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Progress in Chemistry 2022, Vol. 34 Issue (9): 1882-1895 DOI: 10.7536/PC211206 Previous Articles   Next Articles

• Review •

Controllable Assembly of Diphenylalanine Dipeptide Micro/Nano Structure Assemblies and Their Applications

Keqing Wang1,2, Huimin Xue1, Chenchen Qin1(), Wei Cui1()   

  1. 1 Institute of Chemistry, Chinese Academy of Sciences,Beijing 100190, China
    2 National Museum of China,Beijing 100006, China
  • Received: Revised: Online: Published:
  • Contact: *e-mail: cuiwei@iccas.ac.cn(Wei Cui);gracecc1989@163.com(Chenchen Qin)
  • Supported by:
    National Natural Science Foundation of China(21961142022); National Natural Science Foundation of China(21872150); National Natural Science Foundation of China(22072160)
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In recent years, the construction of micro/nano structure assemblies by biological assembly units has been extensively studied in the fields of bio-nanotechnology and other fields. Micro/nano structure assemblies with different morphologies can be obtained by a quick and simple method such as the self-assembly of biomolecules. Diphenylalanine dipeptide and its derivatives, as a biologically active peptide in many peptide-based building blocks, have good biocompatibility and characteristic for chemical modification, biological function and simple preparation. Micro/nano-materials with different structures based on diphenylalanine and its derivatives can be obtained by controllable assembled methods. They also have wide applications in optics, mechanical engineering, electrochemical sensing and detection areas, etc. Controlled assembly of short peptides and its derivatives can be achieved by changing the assembly conditions or introducing of exogenous small molecules. This review summaries and outlooks the controllable assembly of diphenylalanine dipeptide micro/nano structure assemblies and their applications in biomedicine, biosensor, optoelectronic materials, optical waveguides and catalysis.

Contents

1 Introduction

2 Controllable assembly of dipeptide-based assemblies

2.1 Physical factors

2.2 Chemical factors

2.3 Biological factors

3 Application of dipeptide-based assemblies

3.1 Biomedicine

3.2 Biosensors

3.3 Optoelectronic materials

3.4 Optical waveguide

3.5 Catalysis

4 Conclusion and outlook

Key words: molecule assembly, diphenylalanine dipeptide, biomedicine, biosensor, optoelectronic materials
Fig. 1 Chiral self-assembly of Ferrocene-L-Phe-L-Phe-OH (Fc-FF) into rationally designed chiral nanostructures[36]
Fig. 2 Representation of light-controlled reversible gel-sol transition of non-photosensitive diphenylalanine supramolecular assembly[40]
Fig. 3 Schematic illustration of the metal ion modulated structural transformation of amyloid-derived self-assembled Fmoc-FF from the β-sheet into the superhelix and random coil[15]
Fig. 4 (a) Macroscopic and microscopic characterization of gel formed by Fmoc-FF hydrogelator; (b) Packing model of Fmoc-FF dipeptides in self-assembled hydrogels as proposed by Ulijn et al.[60]
Fig. 5 Use of FF aerogels as hemostasis materials and cryogels as waterproof materials for wound care[77]
Fig. 6 Schematic process of assembling CDP-AuNP hybrid microspheres and fabrication of ChOx/CDP-AuNP/CS/PB biosensor electrodes[88]
Fig. 7 Preparation of FF nanotube piezoelectric materials[90]
Fig. 8 (a) Chemical structures of CDP and genipin and solvent-modulated assembly of CDPG; (b) schematic of the photocurrent measurements with the photoanodes based on nanospheres and nanofibers[94]
Fig. 9 (a~c) CLSM images and (d) bright-field image of rhodamine B doped diphenylalanine branched structure. (e, f) Photoluminescence images of rhodamine B-doped diphenylalanine branched structures excited at the rod position. (g) Photoluminescence image and (h) bright-field image of rhodamine B-doped diphenylalanine branched structures excited at the tips of the branches. All the scale bars represent 20 μm[98]
Fig.10 (A) Highlighted crystal structure of fungus laccase from Trametes versicolor (PDB: 1GYC). (B) Chemical structure of CDPGA, schematic illustration of reversible transformation of nanospheres to nanochains modulating by Cu2+ and H+, and switchable enzyme-like catalytic oxidation of hydroquinone to benzoquinone[33]
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