发明名称 Antisense oligonucleotide antibiotics complementary to the macromolecular synthesis operon, methods of treating bacterial infections and methods for identification of bacteria
摘要 A method of interrupting the expression of a macromolecular synthesis operon in bacteria comprising the step of binding an antisense oligonucleotide to a single stranded DNA or to a mRNA transcribed from the macromolecular synthesis operon. The antisense oligonucleotide can be either sequence specific to a unique intergenic sequence or a sequence specific to a bacterial homologous sequence. By interrupting the expression of the macromolecular synthesis operon bacterial infections can be treated. Specific antisense oligonucleotides are disclosed. The ability of the antisense oligonucleotide to bind the mRNA or single stranded DNA also allows the identification of the bacteria by using a unique intergenic antisense oligonucleotide to bind to the single stranded DNA or to the mRNA transcribed from the macromolecular synthesis operon. A method for competitively inhibiting the protein products of the MMS operon with oligonucleotides is also disclosed. Methods of identifying unique intergenic sequence is also disclosed.
申请公布号 US5294533(A) 申请公布日期 1994.03.15
申请号 US19900572191 申请日期 1990.08.23
申请人 BAYLOR COLLEGE OF MEDICINE;ABBOTT LABORATORIES 发明人 LUPSKI, JAMES R.;KATZ, LEONARD
分类号 C12N15/09;A61K31/70;A61K38/00;A61P31/04;C07H21/04;C07K14/195;C07K14/285;C12N15/113;C12N15/31;C12Q1/04;C12Q1/18;C12Q1/68;C12R1/125;C12R1/19;C12R1/42;(IPC1-7):C21Q1/68;C12N15/00;C12N15/11 主分类号 C12N15/09
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