Programmable allosteric DNA regulations for molecular networks and nanomachines

Author:

Zhang Cheng1ORCID,Ma Xueying23ORCID,Zheng Xuedong4ORCID,Ke Yonggang56ORCID,Chen Kuiting2ORCID,Liu Dongsheng7ORCID,Lu Zuhong8ORCID,Yang Jing2ORCID,Yan Hao910ORCID

Affiliation:

1. School of Computer Science, Key Lab of High Confidence Software Technologies, Peking University, Beijing 100871, China.

2. School of Control and Computer Engineering, North China Electric Power University, Beijing 102206, China.

3. Bio-evidence Sciences Academy, Xi’an Jiaotong University, Xi’an, Shaanxi 710049, China.

4. College of Computer Science, Shenyang Aerospace University, Shenyang 110136, China.

5. Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Emory University School of Medicine, Atlanta, GA 30322, USA.

6. Department of Chemistry, Emory University, Atlanta, GA 30322, USA.

7. Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education, Department of Chemistry, Tsinghua University, Beijing 100084, China.

8. The State Key Laboratory of Bioelectronics, Southeast University, Nanjing 211189, China.

9. Center for Molecular Design and Biomimetics, The Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA.

10. School of Molecular Sciences, Arizona State University, Tempe, AZ 85287, USA.

Abstract

Structure-based molecular regulations have been widely adopted to modulate protein networks in cells and recently developed to control allosteric DNA operations in vitro. However, current examples of programmable allosteric signal transmission through integrated DNA networks are stringently constrained by specific design requirements. Developing a new, more general, and programmable scheme for establishing allosteric DNA networks remains challenging. Here, we developed a general strategy for programmable allosteric DNA regulations that can be finely tuned by varying the dimensions, positions, and number of conformational signals. By programming the allosteric signals, we realized fan-out/fan-in DNA gates and multiple-layer DNA cascading networks, as well as expanding the approach to long-range allosteric signal transmission through tunable DNA origami nanomachines ~100 nm in size. This strategy will enable programmable and complex allosteric DNA networks and nanodevices for nanoengineering, chemical, and biomedical applications displaying sense-compute-actuate molecular functionalities.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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