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Peptide induces chirality evolution in a single gold nanoparticle

New bioinspired optical materials for flexible, reflective display

Date:
April 18, 2018
Source:
Seoul National University
Summary:
Scientists have created a synthesis method to make optically active and chiral gold nanoparticles using amino acids and peptides for the first time. Many chemicals significant to life have mirror-imaged twins and such characteristics are conventionally called as chirality. This study describes how the chirality, typically observed in organic molecules, can be extended to three-dimensional metallic nanostructures. The research will be published in Nature and featured in its cover.
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For the first time, scientists have successfully created optically active, chiral gold nanoparticles using amino acids and peptides. Many chemicals significant to life have mirror-image twins (left-handed and right-handed structures), a characteristic that is conventionally called chirality. This study describes how chirality, which is typically observed in organic molecules, can be extended to three-dimensional metallic nanostructures. This newly discovered synthesis method was described in Nature (April 19th) and was featured on the cover.

The Korean research teams at Seoul National University (SNU), Pohang University of Science and Technology (POSTECH) and LG Display (LGD) demonstrated the direct transfer of peptide handedness to nanoparticles' morphology during their growth. Mirror-image peptide twins induced the opposite twist of the chiral nanoparticles, which are further tunable with sequence variation. The chiral gold nanoparticles with different handedness interacted differently with circularly polarized visible light, displaying extensive color modulation. As a result, color change is possible by controlling the light polarization, which has potential applications in future displays.

In newly synthesized gold nanoparticles, chiral elements are arranged on cube-like structures with a side length of only about 100 nm. They can be easily dispersed in solutions and deposited on the substrates while maintaining high chiro-optical activities.

"Based on our understanding of the interface between peptides and inorganic materials, we have built a new platform technology to control the crystallographic asymmetry," explains Professor Ki Tae Nam at SNU, who led this collaborative project. He added, "This finding can make a direct and immediate impact on optical devices and could be further applied for the development of enantioselective bioinspired catalysts in the near future."

"The potential applications include active color displays, holography, chirality sensors and all-angle negative refractive index materials," explained Professor Junsuk Rho at POSTECH, the co-corresponding author.


Story Source:

Materials provided by Seoul National University. Note: Content may be edited for style and length.


Journal Reference:

  1. Hye-Eun Lee, Hyo-Yong Ahn, Jungho Mun, Yoon Young Lee, Minkyung Kim, Nam Heon Cho, Kiseok Chang, Wook Sung Kim, Junsuk Rho, Ki Tae Nam. Amino-acid- and peptide-directed synthesis of chiral plasmonic gold nanoparticles. Nature, 2018; 556 (7701): 360 DOI: 10.1038/s41586-018-0034-1

Cite This Page:

Seoul National University. "Peptide induces chirality evolution in a single gold nanoparticle." ScienceDaily. ScienceDaily, 18 April 2018. <www.sciencedaily.com/releases/2018/04/180418162751.htm>.
Seoul National University. (2018, April 18). Peptide induces chirality evolution in a single gold nanoparticle. ScienceDaily. Retrieved November 20, 2024 from www.sciencedaily.com/releases/2018/04/180418162751.htm
Seoul National University. "Peptide induces chirality evolution in a single gold nanoparticle." ScienceDaily. www.sciencedaily.com/releases/2018/04/180418162751.htm (accessed November 20, 2024).

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