QIBEBT Developes Biomimetic Oligopeptide-directed Self-assembly of Functional Molecules

Jun 16, 2014     Email"> PrintText Size

Biomacromolecules, such as deoxyribonucleic acid (DNA), protein, and carbohydrate etc., can form well-organized, high ordered nanostructures, which plays an important role in the functionalization of organisms. The construction of biobased materials by taking advantage of the well-organized hierarchical nanostructures and the biocompatibility of biomolecules has been attracting much attention.  

Prof. WAN Xiaobo’s group from CAS Key Laboratory of Biobased Materials has synthesized biomimetic oligopeptides which can form b-sheet structures and further investigated the peptide-directed self-assembly of functional molecules, especially the conjugated semiconductors. The results have been published in Supramolecular Chemistry, Macromolecular Chemistry and Physics, and Soft Matter. 

Figure 1. Gly-Val-Gly-Val and the chiral fibers

Gly-Val-Gly-Val and quaterthiophene, the nanostructures can be manipulated by changing the molecular weight, low-molecular-weight polymer assembled into thick fibers, and the high-molecular-weight polymers formed spherical particles (Figure 4, Macromolecular Chemistry and Physics, 2014, 215(9), 906-914).

Figure 2. Conjugates of Gly-Val-Gly-Val with oligothiophene

It was found that Gly-Val-Gly-Val can regulate the nanostructures of oligothiophene that was attached onto it. The Peptide/oligothiophene content ratio and location of the peptide greatly affect the nanostructures and properties of the assemblies, and also the supramolecular chirality (Figure 2, Supramolecular Chemistry, 2014, 26(5-6), 383-391).  

The conjugate of Gly-Val-Gly-Val peptide and dithienylcyclopentene was also prepared. It forms an organogel in Tetrahydrofuran (THF). This organogel is multi-responsive to various external stimuli including temperature, light, chemical, and mechanical force. Moreover, in the presence of catechol, this gelator forms a more robust organogel, accompanied with a dramatic change of the assembly manner and rheological properties (Figure 3, Soft Matter, 2013, 9, 7538-7544). 

Figure 3. Conjugates of Gly-Val-Gly-Val with dithienylcyclopentene

In addition, Gly-Val-Gly-Val can regulate the nanostructures of polymers. For the alternative copolymers of When Gly-Val-Gly-Val was decorated to the polythiophenes as side chains, the polymers can form uniform nanorods (Figure 5, Supramolecular Chemistry, 2013, 25(12), 842-847). Gly-Val-Gly-Val segment which can easily form anti-parallel b-sheets was prepared via solution-phase peptide synthesis technology. Such oligopeptide can self-assemble into helical nanofibers. The driving force of the self-assembly of this biomimetic peptide are the H-bonds and the azide-azide interactions between adjacent molecules (Figure 1, Supramolecular Chemistry 2013, 25(5), 269-275). 

Figure 4. Alternative copolymers of Gly-Val-Gly-Val and quaterthiophene

Figure 5. Polythiophene decorated with Gly-Val-Gly-Val as side chains  (All Images by Prof. WAN's group)

These researches were conducted by Prof. WAN Xiaobo from CAS, Key Laboratory of Biobased Materials, QIBEBT, and supported by the National Natural Science Foundation of China and the Hundred-Talent-Project, Chinese Academy of Sciences. 

Reference:

1.       Supramolecular Chemistry 2013, 25(5), 269-275.  

2.       Supramolecular Chemistry 2014, 26(5-6), 383-391.  　  

3.       Soft Matter 2013, 9, 7538-7544. 

4.       Macromolecular Chemistry and Physics 2014, 215(9), 906-914.  

5.       Supramolecular Chemistry 2013, 25(12), 842-847.  

Contact: 
Prof. WAN Xiaobo 
E-mail: wanxb (AT) qibebt.ac.cn  
Web: http://english.qibebt.cas.cn