发明名称 Reengineering mRNA primary structure for enhanced protein production
摘要 Described herein are rules to modify natural mRNAs or to engineer synthetic mRNAs to increase their translation efficiencies. These rules describe modifications to mRNA coding and 3′ UTR sequences intended to enhance protein synthesis by: 1) decreasing ribosomal diversion via AUG or non-canonical initiation codons in coding sequences, and/or 2) by evading miRNA-mediated down-regulation by eliminating one or more miRNA binding sites in coding sequences.
申请公布号 US8853179(B2) 申请公布日期 2014.10.07
申请号 US201013203229 申请日期 2010.02.24
申请人 The Scripps Research Institute 发明人 Mauro Vincent P.;Chappell Stephen A.;Zhou Wei;Edelman Gerald M.
分类号 C12N15/11;C12P21/02 主分类号 C12N15/11
代理机构 Cooley LLP 代理人 Elrifi Ivor;Stock Christina K.;Cooley LLP
主权项 1. A method of improving full-length protein expression efficiency comprising: a) providing a polynucleotide comprising: i) a coding sequence for the full-length protein;ii) a primary initiation codon that is upstream of the coding sequence of the full-length protein, said primary initiation codon encoding the first amino acid of the coding sequence of the full-length protein; andiii) one or more secondary initiation codons located within the coding sequence of the full-length protein downstream of the primary initiation codon; and b) mutating the one or more secondary initiation codons located within the coding sequence of the full-length protein downstream of the primary initiation codon, wherein the mutation results in a decrease in initiation of protein synthesis at the one or more secondary initiation codons, thereby increasing expression efficiency of the full-length protein initiated at the primary initiation codon, wherein mutating the one or more secondary initiation codons located within the coding sequence of the full-length protein downstream of the primary initiation codon comprises mutating one or more nucleotides such that the amino acid sequence of the protein remains unaltered.
地址 LaJolla CA US