Rare codon recoding for efficient noncanonical amino acid incorporation in mammalian cells

Author:

Ding Wenlong12ORCID,Yu Wei12ORCID,Chen Yulin12ORCID,Lao Lihui1,Fang Yu1ORCID,Fang Chengzhu1,Zhao Hongxia1ORCID,Yang Bo3,Lin Shixian1245ORCID

Affiliation:

1. Life Sciences Institute, The Second Affiliated Hospital of Zhejiang University School of Medicine, Zhejiang Provincial Key Laboratory for Cancer Molecular Cell Biology, Zhejiang University, Hangzhou, China.

2. Center for Life Sciences, Shaoxing Institute, Zhejiang University, Shaoxing, China.

3. Institute of Pharmacology & Toxicology, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

4. Department of Medical Oncology, State Key Laboratory of Transvascular Implantation Devices, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

5. Cancer Center, Zhejiang University, Hangzhou, China.

Abstract

The ability to genetically encode noncanonical amino acids (ncAAs) has empowered proteins with improved or previously unknown properties. However, existing strategies in mammalian cells rely on the introduction of a blank codon to incorporate ncAAs, which is inefficient and limits their widespread applications. In this study, we developed a rare codon recoding strategy that takes advantage of the relative rarity of the TCG codon to achieve highly selective and efficient ncAA incorporation through systematic engineering and big data–model predictions. We highlight the broad utility of this strategy for the incorporation of dozens of ncAAs into various functional proteins at the wild-type protein expression levels, as well as the synthesis of proteins with up to six-site ncAAs or four distinct ncAAs in mammalian cells for downstream applications.

Publisher

American Association for the Advancement of Science (AAAS)

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