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Volumn 18, Issue 3, 2008, Pages 245-255

An efficient biodelivery system for antisense polyamide nucleic acid (PNA)

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMIC ACID; DISULFIDE; GLUTATHIONE; PEPTIDE NUCLEIC ACID; PHOSPHONIUM DERIVATIVE; TRIPHENYLPHOSPHONIUM; UNCLASSIFIED DRUG;

EID: 51849110440     PISSN: 15454576     EISSN: None     Source Type: Journal    
DOI: 10.1089/oli.2008.0126     Document Type: Article
Times cited : (16)

References (26)
  • 2
    • 0032084927 scopus 로고    scopus 로고
    • Solid-phase synthesis of peptide nucleic acid (PNA) monomers and their oligomerization using disulphide anchoring linkers
    • ALDRIAN-HERRADA, G., RABIE, A., WINTERSTEIGER, R., and BRUGIDOU, J. (1998). Solid-phase synthesis of peptide nucleic acid (PNA) monomers and their oligomerization using disulphide anchoring linkers. J. Peptide Sci. 4, 266-281.
    • (1998) J. Peptide Sci , vol.4 , pp. 266-281
    • ALDRIAN-HERRADA, G.1    RABIE, A.2    WINTERSTEIGER, R.3    BRUGIDOU, J.4
  • 3
    • 0038246490 scopus 로고    scopus 로고
    • Synthesis and properties of ester-linked peptide nucleic acids prodrug conjugates
    • BENDIFALLAH, N., KRISTENSEN, E., DAHL, O., KOPPELHUS, U., and NIELSEN, P.E. (2003) Synthesis and properties of ester-linked peptide nucleic acids prodrug conjugates. Bioconjugate Chem. 14, 588-592.
    • (2003) Bioconjugate Chem , vol.14 , pp. 588-592
    • BENDIFALLAH, N.1    KRISTENSEN, E.2    DAHL, O.3    KOPPELHUS, U.4    NIELSEN, P.E.5
  • 4
    • 33646950391 scopus 로고    scopus 로고
    • Evaluation of cel-lpenetrating peptides (CPPs) as vehicles for intracellular delivery of antisense peptide nucleic acid (PNA)
    • BENDIFALLAH, N., RASMUSSEN, F.W., ZACHAR, W., EBBESEN, P., NIELSEN, P.E., and KOPPELHUS, U. (2006). Evaluation of cel-lpenetrating peptides (CPPs) as vehicles for intracellular delivery of antisense peptide nucleic acid (PNA). Bioconjugate Chem. 17, 750-758.
    • (2006) Bioconjugate Chem , vol.17 , pp. 750-758
    • BENDIFALLAH, N.1    RASMUSSEN, F.W.2    ZACHAR, W.3    EBBESEN, P.4    NIELSEN, P.E.5    KOPPELHUS, U.6
  • 5
    • 0030997133 scopus 로고    scopus 로고
    • Chemical barriers to human immunodeficiency virus type 1 (HIV-1) infection: Retrovirucidal activity of UC781, a thiocarboxanilide nonnucleoside inhibitor of HIV-1 reverse transcriptase
    • BORKOW, G., BARNARD, J., NGUYEN, T.M., BELMONTE, A., WAINBERG, M.A., and PARNIAK, M.A. (1997). Chemical barriers to human immunodeficiency virus type 1 (HIV-1) infection: retrovirucidal activity of UC781, a thiocarboxanilide nonnucleoside inhibitor of HIV-1 reverse transcriptase. J. Virol. 71, 3023-3030.
    • (1997) J. Virol , vol.71 , pp. 3023-3030
    • BORKOW, G.1    BARNARD, J.2    NGUYEN, T.M.3    BELMONTE, A.4    WAINBERG, M.A.5    PARNIAK, M.A.6
  • 6
    • 34648833981 scopus 로고    scopus 로고
    • Mechanism of RNA cleavage by sequence specific polyamide nucleic acid-neamine conjugate
    • CHAUBEY, B., TRIPATHI, S., DESIRE, .J., BAUSSANE, I., DECOUT, J.L., and PANDEY, V.N. (2007). Mechanism of RNA cleavage by sequence specific polyamide nucleic acid-neamine conjugate. Oligonucleotides 17, 302-313.
    • (2007) Oligonucleotides , vol.17 , pp. 302-313
    • CHAUBEY, B.1    TRIPATHI, S.2    DESIRE, J.3    BAUSSANE, I.4    DECOUT, J.L.5    PANDEY, V.N.6
  • 7
    • 11344260182 scopus 로고    scopus 로고
    • A PNA-transportan conjugate targeted to the TAR region of the HIV-1 genome exhibits both antiviral and virucidal properties
    • CHAUBEY, B., TRIPATHI, S., GANGULY, S., HARRIS, D., CASALE, R. A., and PANDEY, V. N. (2005). A PNA-transportan conjugate targeted to the TAR region of the HIV-1 genome exhibits both antiviral and virucidal properties. Virology 331, 418-428.
    • (2005) Virology , vol.331 , pp. 418-428
    • CHAUBEY, B.1    TRIPATHI, S.2    GANGULY, S.3    HARRIS, D.4    CASALE, R.A.5    PANDEY, V.N.6
