Tissue Engineering and Biofabrication Laboratory, Department of Health Sciences and Technology, ETH Zürich, Zürich, Switzerland.
Laboratory of Stem Cell Bioengineering, School of Life Sciences and School of Engineering, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Adv Mater. 2020 Jun;32(25):e1908299. doi: 10.1002/adma.201908299. Epub 2020 May 11.
Three-dimensional (3D) control over the placement of bioactive cues is fundamental to understand cell guidance and develop engineered tissues. Two-photon patterning (2PP) provides such placement at micro- to millimeter scale, but nonspecific interactions between proteins and functionalized extracellular matrices (ECMs) restrict its use. Here, a 2PP system based on nonfouling hydrophilic photocages and Sortase A (SA)-based enzymatic coupling is presented, which offers unprecedented orthogonality and signal-to-noise ratio in both inert hydrogels and complex mammalian matrices. Improved photocaged peptide synthesis and protein functionalization protocols with broad applicability are introduced. Importantly, the method enables 2PP in a single step in the presence of fragile biomolecules and cells, and is compatible with time-controlled growth factor presentation. As a corollary, the guidance of axons through 3D-patterned nerve growth factor (NGF) within brain-mimetic ECMs is demonstrated. The approach allows for the interrogation of the role of complex signaling molecules in 3D matrices, thus helping to better understand biological guidance in tissue development and regeneration.
三维(3D)控制生物活性线索的位置对于理解细胞导向和开发工程组织至关重要。双光子图案化(2PP)在微到毫米的范围内提供了这种定位,但蛋白质与功能化细胞外基质(ECM)之间的非特异性相互作用限制了其使用。本文提出了一种基于非粘连亲水性光笼和基于 Sortase A(SA)的酶偶联的 2PP 系统,该系统在惰性水凝胶和复杂的哺乳动物基质中提供了前所未有的正交性和信噪比。引入了具有广泛适用性的改进的光笼肽合成和蛋白质功能化方案。重要的是,该方法能够在脆弱的生物分子和细胞存在的情况下一步实现 2PP,并且与时间控制的生长因子呈现兼容。作为推论,通过脑模拟 ECM 中的 3D 图案神经生长因子(NGF)引导轴突。该方法允许在 3D 基质中询问复杂信号分子的作用,从而有助于更好地理解组织发育和再生中的生物导向。