A convenient 'on line' solid-phase synthesis of oligonucleotides conjugated at the 3'-end with peptides by means of a polymeric support linking the first nucleoside via the base has been developed. A 17-mer designed for antisense experiments against HIV-1, linking at the 3'-terminus the tripeptide Gly-Gly-His, was prepared in good yields and characterized by MALDI-TOF mass spectrometry.

A new solid-phase synthesis of oligonucleotides 3’-conjugated with peptides / DE NAPOLI, L., A., M., Montesarchio, D., Piccialli, G., E., B., E., B., Rossi, F.. - In: BIOORGANIC & MEDICINAL CHEMISTRY. - ISSN 0968-0896. - ELETTRONICO. - 7:(1999), pp. 395-400. [10.1016/S0968-0896(98)00250-8]

A new solid-phase synthesis of oligonucleotides 3’-conjugated with peptides

DE NAPOLI, LORENZO;MONTESARCHIO, DANIELA;PICCIALLI, GENNARO;ROSSI, FILOMENA
1999

Abstract

A convenient 'on line' solid-phase synthesis of oligonucleotides conjugated at the 3'-end with peptides by means of a polymeric support linking the first nucleoside via the base has been developed. A 17-mer designed for antisense experiments against HIV-1, linking at the 3'-terminus the tripeptide Gly-Gly-His, was prepared in good yields and characterized by MALDI-TOF mass spectrometry.
1999
A new solid-phase synthesis of oligonucleotides 3’-conjugated with peptides / DE NAPOLI, L., A., M., Montesarchio, D., Piccialli, G., E., B., E., B., Rossi, F.. - In: BIOORGANIC & MEDICINAL CHEMISTRY. - ISSN 0968-0896. - ELETTRONICO. - 7:(1999), pp. 395-400. [10.1016/S0968-0896(98)00250-8]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/155387
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