Mapping the in vivo fitness landscape of a tethered ribosome

被引:1
|
作者
Radford, Felix [1 ,2 ]
Rinehart, Jesse [2 ,3 ]
Isaacs, Farren J. [1 ,2 ,4 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Syst Biol Inst, West Haven, CT 06516 USA
[3] Yale Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
[4] Yale Univ, Dept Biomed Engn, New Haven, CT 06520 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PEPTIDE-BOND FORMATION; ESCHERICHIA-COLI; TRANSFER-RNA; PROTEIN-SYNTHESIS; MEDIATED INCORPORATION; CONSERVED NUCLEOTIDES; STRUCTURAL BASIS; ACTIVE-SITE; AMINO ACIDS; MUTATIONS;
D O I
10.1126/sciadv.ade8934
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fitness landscapes are models of the sequence space of a genetic element that map how each sequence corre-sponds to its activity and can be used to guide laboratory evolution. The ribosome is a macromolecular machine that is essential for protein synthesis in all organisms. Because of the prevalence of dominant lethal mutations, a comprehensive fitness landscape of the ribosomal peptidyl transfer center (PTC) has not yet been attained. Here, we develop a method to functionally map an orthogonal tethered ribosome (oRiboT), which permits com-plete mutagenesis of nucleotides located in the PTC and the resulting epistatic interactions. We found that most nucleotides studied showed flexibility to mutation, and identified epistatic interactions between them, which compensate for deleterious mutations. This work provides a basis for a deeper understanding of ribosome func-tion and malleability and could be used to inform design of engineered ribosomes with applications to synthe-size next-generation biomaterials and therapeutics.
引用
收藏
页数:14
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