Abstract
The naturally occurring RNA-nucleopeptide H-Ala-Tyr[5'-pUUAAAAC-3']-NH2 is prepared via a solid-phase phosphite triester approach using N-SiOMB/O-TBDMS-protected nucleosides. Preliminary 1H-NMR studies show that the peptidyl unit has a remarkable effect on the conformational behaviour of the RNA moiety in the nucleopeptide.
MeSH terms
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Magnetic Resonance Spectroscopy
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Nucleic Acid Conformation
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Nucleoproteins / chemistry
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Oligoribonucleotides / chemistry*
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Peptide Fragments / chemical synthesis*
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Peptide Fragments / chemistry
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Poliovirus / chemistry*
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RNA, Viral / chemistry*
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Ribonucleoproteins / chemical synthesis*
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Ribonucleoproteins / chemistry
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Viral Proteins / chemical synthesis*
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Viral Proteins / chemistry
Substances
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Nucleoproteins
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Oligoribonucleotides
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Peptide Fragments
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RNA, Viral
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Ribonucleoproteins
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Viral Proteins