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利用生物分子刺激对DNA凝胶微珠进行形态操控

Morphological Manipulation of DNA Gel Microbeads with Biomolecular Stimuli.

作者信息

Okumura Shu, Nixon Hapsianto Benediktus, Lobato-Dauzier Nicolas, Ohno Yuto, Benner Seiju, Torii Yosuke, Tanabe Yuuka, Takada Kazuki, Baccouche Alexandre, Shinohara Marie, Kim Soo Hyeon, Fujii Teruo, Genot Anthony

机构信息

LIMMS, CNRS-Institute of Industrial Science, UMI 2820, University of Tokyo, Tokyo 153-8505, Japan.

Department of Bioengineering, The University of Tokyo 7-3-1 Hongo, Bunkyo, Tokyo 113-8654, Japan.

出版信息

Nanomaterials (Basel). 2021 Jan 22;11(2):293. doi: 10.3390/nano11020293.

Abstract

Hydrogels are essential in many fields ranging from tissue engineering and drug delivery to food sciences or cosmetics. Hydrogels that respond to specific biomolecular stimuli such as DNA, mRNA, miRNA and small molecules are highly desirable from the perspective of medical applications, however interfacing classical hydrogels with nucleic acids is still challenging. Here were demonstrate the generation of microbeads of DNA hydrogels with droplet microfluidic, and their morphological actuation with DNA strands. Using strand displacement and the specificity of DNA base pairing, we selectively dissolved gel beads, and reversibly changed their size on-the-fly with controlled swelling and shrinking. Lastly, we performed a complex computing primitive-A Winner-Takes-All competition between two populations of gel beads. Overall, these results show that strand responsive DNA gels have tantalizing potentials to enhance and expand traditional hydrogels, in particular for applications in sequencing and drug delivery.

摘要

水凝胶在从组织工程、药物递送、食品科学到化妆品等许多领域都至关重要。从医学应用的角度来看,能够响应特定生物分子刺激(如DNA、mRNA、miRNA和小分子)的水凝胶是非常理想的,然而,将传统水凝胶与核酸连接仍然具有挑战性。在这里,我们展示了利用液滴微流控技术生成DNA水凝胶微珠,以及利用DNA链对其形态进行驱动。利用链置换和DNA碱基配对的特异性,我们选择性地溶解凝胶珠,并通过控制溶胀和收缩实时可逆地改变其大小。最后,我们在两个凝胶珠群体之间进行了一个复杂的计算原语——胜者全得竞争。总体而言,这些结果表明,链响应性DNA凝胶具有增强和扩展传统水凝胶的诱人潜力,特别是在测序和药物递送中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b1e/7912653/d295d9656c04/nanomaterials-11-00293-g001.jpg

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