4.6 Article

Effect of Peptide Sequences on Supramolecular Interactions of Naphthaleneimide/Tripeptide Conjugates

Journal

LANGMUIR
Volume 32, Issue 30, Pages 7630-7638

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.6b01809

Keywords

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Funding

  1. Ministry of Science and Technology of the Republic of China, Taiwan [MOST 104-2119-M-009-006]
  2. Aim for the Top University program of the National Chiao Tung University
  3. Ministry of Education, Taiwan, R.O.C.
  4. Novel Bioengineering and Technological Approaches to Solve Two Major Health Problems in Taiwan - Taiwan Ministry of Science and Technology Academic Excellence Program [MOST 105-2633-B-009-003]
  5. National Center for High-Performance Computing of Taiwan

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In this study, we reported a significant difference in the supramolecular hydrogelation of newly discovered NI-GFF (NI-Gly-L-Phe-L-Phe) and NI-FFG (NI-L-Phe-L-Phe-Gly) on the basis of their phase diagrams. With a small difference in the peptide chain between NI-GFF and NI-FFG, we observed a significant difference in their self-assembly properties; NI-GFF formed a stable gel at neutral pH, whereas NI-FFG did not, under the same conditions. From spectroscopic and computational studies, intermolecular pi-pi interactions and extended hydrogen bonding interactions might reinforce the intermolecular interactions of NI-GFF, which may facilitate the formation of the self-assembled nanostructures and the hydrogel. In addition, the aggregation-induced emission (AIE)-active NI-GFF reveals relatively good biocompatibility compared with that of NI-FFG for two commonly used cell lines, suggesting that it is a promising candidate for use as a supramolecular material in biomedical applications. Our results highlight the importance of tripeptide sequences in a self-assembling hydrogel system.

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