SYNTHESIS OF OLIGODEOXYNUCLEOTIDES CONTAINING N-4-MERCAPTOETHYLCYTOSINE AND THEIR USE IN THE PREPARATION OF OLIGONUCLEOTIDE-PEPTIDE CONJUGATES CARRYING C-MYC TAG-SEQUENCE

Citation
D. Gottschling et al., SYNTHESIS OF OLIGODEOXYNUCLEOTIDES CONTAINING N-4-MERCAPTOETHYLCYTOSINE AND THEIR USE IN THE PREPARATION OF OLIGONUCLEOTIDE-PEPTIDE CONJUGATES CARRYING C-MYC TAG-SEQUENCE, Bioconjugate chemistry, 9(6), 1998, pp. 831-837
Citations number
25
Categorie Soggetti
Chemistry Inorganic & Nuclear",Biology,"Biochemical Research Methods",Chemistry
Journal title
ISSN journal
10431802
Volume
9
Issue
6
Year of publication
1998
Pages
831 - 837
Database
ISI
SICI code
1043-1802(1998)9:6<831:SOOCN>2.0.ZU;2-5
Abstract
The preparation and properties of oligodeoxynucleotides containing mer captoethyl groups at position N-4 of cytosine are described. The resul ting thiol-oligodeoxynucleotides were reacted with a maleimido-peptide carrying the c-myc tag-sequence. The peptide-oligonucleotide conjugat e is specifically recognized by an anti c-myc monoclonal antibody, thu s constituting a labeling system with sensitivity similar to other exi sting methods of nonradioactive labeling.