• Title of article

    Dipeptide derived from benzylcystine forms unbranched nanotubes in aqueous solution

  • Author/Authors

    Banerji, Biswadip Department of Chemistry - CSIR-Indian Institute of Chemical Biology - Raja S.C. Mullick Road, India , Kumar Pramanik, Sumit Department of Chemistry - CSIR-Indian Institute of Chemical Biology - Raja S.C. Mullick Road, India , Pal, Uttam Department of Chemistry - CSIR-Indian Institute of Chemical Biology - Raja S.C. Mullick Road, India , Chandra Maiti, Nakul Department of Chemistry - CSIR-Indian Institute of Chemical Biology - Raja S.C. Mullick Road, India

  • Pages
    6
  • From page
    1
  • To page
    6
  • Abstract
    The essence of modern nanotechnology is manifested in the formation of well-ordered nanostructures by a process of self-association. Peptides are among the most useful building blocks for organic bionanostructures such as nanotubes, nanospheres, nanotapes, nanofibrils, and other different ordered structures at the nanoscale. Peptides are biocompatible, chemically diverse, and much more stable and can be readily synthesized on a large scale. Also, they have diverse application in biosensors, tissue engineering, drug delivery, etc. Here, we report a short cystine-based dipeptide, which spontaneously self-associates to form straight, unbranched nanotubes. Such self-assembled nanobiomaterials provide a novel possibility of designing new functional biomaterials with potential applications in nanobiotechnology. The formation of nanotubes in solution state has been demonstrated by atomic force microscopy and scanning electron microscopy. Infrared absorption and circular dichroism demonstrated the intermolecular β-sheet-like backbone hydrogen bonding in juxtaposing and stacking of aromatic side chains.
  • Keywords
    Nanotube , Dipeptide , π-π stacking , Cystine , Self-assembly
  • Journal title
    Astroparticle Physics
  • Serial Year
    2013
  • Record number

    2435973