4.7 Article

Flexizymes for genetic code reprogramming

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NATURE PROTOCOLS
卷 6, 期 6, 页码 779-790

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2011.331

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资金

  1. Japan Society for the Promotion of Science [16101007, 22750145, 22710210]
  2. Industrial Science and Technology Program in the New Energy and Industrial Technology Development Organization
  3. Specially Promoted Research [21000005]
  4. MEST
  5. NRF [R31-2008-000-10103-0]
  6. Grants-in-Aid for Scientific Research [16101007, 22750145, 22710210, 21000005] Funding Source: KAKEN
  7. National Research Foundation of Korea [R31-2011-000-10103-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Genetic code reprogramming is a method for the reassignment of arbitrary codons from proteinogenic amino acids to nonproteinogenic ones; thus, specific sequences of nonstandard peptides can be ribosomally expressed according to their mRNA templates. Here we describe a protocol that facilitates genetic code reprogramming using flexizymes integrated with a custom-made in vitro translation apparatus, referred to as the flexible in vitro translation (FIT) system. Flexizymes are flexible tRNA acylation ribozymes that enable the preparation of a diverse array of nonproteinogenic acyl-tRNAs. These acyl-tRNAs read vacant codons created in the FIT system, yielding the desired nonstandard peptides with diverse exotic structures, such as N-methyl amino acids, D-amino acids and physiologically stable macrocyclic scaffolds. The facility of the protocol allows a wide variety of applications in the synthesis of new classes of nonstandard peptides with biological functions. Preparation of flexizymes and tRNA used for genetic code reprogramming, optimization of flexizyme reaction conditions and expression of nonstandard peptides using the FIT system can be completed by one person in similar to 1 week. However, once the flexizymes and tRNAs are in hand and reaction conditions are fixed, synthesis of acyl-tRNAs and peptide expression is generally completed in 1 d, and alteration of a peptide sequence can be achieved by simply changing the corresponding mRNA template.

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