National Key Laboratory of Micro/Nano Fabrication Technology, Research Institute of Micro/Nano Science and Technology, Shanghai Jiao Tong University, Shanghai, 200240 China.
Langmuir. 2010 May 4;26(9):6083-5. doi: 10.1021/la904014z.
Graphene oxide (GO), having a large specific surface area and abundant functional groups, provides an ideal substrate for study enzyme immobilization. We demonstrated that the enzyme immobilization on the GO sheets could take place readily without using any cross-linking reagents and additional surface modification. The atomically flat surface enabled us to observe the immobilized enzyme in the native state directly using atomic force microscopy (AFM). Combining the AFM imaging results of the immobilized enzyme molecules and their catalytic activity, we illustrated that the conformation of the immobilized enzyme is mainly determined by interactions of enzyme molecules with the functional groups of GO.
氧化石墨烯(GO)具有较大的比表面积和丰富的官能团,为研究酶固定化提供了理想的基底。我们证明,酶可以在不使用任何交联试剂和额外表面修饰的情况下轻易地固定在 GO 片上。原子级平坦的表面使我们能够直接使用原子力显微镜(AFM)观察到固定化酶的天然状态。结合固定化酶分子的 AFM 成像结果及其催化活性,我们说明了固定化酶的构象主要由酶分子与 GO 官能团的相互作用决定。