Open AccessInterferon induction by mismatched analogues of polyinosinic add . polycytidylic acid [(Ix.U)n.(C)nJ
Author(s) -
Erik De Clercq,
Guang-Fu Huang,
Bharat Bhooshan,
G. Ledley,
Paul F. Torrence
Publication year - 1979
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/7.7.2003
Subject(s) - cycloheximide , biology , interferon , microbiology and biotechnology , dactinomycin , stereochemistry , biochemistry , virology , protein biosynthesis , chemistry
Interruption of the (I)n strand of (I)n.(C)n by unpaired bases [(U)] yielded mismatched analogues, (Ix,U)n.(C)n which were still effective as inducers of interferon, provided the I:U ratio (x) was equal or greater than 10. In highly sensitive interferon-induction systems such as primary rabbit kidney cells and human skin fibroblasts superinduced with cycloheximide and actinomycin D, (I10,U)n.(C)n and (I50,U)n.(C)n proved nearly as active as (I)n.(C)n. By virtue of their increased susceptibility to degradation by nucleases, (Ix,U)n.(C)n complexes with 10 less than or equal to x less than or equal to 50 may be expected not to persist as long in biological fluids as (I)n.(C)n, hence to induce fewer side effects.