Long Oligos: Direct Chemical Synthesis of Genes with up to 1,728 Nucleotides

17 July 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The longest oligos that can be chemically synthesized using known methods are typically considered to be 200-mers. Here, we report direct synthesis of an 800-mer green fluorescent protein (GFP) gene and a 1,728-mer Φ29 DNA polymerase gene on an automated synthesizer. Key innovations that enabled the breakthrough include conducting the synthesis on the smooth surface of glass wool or glass bead rather than within the pores of traditional solid supports, and the use of the powerful catching-by-polymerization (CBP) method for the isolation of the full-length oligos from the crude mixture. Conducting the synthesis on smooth surface not only eliminated the steric hindrance that would otherwise prevent long oligo assembly, but also, surprisingly, drastically reduced the errors that commonly occur in traditional oligo synthesis. The long oligos were characterized by cloning followed by Sanger sequencing. We anticipate that the new method for long oligo synthesis will have a significant impact on projects in areas such as synthetic biology, gene editing, protein engineering, and many others.

Keywords

Oligo
DNA
Gene synthesis
Solid support
Glass wool
Glass bead
long oligo
Catching-by-polymerization
Solid phase synthesis
Sequencing
Sequence error

Supplementary materials

Title
Description
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Title
Supporting Information 1
Description
Experimental details and solid support loading calculation.
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Supporting Information 2
Description
Oligo sequencing results.
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