Difference between revisions of "Team:Bielefeld-CeBiTec/Description"

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<h2> Expanding the Genetic Code </h2>
 
<h2> Expanding the Genetic Code </h2>
<h4> Abstract </h4>
 
 
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We are exploring the application of unnatural base pairs (UBPs) as an expansion of the genetic code. To prevent loss of the unnatural base pair during reproduction we will utilize several systems including CRISPR/Cas9. The extended genetic code allows the ribosomal incorporation of several non-canonical amino acids (ncAAs) into peptides. With their broad chemical and functional diversity ncAAs provide a variety of promising applications including protein labeling, photocaging, structure analysis and specific protein interactions. Therefore, the development of a new toolkit for the translational incorporation of ncAAs in E. coli would be a great contribu-tion to the iGEM community. The site-specific incorporation of ncAAs requires the directed evolution of tRNA/aminoacyl-tRNA synthetase pairs, which in turn mediate the introduction of an ncAA for a certain codon. This approach enables an optimal orthogonality to the autologous translation apparatus and a high flexibility concern-ing the incorporation of multiple ncAAs. As examples for the successful incorporation of non-canonical amino acids, we will develop a rapid test for prions and a new chromatography method for a mild elution of proteins.
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We are exploring the application of unnatural base pairs as an expansion of the genetic code. To prevent loss of unnatural base pairs during replication, we will utilize several systems including CRISPR/Cas9. The expanded genetic code allows for the ribosomal incorporation of multiple non-canonical amino acids (ncAAs) into peptides. With their broad chemical and functional diversity, ncAAs provide a variety of promising applications including protein labeling, photocaging, structure analysis, and specific protein interactions. Therefore, our innovative toolkit for the translational incorporation of ncAAs in E. coli is a valuable contribution to iGEM. Directed evolution of tRNA/aminoacyl-tRNA synthetase pairs enables the site-specific incorporation of ncAAs into peptides. This approach results in an optimal orthogonality to the autologous translation apparatus and a high flexibility concerning the incorporation of multiple ncAAs. As proof of concept, we are developing a rapid test for prions and a new chromatography method for mild protein elution.  
 
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<p>For more information visit our <b><a href="https://www.researchgate.net/publication/318084694_Expansion_of_the_genetic_code_for_the_translational_incorporation_of_non-canonical_amino_acids">project poster</a></b> on reasearch gate</p>
 
<p>For more information visit our <b><a href="https://www.researchgate.net/publication/318084694_Expansion_of_the_genetic_code_for_the_translational_incorporation_of_non-canonical_amino_acids">project poster</a></b> on reasearch gate</p>

Revision as of 17:04, 23 August 2017

Expanding the Genetic Code

We are exploring the application of unnatural base pairs as an expansion of the genetic code. To prevent loss of unnatural base pairs during replication, we will utilize several systems including CRISPR/Cas9. The expanded genetic code allows for the ribosomal incorporation of multiple non-canonical amino acids (ncAAs) into peptides. With their broad chemical and functional diversity, ncAAs provide a variety of promising applications including protein labeling, photocaging, structure analysis, and specific protein interactions. Therefore, our innovative toolkit for the translational incorporation of ncAAs in E. coli is a valuable contribution to iGEM. Directed evolution of tRNA/aminoacyl-tRNA synthetase pairs enables the site-specific incorporation of ncAAs into peptides. This approach results in an optimal orthogonality to the autologous translation apparatus and a high flexibility concerning the incorporation of multiple ncAAs. As proof of concept, we are developing a rapid test for prions and a new chromatography method for mild protein elution.

For more information visit our project poster on reasearch gate