Structural Expansion of Catalytic RNA Nanostructures through Oligomerization of a Cyclic Trimer of Engineered Ribozymes

Author:

Siddika Mst. Ayesha1ORCID,Oi Hiroki2,Hidaka Kumi3,Sugiyama Hiroshi4ORCID,Endo Masayuki45,Matsumura Shigeyoshi12,Ikawa Yoshiya12ORCID

Affiliation:

1. Graduate School of Innovative Life Science, University of Toyama, Toyama 930-8555, Toyama, Japan

2. Department of Chemistry, Graduate School of Science and Engineering, University of Toyama, Toyama 930-8555, Toyama, Japan

3. Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8501, Kyoto, Japan

4. Institute for Integrated Cell-Material Sciences, Kyoto University, Kyoto 606-8501, Kyoto, Japan

5. Organization for Research and Development of Innovative Science and Technology, Kansai University, Suita 564-8680, Osaka, Japan

Abstract

The multimolecular assembly of three-dimensionally structured proteins forms their quaternary structures, some of which have high geometric symmetry. The size and complexity of protein quaternary structures often increase in a hierarchical manner, with simpler, smaller structures serving as units for larger quaternary structures. In this study, we exploited oligomerization of a ribozyme cyclic trimer to achieve larger ribozyme-based RNA assembly. By installing kissing loop (KL) interacting units to one-, two-, or three-unit RNA molecules in the ribozyme trimer, we constructed dimers, open-chain oligomers, and branched oligomers of ribozyme trimer units. One type of open-chain oligomer preferentially formed a closed tetramer containing 12 component RNAs to provide 12 ribozyme units. We also observed large assembly of ribozyme trimers, which reached 1000 nm in size.

Funder

University of Toyama Discretionary Funds of the President

MEXT KAKENHI

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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