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
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