  • 9
    • 0016379917 scopus 로고
    • Relationships between inhibition constants and fractional inhibitions in enzyme-catalysed reactions with different numbers of reactants, different reaction mechanisms, and different types of mechanisms of inhibition
    • CHOU, T.-C. (1974). Relationships between inhibition constants and fractional inhibitions in enzyme-catalysed reactions with different numbers of reactants, different reaction mechanisms, and different types of mechanisms of inhibition. Mol. Pharm. 39, 235-247.
    • (1974) Mol. Pharm , vol.39 , pp. 235-247
    • CHOU, T.-C.1
  • 10
    • 51849167348 scopus 로고
    • Derivation and properties of Michaelis-Menten type and hill equations for reference ligands
    • CHOU, T.-C. (1977). Derivation and properties of Michaelis-Menten type and hill equations for reference ligands. J. Theoret. Biol. 272, 16010-16017.
    • (1977) J. Theoret. Biol , vol.272 , pp. 16010-16017
    • CHOU, T.-C.1
  • 11
    • 51849152478 scopus 로고    scopus 로고
    • Improved synthons for the synthesis and deprotection of peptide nucleic acids under mild conditions
    • PCT Int. Appl. WO 96/40685
    • COULL, J.M., EGHOLM, M., HODGE, R.P., ISMAIL, M., and RAJUR, S.B. (1996). Improved synthons for the synthesis and deprotection of peptide nucleic acids under mild conditions. PCT Int. Appl. WO 96/40685.
    • (1996)
    • COULL, J.M.1    EGHOLM, M.2    HODGE, R.P.3    ISMAIL, M.4    RAJUR, S.B.5
  • 12
    • 0346725016 scopus 로고    scopus 로고
    • Delivery of antisense peptide nucleic acids (PNAs) to the cytosol by disulphide conjugation to a lipophilic cation
    • FILIPOVSKA, A., ECCLES, M.R., SMITH, R.A., and MURPHY, M.P. (2004) Delivery of antisense peptide nucleic acids (PNAs) to the cytosol by disulphide conjugation to a lipophilic cation. FEBS Lett. 556, 180-186.
    • (2004) FEBS Lett , vol.556 , pp. 180-186
    • FILIPOVSKA, A.1    ECCLES, M.R.2    SMITH, R.A.3    MURPHY, M.P.4
  • 13
    • 33646716870 scopus 로고    scopus 로고
    • Releasable luciferin-transporter conjugates: Tools for the real-time analysis of cellular uptake and release
    • JONES, L.R., GOUN, E.A., SHINDE, R., ROTHBARD, J.B., CONTAG, C.H., and WENDER, P.A. (2006). Releasable luciferin-transporter conjugates: tools for the real-time analysis of cellular uptake and release. J. Am. Chem. Soc. 128, 6526-6527.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 6526-6527
    • JONES, L.R.1    GOUN, E.A.2    SHINDE, R.3    ROTHBARD, J.B.4    CONTAG, C.H.5    WENDER, P.A.6
  • 14
    • 0037428953 scopus 로고    scopus 로고
    • Cellular delivery of peptide nucleic acid (PNA)
    • KOPPELHUS, U., and NIELSEN, P.E. (2003). Cellular delivery of peptide nucleic acid (PNA). Adv. Drug Deliver. Rev. 55, 267-280.
    • (2003) Adv. Drug Deliver. Rev , vol.55 , pp. 267-280
    • KOPPELHUS, U.1    NIELSEN, P.E.2
  • 16
    • 0028819889 scopus 로고
    • Mononucleoside phosphotriester d erivatives w ith S-acyl-2-thioethyl bioreversible phosphate-protecting groups: Intracellular delivery of 3′-azido-2′, 3′-dideoxythymidine 5′-monophosphate
    • LEFEBVRE, I., PÉRIGAUD, C., POMPON, A., AUBERTIN, A.-M., GIRARDET, J.-L., KIM, A., GOSSELIN, G., and IMBACH, J.-L. (1995). Mononucleoside phosphotriester d erivatives w ith S-acyl-2-thioethyl bioreversible phosphate-protecting groups: intracellular delivery of 3′-azido-2′, 3′-dideoxythymidine 5′-monophosphate. J. Med. Chem. 38, 3941-3950.
    • (1995) J. Med. Chem , vol.38 , pp. 3941-3950
    • LEFEBVRE, I.1    PÉRIGAUD, C.2    POMPON, A.3    AUBERTIN, A.-M.4    GIRARDET, J.-L.5    KIM, A.6    GOSSELIN, G.7    IMBACH, J.-L.8
  • 17
    • 0031193332 scopus 로고    scopus 로고
    • Fluorescein-conjugated lysine monomers for solid phase synthesis of fluorescent peptides and PNA oligomers
    • LOHSE, J., NIELSEN, P.E., HARRIT, N., and DAHL, O. (1997). Fluorescein-conjugated lysine monomers for solid phase synthesis of fluorescent peptides and PNA oligomers. Bioconjugate Chem. 8, 503-509.
