Multiphoton lithography with protein photoresists

被引:2
作者
Sivun, Dmitry [1 ]
Murtezi, Eljesa [1 ]
Karimian, Tina [1 ]
Hurab, Kurt [1 ]
Marefat, Maryam [1 ]
Klimareva, Elena [1 ]
Naderer, Christoph [1 ]
Buchroithner, Boris [1 ]
Klar, Thomas A. [2 ]
Gvindzhiliia, Georgii [2 ]
Horner, Andreas [3 ]
Jacak, Jaroslaw [1 ,4 ]
机构
[1] Univ Appl Sci Upper Austria, Dept Med Engn, Garnisonstra 21, A-4020 Linz, Austria
[2] Johannes Kepler Univ Linz, Inst Appl Phys, Altenberger Str 69, A-4040 Linz, Austria
[3] Johannes Kepler Univ Linz, Inst Biophys, Gruberstr 40, A-4020 Linz, Austria
[4] Ludwig Boltzmann Inst Expt & Clin Traumatol, AUVA Res Ctr, Donaueschingenstr 13, A-1200 Vienna, Austria
关键词
Multiphoton lithography; Protein printing; Functional photoresist; Tissue scaffolds; Extracellular vesicle; BOVINE SERUM-ALBUMIN; 2-PHOTON POLYMERIZATION; HYALURONIC-ACID; HYDROGELS; FABRICATION; POLYMERS; MICROSTRUCTURES; STREPTAVIDIN; TECHNOLOGY; ELASTICITY;
D O I
10.1016/j.mtbio.2024.100994
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Recently, 2D/3D direct laser writing has attracted increased attention due to its broad applications ranging from biomedical engineering to aerospace. 3D nanolithography of water-soluble protein-based scaffolds have been envisioned to provide a variety of tunable properties. In this paper, we present a functional protein-based photoresist with tunable mechanical properties that is suitable for multiphoton lithography (MPL). Through the use of methacrylated streptavidin or methacrylated bovine serum albumin in combination with polyethylene glycol diacrylate or methacrylated hyaluronic acid as crosslinkers and a vitamin-based photoinitiator, we were able to write two- and three-dimensional structures as small as 200 nm/600 nm lateral/axial features, respectively. We also demonstrated that Young's modulus can be tuned by the photoresist composition, and we were able to achieve values as low as 40 kPa. Furthermore, we showed that Young's modulus can be recovered after drying and rehydration (i.e. shelf time determination). The retained biological functionality of the streptavidin scaffolds was demonstrated using fluorescently labelled biotins. Using single-molecule fluorescence microscopy, we estimated the density of streptavidin in the written features (1.8 +/- 0.2 x 105 streptavidins per 1.00 +/- 0.05 mu m3 of feature volume). Finally, we showed applicability of our 2D scaffold as a support for a fluorescence absorbance immuno-assay (FLISA), and as a delivery platform of extracellular vesicles to HeLa cells.
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页数:9
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