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 PMID:40536028  

Directed Evolution of a SelB Variant that Does Not Require a Selenocysteine Insertion Sequence Element for Function.

Satoshi Ishida | Arno Gundlach | Clayton W Kosonocky | Andrew D Ellington
ACS synthetic biology | 2025

In bacteria, the incorporation of selenocysteine is achieved through the interaction of the selenocysteine specific elongation factor (SelB) with selenocysteine-charged tRNASec and a selenocysteine insertion sequence (SECIS) element adjacent to an opal stop codon in an mRNA. The more generalized, SECIS-independent incorporation of selenocysteine is of interest because of the high nucleophilicity of selenium and the greater durability of diselenide bonds. It is likely that during the course of evolution, selenocysteine insertion originally arose without the presence of a SECIS element, relying only on SelB. Herein, we undertake experiments to evolve an ancestral version of SelB that is SECIS-independent and show that not only can this protein (SelB-v2) generally incorporate selenocysteine across from stop codons but also that the new, orthogonal translation factor can be repurposed to other amino acids, such as serine. Given the delicate energetic balancing act already performed by EF-Tu, this achievement raises the possibility that greatly expanded genetic codes that relied in part on SelB-based loading can now be contrived.

Pubmed ID: 40536028

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University of Texas at Austin Biological Mass Spectrometry Proteomics Core Facility (service resource)

RRID:SCR_021728

Proteomics and Metabolomics services and collaborative efforts are provided at Biological Mass Spectrometry Facility. We use high resolution Orbitrap mass spectrometers with UPLC at high flow for metabolomics and nanoUPLC for proteomics work. We have Bruker Autoflex for self service MALDI. Our proteomics services are protein ID, quantitation, and modification analysis, with fractionation for deeper coverage and de novo sequencing of mAbs available. We collaborate for customized projects. We have untargeted metabolomics for quantitative or qualitative analysis of extracted metabolites using C18 column.

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University of Texas at Austin Biological Mass Spectrometry Proteomics Core Facility (service resource)

RRID:SCR_021728

Proteomics and Metabolomics services and collaborative efforts are provided at Biological Mass Spectrometry Facility. We use high resolution Orbitrap mass spectrometers with UPLC at high flow for metabolomics and nanoUPLC for proteomics work. We have Bruker Autoflex for self service MALDI. Our proteomics services are protein ID, quantitation, and modification analysis, with fractionation for deeper coverage and de novo sequencing of mAbs available. We collaborate for customized projects. We have untargeted metabolomics for quantitative or qualitative analysis of extracted metabolites using C18 column.

View all literature mentions