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Temperature-controlled encapsulation and release of an active enzyme in the cavity of a self-assembled DNA nanocage

机译:在自组装DNA纳米笼腔中进行温度控制的包封和释放活性酶

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摘要

We demonstrate temperature-controlled encapsulation and release of the enzyme horseradish peroxidase using a preassembled and covalently closed three-dimensional DNA cage structure as a controllable encapsulation device. The utilized cage structure was covalently closed and composed of 12 double-stranded B-DNA helices that constituted the edges of the structure. The double stranded helices were interrupted by short single-stranded thymidine linkers constituting the cage corners except for one, which was composed by four 32 nucleotide long stretches of DNA with a sequence that allowed them to fold into hairpin structures. As demonstrated by gel-electrophoretic and fluorophore-quenching experiments this design imposed a temperature-controlled conformational transition capability to the structure, which allowed entrance or release of an enzyme cargo at 37 C while ensuring retainment of the cargo in the central cavity of the cage at 4 C. The entrapped enzyme was catalytically active inside the DNA cage and was able to convert substrate molecules penetrating the apertures in the DNA lattice that surrounded the central cavity of the cage.
机译:我们演示了温度控制的封装和使用预先组装和共价封闭的三维DNA笼结构作为可控制的封装设备释放的酶辣根过氧化物酶。所利用的笼结构是共价封闭的,并由构成结构边缘的12个双链B-DNA螺旋组成。双链螺旋被构成笼角的短单链胸苷连接子打断,除了一个由四个32个核苷酸长的DNA片段组成,其序列使其可以折叠成发夹结构。正如凝胶电泳和荧光团猝灭实验所证明的那样,该设计对结构施加了温度控制的构象转变能力,从而允许酶货物在37°C进入或释放,同时确保将货物保留在笼子的中央腔中。在4°C时,捕获的酶在DNA笼子内部具有催化活性,并且能够转换穿透包围笼子中心腔的DNA晶格中的孔的底物分子。

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