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用于特定细胞附着和图案化的DNA功能化蜘蛛丝纳米水凝胶

DNA Functionalized Spider Silk Nanohydrogels for Specific Cell Attachment and Patterning.

作者信息

Heinritz Christina, Lamberger Zan, Kocourková Karolína, Minařík Antonín, Humenik Martin

机构信息

Department of Biomaterials, Faculty of Engineering Science, Universität Bayreuth, Prof.-Rüdiger-Bormann.Str. 1, 95447 Bayreuth, Germany.

Department of Physics and Materials Engineering, Tomas Bata University in Zlín, Vavrečkova 275, 76001 Zlín, Czech Republic.

出版信息

ACS Nano. 2022 May 24;16(5):7626-7635. doi: 10.1021/acsnano.1c11148. Epub 2022 May 6.

Abstract

Nucleated protein self-assembly of an azido modified spider silk protein was employed in the preparation of nanofibrillar networks with hydrogel-like properties immobilized on coatings of the same protein. Formation of the networks in a mild aqueous environment resulted in thicknesses between 2 and 60 nm, which were controlled only by the protein concentration. Incorporated azido groups in the protein were used to "click" short nucleic acid sequences onto the nanofibrils, which were accessible to specific hybridization-based modifications, as proved by fluorescently labeled DNA complements. A lipid modifier was used for efficient incorporation of DNA into the membrane of nonadherent Jurkat cells. Based on the complementarity of the nucleic acids, highly specific DNA-assisted immobilization of the cells on the nanohydrogels with tunable cell densities was possible. Addressability of the DNA cell-to-surface anchor was demonstrated with a competitive oligonucleotide probe, resulting in a rapid release of 75-95% of cells. In addition, we developed a photolithography-based patterning of arbitrarily shaped microwells, which served to spatially define the formation of the nanohydrogels. After detaching the photoresist and PEG-blocking of the surface, DNA-assisted immobilization of the Jurkat cells on the nanohydrogel microstructures was achieved with high fidelity.

摘要

利用叠氮基修饰的蜘蛛丝蛋白的有核蛋白自组装,制备具有水凝胶样特性的纳米纤维网络,并将其固定在相同蛋白的涂层上。在温和的水性环境中形成的网络厚度在2至60纳米之间,其仅由蛋白质浓度控制。蛋白质中引入的叠氮基用于将短核酸序列“点击”到纳米纤维上,荧光标记的DNA互补物证明,这些纳米纤维可进行基于特异性杂交的修饰。使用脂质修饰剂将DNA有效整合到非贴壁Jurkat细胞的膜中。基于核酸的互补性,能够以可调的细胞密度将细胞高度特异性地DNA辅助固定在纳米水凝胶上。用竞争性寡核苷酸探针证明了DNA细胞到表面锚定的可寻址性,导致75-95%的细胞快速释放。此外,我们开发了一种基于光刻的任意形状微孔图案化方法,用于在空间上定义纳米水凝胶的形成。去除光刻胶并对表面进行聚乙二醇封闭后,Jurkat细胞以高保真度被DNA辅助固定在纳米水凝胶微结构上。

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