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Updated: Jun 27, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
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Programmable Hierarchical Assembly of Atomically Precise Metal Nanoclusters Using Supra-Amphiphilic Nucleic Acids.

Gaoang Zhou1, Siyuan Zhang1,2, Yan Zhou1

  • 1State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules and National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai 200240, China.

JACS Au
|June 26, 2026
PubMed
Summary

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This summary is machine-generated.

Researchers developed a novel method for creating self-assembling, amphiphilic nucleic acids using gold nanoclusters. This breakthrough enables the construction of versatile functional nanomaterials for diverse applications.

Area of Science:

  • Nanotechnology
  • Supramolecular Chemistry
  • Materials Science

Background:

  • Amphiphilic nucleic acids are key for creating functional nanosystems.
  • Current methods rely on covalent conjugation, limiting design flexibility.
  • Noncovalent assembly of amphiphilic nucleic acid architectures is a significant challenge.

Purpose of the Study:

  • To develop a noncovalent strategy for assembling supra-amphiphilic nucleic acids.
  • To create tunable, self-assembling nanomaterials using gold nanoclusters and DNA.
  • To establish a versatile platform for advanced nanomaterial construction.

Main Methods:

  • Utilized partially phosphorothioate-modified single-stranded DNA and gold nanoclusters (Au NCs) as building blocks.
  • Assembly driven by hydrophobic interactions and coordination between DNA and Au NCs.
Keywords:
DNA origamihierarchical assemblymetal nanoclustersingle-stranded DNAsupra-amphiphiles

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Last Updated: Jun 27, 2026

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  • Tuned micelle size by modulating the hydrophilic DNA segment length in the presence of Mg2+.
  • Main Results:

    • Successfully assembled supra-amphiphilic nucleic acids via noncovalent interactions.
    • Created well-defined micelles with tunable sizes through self-assembly.
    • Demonstrated programmable higher-order assembly via DNA hybridization and DNA origami scaffolds.

    Conclusions:

    • Established a versatile, noncovalent platform for constructing functional nanomaterials.
    • Enabled programmable supramolecular assembly of DNA-nanocluster hybrids.
    • Opened new avenues for applications in catalysis, bioimaging, and nanodevices.