<scp>GGAssembler</scp>: Precise and economical design and synthesis of combinatorial mutation libraries

Golden Gate assembly (GGA) can seamlessly generate full-length genes from DNA fragments. In principle, GGA could be used to design combinatorial mutation libraries for protein engineering, but creating accurate, complex, and cost-effective libraries has been challenging. We present GGAssembler, a graph-theoretical method for economical design of DNA fragments that assemble a combinatorial library that encodes any desired diversity. We used GGAssembler for one-pot in vitro assembly of camelid antibody libraries comprising >10<sup>5</sup> variants with DNA costs <0.007$ per variant and dropping significantly with increased library complexity. >93% of the desired variants were present in the assembly product and >99% were represented within the expected order of magnitude as verified by deep sequencing. The GGAssembler workflow is, therefore, an accurate approach for generating complex variant libraries that may drastically reduce costs and accelerate discovery and optimization of antibodies, enzymes and other proteins. The workflow is accessible through a Google Colab notebook at https://github.com/Fleishman-Lab/GGAssembler.

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Publication Details

Journal
Protein Science
Published
2024-09-16
DOI
https://doi.org/10.1002/pro.5169
Citations
3
Primary Topic
Genomics and Phylogenetic Studies
Type
article
Field-Weighted Citation Impact
0.70

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article

GGAssembler: Precise and economical design and synthesis of combinatorial mutation libraries

Shlomo Yakir Hoch, Sarel Jacob Fleishman, Jonathan J. Weinstein, Ravit Netzer et al.
3 citations
Protein Science
Genomics and Phylogenetic Studies
0.70
article

GGAssembler: Precise and economical design and synthesis of combinatorial mutation libraries

Shlomo Yakir Hoch, Sarel Jacob Fleishman, Jonathan J. Weinstein, Ravit Netzer, Karen Hakeny, Lucas Krauss
article en
3 citations

Abstract

Golden Gate assembly (GGA) can seamlessly generate full-length genes from DNA fragments. In principle, GGA could be used to design combinatorial mutation libraries for protein engineering, but creating accurate, complex, and cost-effective libraries has been challenging. We present GGAssembler, a graph-theoretical method for economical design of DNA fragments that assemble a combinatorial library that encodes any desired diversity. We used GGAssembler for one-pot in vitro assembly of camelid antibody libraries comprising >10<sup>5</sup> variants with DNA costs <0.007$ per variant and dropping significantly with increased library complexity. >93% of the desired variants were present in the assembly product and >99% were represented within the expected order of magnitude as verified by deep sequencing. The GGAssembler workflow is, therefore, an accurate approach for generating complex variant libraries that may drastically reduce costs and accelerate discovery and optimization of antibodies, enzymes and other proteins. The workflow is accessible through a Google Colab notebook at https://github.com/Fleishman-Lab/GGAssembler.

Protein ScienceVol. 33(10)
Weizmann Institute of Science (IL)
Volkswagen Foundation, Israel Science Foundation
Openalex Percentile: Top 30%
Genomics and Phylogenetic Studies
0.70
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<scp>GGAssembler</scp>: Precise and economical design and synthesis of combinatorial mutation libraries — Shlomo Yakir Hoch, Sarel Jacob Fleishman, et al. · Protein Science (2024) | TGRS Research Map | TGRS