Allostery of DNA nanostructures controlled by enzymatic modifications. Issue 13 (11th June 2020)

• Record Type: Journal Article
• Authors: Yan, Qi; Wang, Yaqi; Shi, Jile; Wei, Bryan
• Is Part Of: Nucleic acids research. Volume 48:Issue 13(2020)
• Page Start: 7595
• Page End: 7600
• Publication Date: 2020-06-11
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkaa488
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: Allostery is comprehensively studied for natural macromolecules, such as proteins and nucleic acids. Here, we present controllable allostery of synthetic DNA nanostructure–enzyme systems. Rational designs of the synthetic allosteric systems are based on an in-depth understanding of allosteric sites with several types of strand placements, whose varying stacking strengths determine the local conformation and ultimately lead to a gradient level of allosteric transition. When enzymes in a molecular cloning toolbox such as DNA polymerase, exonuclease and ligase are applied to treat the allosteric sites, the resulting local conformational changes propagate through the entire structure for a global allosteric transition.