    • (1997) Bioconjugate Chem , vol.8 , pp. 503-509
    • LOHSE, J.1    NIELSEN, P.E.2    HARRIT, N.3    DAHL, O.4
  • 18
    • 34250800263 scopus 로고    scopus 로고
    • A "Ready-To-Use" fluorescent-labelled-cysteine-TBTP (4-thiobutyltriphenylphosphonium) synthon to investigate the delivery of non-permeable PNA (Peptide Nucleic Acids)-based compounds to cells
    • MEHIRI, M., CALDARELLI, S., DI GIORGIO, A., BAROUILLET, T., DOGLIO, A., CONDOM, R., and PATINO, N. (2007). A "Ready-To-Use" fluorescent-labelled-cysteine-TBTP (4-thiobutyltriphenylphosphonium) synthon to investigate the delivery of non-permeable PNA (Peptide Nucleic Acids)-based compounds to cells. Bioorganic Chem. 35, 313-326.
    • (2007) Bioorganic Chem , vol.35 , pp. 313-326
    • MEHIRI, M.1    CALDARELLI, S.2    DI GIORGIO, A.3    BAROUILLET, T.4    DOGLIO, A.5    CONDOM, R.6    PATINO, N.7
  • 19
    • 0028998273 scopus 로고    scopus 로고
    • MELTZER, P.C., LIANG, A.Y., and MATSUDAIRA, P. (1995). Peptide nucleic acids: synthesis of thymine, adenine, guanine, and cytosine nucleobases. J. Org. Chem. 60, 4305-4308.
    • MELTZER, P.C., LIANG, A.Y., and MATSUDAIRA, P. (1995). Peptide nucleic acids: synthesis of thymine, adenine, guanine, and cytosine nucleobases. J. Org. Chem. 60, 4305-4308.
  • 20
    • 0035339611 scopus 로고    scopus 로고
    • Targeting peptide nucleic acid (PNA) oligomers to mitochondria within cells by conjugation to lipophilic cations: Implications for mitochondrial DNA replication, expression and disease
    • MURATOVSKA, A., LIGHTOWLERS, R.N., TAYLOR, R.W., TURNBULL, D.M., SMITH, R.A.J., WILCE, J.A., MARTIN, S.W., and MURPHY, M.P. (2001). Targeting peptide nucleic acid (PNA) oligomers to mitochondria within cells by conjugation to lipophilic cations: implications for mitochondrial DNA replication, expression and disease. Nucleic Acids Res. 29, 1852-1863.
    • (2001) Nucleic Acids Res , vol.29 , pp. 1852-1863
    • MURATOVSKA, A.1    LIGHTOWLERS, R.N.2    TAYLOR, R.W.3    TURNBULL, D.M.4    SMITH, R.A.J.5    WILCE, J.A.6    MARTIN, S.W.7    MURPHY, M.P.8
  • 24
    • 23844510658 scopus 로고    scopus 로고
    • Anti-HIV-1 activity of anti-TAR polyamide nucleic acid conjugated with various membrane transducing peptides
    • TRIPATHI, S., CHAUBEY, B., GANGULY, S., HARRIS, D., CASALE, R.A., and PANDEY, V.N. (2005). Anti-HIV-1 activity of anti-TAR polyamide nucleic acid conjugated with various membrane transducing peptides. Nucleic Acids Res. 33, 4345-4356.
    • (2005) Nucleic Acids Res , vol.33 , pp. 4345-4356
    • TRIPATHI, S.1    CHAUBEY, B.2    GANGULY, S.3    HARRIS, D.4    CASALE, R.A.5    PANDEY, V.N.6
  • 25
    • 34247606647 scopus 로고    scopus 로고
    • Anti HIV-1 virucidal activity of polyamide nucleic acid-membrane transducing peptide conjugates targeted to primer binding site of HIV-1 genome
    • TRIPATHI, S., CHAUBEY, B., BARTON, B.E., and PANDEY, V.N. (2007). Anti HIV-1 virucidal activity of polyamide nucleic acid-membrane transducing peptide conjugates targeted to primer binding site of HIV-1 genome. Virology 20, 91-103.
    • (2007) Virology , vol.20 , pp. 91-103
    • TRIPATHI, S.1    CHAUBEY, B.2    BARTON, B.E.3    PANDEY, V.N.4
  • 26
    • 33845575774 scopus 로고    scopus 로고
    • Structural requirements for cellular uptake and antisense activity of peptide nucleic acids conjugated with various peptides
    • WOLF, Y., PRITZ, S., ABES, S., BIENERT, M., LEBLEU, B., and OEHLKE, J. (2006). Structural requirements for cellular uptake and antisense activity of peptide nucleic acids conjugated with various peptides. Biochemistry 45, 14944-14954.
    • (2006) Biochemistry , vol.45 , pp. 14944-14954
    • WOLF, Y.1    PRITZ, S.2    ABES, S.3    BIENERT, M.4    LEBLEU, B.5    OEHLKE, J.6


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