Capturing and stabilizing folded proteins in lattices formed with branched oligonucleotide hybrids

Schwenger, Alexander, Jurkowski, Tomasz P ORCID: https://orcid.org/0000-0002-2012-0240 and Richert, Clemens 2018. Capturing and stabilizing folded proteins in lattices formed with branched oligonucleotide hybrids. ChemBioChem 19 (14) , pp. 1523-1530. 10.1002/cbic.201800145

Preview

PDF - Accepted Post-Print Version Download (2MB) | Preview

Abstract

The encapsulation of folded proteins in stabilizing matrices is one of the challenges of soft‐matter materials science. Capturing such fragile bio‐macromolecules from aqueous solution, and embedding them in a lattice that stabilizes them against denaturation and decomposition is difficult. Here, we report that tetrahedral oligonucleotide hybrids as branching elements, and connecting DNA duplexes with sticky ends can assemble into materials. The material‐forming property was used to capture DNA‐binding proteins selectively from aqueous protein mixtures. The three‐dimensional networks also encapsulate guest molecules in a size‐selective manner, accommodating proteins up to a molecular weight of approximately 159 kDa for the connecting duplex lengths tested. Exploratory experiments with green fluorescent protein showed that, when embedded in the DNA‐based matrix, the protein is more stable toward denaturation than in the free form, and retains its luminescent properties for at least 90 days in dry form. The noncrystalline biohybrid matrices presented herein may be used for capturing other proteins or for producing functional materials.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Biosciences
Publisher:	Wiley
ISSN:	1439-4227
Date of First Compliant Deposit:	18 February 2019
Date of Acceptance:	10 June 2018
Last Modified:	23 Nov 2024 09:30
URI:	https://orca.cardiff.ac.uk/id/eprint/119001

Citation Data

Cited 2 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item