Photoinduced Amyloid Fibril Degradation for Controlled Cell Patterning

Kübra Kaygisiz, Adriana M. Ender, Jasmina Gačanin, L. Alix Kaczmarek, Dimitrios A. Koutsouras, Abin N. Nalakath, Pia Winterwerber, Franz J. Mayer, Hans Joachim Räder, Tomasz Marszalek, Paul W.M. Blom, Christopher V. Synatschke, Tanja Weil

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7 Citations (SciVal)

Abstract

Amyloid-like fibrils are a special class of self-assembling peptides that emerge as a promising nanomaterial with rich bioactivity for applications such as cell adhesion and growth. Unlike the extracellular matrix, the intrinsically stable amyloid-like fibrils do not respond nor adapt to stimuli of their natural environment. Here, a self-assembling motif (CKFKFQF), in which a photosensitive o-nitrobenzyl linker (PCL) is inserted, is designed. This peptide (CKFK-PCL-FQF) assembles into amyloid-like fibrils comparable to the unsubstituted CKFKFQF and reveals a strong response to UV-light. After UV irradiation, the secondary structure of the fibrils, fibril morphology, and bioactivity are lost. Thus, coating surfaces with the pre-formed fibrils and exposing them to UV-light through a photomask generate well-defined areas with patterns of intact and destroyed fibrillar morphology. The unexposed, fibril-coated surface areas retain their ability to support cell adhesion in culture, in contrast to the light-exposed regions, where the cell-supportive fibril morphology is destroyed. Consequently, the photoresponsive peptide nanofibrils provide a facile and efficient way of cell patterning, exemplarily demonstrated for A549, Chinese Hamster Ovary, and Raw Dual type cells. This study introduces photoresponsive amyloid-like fibrils as adaptive functional materials to precisely arrange cells on surfaces.

Original languageEnglish
Article number2200294
JournalMacromolecular Bioscience
Volume23
Issue number2
Early online date10 Nov 2022
DOIs
Publication statusPublished - 15 Feb 2023

Acknowledgements

K.K. and A.M.E. contributed equally to this work. The authors thank Uwe Rietzler, Qi Lu for his experimental support, Pierpaolo Moscariello for his comments, and Judith Stickdorn and Alina Heck for cell culture donation and advice. Support by the IMB Microscopy Core Facility is gratefully acknowledged.

Funding

This study was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—Projektnummer 316249678—SFB 1279 (A05, C01) and Projektnummer 441734479, the Federal Ministry of Education and Research of Germany (BMBF) in the framework of ProMatLeben Polymere InGel-NxG (FKZ: 13XP5086F) as well as Kosmogel (FKZ: 13XP5148). T.M. acknowledges the Foundation for Polish Science financed by the European Union under the European Regional Development Fund (POIR.04.04.00-00-3ED8/17). This work was supported by the Max Planck Graduate Center with the Johannes Gutenberg-Universität Mainz (MPGC). Open Access funding enabled and organized by Projekt DEAL.

Keywords

  • amyloid degradation
  • controlled cell attachment
  • patterning
  • self-assembling peptide nanofibers
  • stimuli-responsive biomaterials

ASJC Scopus subject areas

  • Biotechnology
  • Bioengineering
  • Biomaterials
  • Polymers and Plastics
  • Materials Chemistry

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