990) Synthesis, antiproliferative and antiviral activity of certain 4-substituted and 4,5-disubstituled 7-[(1,3-dihydro-2-propoxy)methyl]pyrrolo[2,3-d]pyrimidines. J. Med. Chem., 33, 1984-1992.
    • (1990) Med. Chem. , vol.33 , pp. 1984-1992
    • Pudlo, J.S.1    Nassiri, M.R.2    Kern, E.R.3    Wotring, L.L.4    Drach, J.C.5    Townsend, L.B.6
  • 22
    • 84981759555 scopus 로고
    • α-Thymidin
    • Hoffer, M. (1960) α-Thymidin. Chem. Ber., 93, 2777-2780.
    • (1960) Chem. Ber. , vol.93 , pp. 2777-2780
    • Hoffer, M.1
  • 23
    • 0030035948 scopus 로고    scopus 로고
    • Oligonucleotides containing C7 propyne analogs of 7-deaza-2′-deoxyguanosine and 7-deaza-2′-deoxyadenosine
    • Buhr, C.A., Wagner, R.W., Grant, E. and Froehler, B.C (1996) Oligonucleotides containing C7 propyne analogs of 7-deaza-2′-deoxyguanosine and 7-deaza-2′-deoxyadenosine. Nucleic Acids Res., 24, 2974-2980.
    • (1996) Nucleic Acids Res. , vol.24 , pp. 2974-2980
    • Buhr, C.A.1    Wagner, R.W.2    Grant, E.3    Froehler, B.C.4
  • 24
    • 0029844007 scopus 로고    scopus 로고
    • Palladium-catalysed cross coupling of 7-iodo-2′-deoxytubercidin with terminal alkynes
    • Seela, F. and Zulauf, M. (1996) Palladium-catalysed cross coupling of 7-iodo-2′-deoxytubercidin with terminal alkynes. Synthesis, 726-730.
    • (1996) Synthesis , pp. 726-730
    • Seela, F.1    Zulauf, M.2
  • 25
    • 0008519637 scopus 로고    scopus 로고
    • The DNA-stablising nucleoside 7-iodo-2′-deoxytubercidin: Its structure in the solid state and in solution
    • Seela, F., Zulauf, M., Rosemeyer, H. and Reuter, H. (1996) The DNA-stablising nucleoside 7-iodo-2′-deoxytubercidin: its structure in the solid state and in solution. J. Chem. Soc. Perkin Trans. II. 2373-2376.
    • (1996) J. Chem. Soc. Perkin Trans. II. , pp. 2373-2376
    • Seela, F.1    Zulauf, M.2    Rosemeyer, H.3    Reuter, H.4
  • 26
    • 0032720771 scopus 로고    scopus 로고
    • Oligonucleotides containing 7-deazaadenines: The influence of the 7-substituent chain length and charge on the duplex stability
    • Seela, F. and Zulauf, M. (1999) Oligonucleotides containing 7-deazaadenines: the influence of the 7-substituent chain length and charge on the duplex stability. Helv. Chim. Acta. 82, 1878-1898.
    • (1999) Helv. Chim. Acta , vol.82 , pp. 1878-1898
    • Seela, F.1    Zulauf, M.2
  • 27
    • 0029102264 scopus 로고
    • Duplex stabilisation of DNA: Oligonucleotides containing 7-substituted 7-deazaadenines
    • Seela, F. and Thomas, H. (1995) Duplex stabilisation of DNA: oligonucleotides containing 7-substituted 7-deazaadenines. Helv. Chim. Acta, 78, 94-108.
    • (1995) Helv. Chim. Acta , vol.78 , pp. 94-108
    • Seela, F.1    Thomas, H.2
  • 28
    • 0023643409 scopus 로고
    • Poly(2-amino-8-methyldeoxyadenylinic acid) - Contrasting effects in deoxynucleotides and ribopolynucleotides of 2-amino and 8-methyl substituents
    • Kanaya, E., Howard, F.B., Frazier, J. and Miles, H.T. (1987) Poly(2-amino-8-methyldeoxyadenylinic acid) - contrasting effects in deoxynucleotides and ribopolynucleotides of 2-amino and 8-methyl substituents. Biochemistry, 26, 7159-7165.
    • (1987) Biochemistry , vol.26 , pp. 7159-7165
    • Kanaya, E.1    Howard, F.B.2    Frazier, J.3    Miles, H.T.4
  • 29
    • 20444449794 scopus 로고    scopus 로고
    • Oligonucleotides containing 7-or 8-methyl-7-deazaguanine:Steric requirements of major groove substituents on the DNA structure
    • Seela, F. and Chen, Y.M. (1996) Oligonucleotides containing 7-or 8-methyl-7-deazaguanine:steric requirements of major groove substituents on the DNA structure. J. Chem. Soc. Chem. Commun., 2263-2264.
    • (1996) J. Chem. Soc. Chem. Commun. , pp. 2263-2264
    • Seela, F.1    Chen, Y.M.2
  • 31
    • 0034620188 scopus 로고    scopus 로고
    • Novel syntheses of (Z)-alkene and alkane base-modified nucleosides
    • Lee, S.E., Vyle, J.S., Williams, D.M. and Grasby, J.A. (2000) Novel syntheses of (Z)-alkene and alkane base-modified nucleosides. Tetrahedron Lett., 41, 267-270.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 267-270
    • Lee, S.E.1    Vyle, J.S.2    Williams, D.M.3    Grasby, J.A.4
  • 32
    • 0023748537 scopus 로고
    • Simple synthesis of 5-vinyl-and 5-ethynyl-2′-deoxyuridine-5′-triphosphates
    • Kovacz, T. and Ötvös, L. (1988) Simple synthesis of 5-vinyl-and 5-ethynyl-2′-deoxyuridine-5′-triphosphates. Tetrahedron Lett., 29, 4525-4528.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 4525-4528
    • Kovacz, T.1    Ötvös, L.2


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