Abstract |
A discrete tetravalent conjugate, 7a ( LJP 394), consisting of four oligonucleotides attached to a common carrier or platform was prepared. Single-stranded oligonucleotide 20-mers consisting of alternating deoxycytidine- deoxyadenosine nucleotides, (CA)10, were attached to a tetrabromoacetylated platform by displacement with sulfhydryl-terminated linkers. The tetrabromoacetylated platform 3a was synthesized in three steps using triethylene glycol bis-(chloroformate). The single-stranded conjugate was characterized by polyacrylamide gel electrophoresis, DNA sequencing, phosphate analysis, carbon and nitrogen combustion analysis, and correlation of stoichiometry to conversion in the conjugation process. HPLC and capillary electrophoretic methods were developed to evaluate purity. The tetrakis, single-stranded conjugate was annealed with a stoichiometric amount of a complementary single-stranded oligonucleotide 20-mer consisting of alternating thymidine- deoxyguanosine nucleotides, (TG)10. The double-stranded conjugate LJP 394 was characterized by melt temperature and hyperchromicity, phosphate analysis, and carbon and nitrogen combustion analysis. LJP 394 inhibits binding of DNA to anti-double-stranded oligonucleotide antibodies and reduces anti- oligonucleotide-specific plaque (antibody)-forming cells in an immunized mouse model by a proposed mechanism involving cross-linking B cell surface immunoglobins.
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Authors | D S Jones, P A Barstad, M J Feild, J P Hachmann, M S Hayag, K W Hill, G M Iverson, D A Livingston, M S Palanki, A R Tibbetts |
Journal | Journal of medicinal chemistry
(J Med Chem)
Vol. 38
Issue 12
Pg. 2138-44
(Jun 09 1995)
ISSN: 0022-2623 [Print] United States |
PMID | 7783145
(Publication Type: Journal Article)
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Chemical References |
- Oligonucleotides
- abetimus
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Topics |
- Animals
- Antibody-Producing Cells
(drug effects, immunology)
- Disease Models, Animal
- Female
- Hemolytic Plaque Technique
- Humans
- Lupus Nephritis
(drug therapy, immunology)
- Mice
- Mice, Inbred C57BL
- Oligonucleotides
(antagonists & inhibitors, chemistry, pharmacology, therapeutic use)
- Spleen
(drug effects, immunology, pathology)
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