Silver Nanoparticles Accelerated DNA Assembly Severalfold

14:46
Assembling long DNA chains from short pieces is a routine but finicky procedure in biotechnology. Classical restriction enzymes leave short “sticky” ends, and fragments do not join very readily. Product yield often remains low.

A team from Nagoya University proposed a different tool—silver nanoparticles. They cause site-specific cleavage of chemically modified oligonucleotides. Under optimized conditions (with a polyethylene glycol coating, at 50 °C), cleavage efficiency exceeded 91% within 1–2 hours. By comparison, silver ions alone produced a yield of only about 14%.

The main advantage is the length of the sticky ends. The method makes it possible to obtain segments of 8 or even 18 bases. With eight-base ends, ligation proceeded about twice as efficiently as usual. With eighteen-base ends—almost fivefold (44% versus 8%). In addition, the nanoparticles retained unwanted cut-off fragments, so the pure product could be recovered with yields of up to 98%.

To verify functionality, the researchers assembled a fragment encoding green fluorescent protein (GFP) and introduced it into HeLa cells. The protein was expressed—meaning the assembly proceeded accurately and without critical errors.

For now, this is a laboratory protocol. But more reliable and faster assembly of long DNA constructs is needed for gene therapy, vaccine development, and plant engineering. Silver nanoparticles may become a convenient addition to the synthetic biology toolkit.

Sources:

  1. Nagoya University. "Japanese scientists use tiny silver particles to make DNA assembly up to 5x more efficient." ScienceDaily (August 19, 2026).
  2. Inagaki M. et al. "Silver nanoparticle-induced site-specific strand cleavage of chemically modified oligonucleotides for long-chain DNA assembly." Nucleic Acids Research (2026). DOI: 10.1093/nar/gkag525.

Author: Maksim Aleksandrovich Erdyakov

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