FACILE PREPARATION OF 3'-OLIGONUCLEOTIDE-PEPTIDE CONJUGATES
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JUBY, CD
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NATL RES COUNCIL CANADA,BIOTECHNOL RES INST,GENET ENGN SECT,MONTREAL H4P 2R2,QUEBEC,CANADANATL RES COUNCIL CANADA,BIOTECHNOL RES INST,GENET ENGN SECT,MONTREAL H4P 2R2,QUEBEC,CANADA
JUBY, CD
[1
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RICHARDSON, CD
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NATL RES COUNCIL CANADA,BIOTECHNOL RES INST,GENET ENGN SECT,MONTREAL H4P 2R2,QUEBEC,CANADANATL RES COUNCIL CANADA,BIOTECHNOL RES INST,GENET ENGN SECT,MONTREAL H4P 2R2,QUEBEC,CANADA
RICHARDSON, CD
[1
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BROUSSEAU, R
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NATL RES COUNCIL CANADA,BIOTECHNOL RES INST,GENET ENGN SECT,MONTREAL H4P 2R2,QUEBEC,CANADANATL RES COUNCIL CANADA,BIOTECHNOL RES INST,GENET ENGN SECT,MONTREAL H4P 2R2,QUEBEC,CANADA
BROUSSEAU, R
[1
]
机构:
[1] NATL RES COUNCIL CANADA,BIOTECHNOL RES INST,GENET ENGN SECT,MONTREAL H4P 2R2,QUEBEC,CANADA
The solid phase synthesis of 3' deoxyoligonucleotide (17 mer)-peptide conjugates is described. The oligonucleotide is complementary to the template strand of the measles virus in the region of the nucleocapsid protein on the 60 nucleotide leader RNA. The conjugates were synthesized on teflon support using a combination of solid phase FMOC peptide chemistry and phosphoramidite chemistry linked by a branched modifier.