Miduturu Chandrasekhar V, Silverman Scott K
Department of Chemistry, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, Illinois 61801, USA.
J Am Chem Soc. 2005 Jul 27;127(29):10144-5. doi: 10.1021/ja051950t.
We report that double-helical DNA constraints can be used to control the conformation of another molecule, RNA. When a covalently attached DNA constraint is structurally incompatible with the native Mg2+-dependent RNA conformation, RNA folding is disrupted, as revealed by nondenaturing gel electrophoresis and independently by chemical probing. Our approach is distinct from other efforts in DNA nanotechnology, which have prepared DNA objects by self-assembly, built static DNA lattices for assembly of other objects, and created nanomachines made solely of DNA. In contrast, our dynamic use of DNA to control the conformations of other macromolecules should have wide impact in nanotechnology applications ranging from materials science to biology.
我们报告称,双螺旋DNA限制可用于控制另一种分子RNA的构象。当共价连接的DNA限制在结构上与天然的Mg2+依赖型RNA构象不相容时,RNA折叠会被破坏,这通过非变性凝胶电泳以及独立的化学探针检测得以揭示。我们的方法不同于DNA纳米技术中的其他研究,那些研究通过自组装制备DNA物体,构建静态DNA晶格用于其他物体的组装,以及制造仅由DNA构成的纳米机器。相比之下,我们动态利用DNA来控制其他大分子的构象,在从材料科学到生物学的纳米技术应用中应会产生广泛影响。