Engineering Phi29-DNAP Variants for Customized DNA Hydrogel Materials.

Chemistry

Institute for Biological Interfaces 1 (IBG 1), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, 76344, Eggenstein-Leopoldshafen, Germany.

Published: December 2024

AI Article Synopsis

  • DNA hydrogels have potential applications in medicine and biosensors and can be produced through a method called enzymatic rolling circle amplification (RCA) using a specific DNA polymerase, phi29.
  • The study introduces new variants of this polymerase that have improved characteristics, such as better DNA binding, stability at higher temperatures, and reduced activity that breaks down DNA, along with tags for detection purposes.
  • Evaluation of these variants showed they produced similar DNA yields and hydrogel properties, and they were able to incorporate modified nucleotides, establishing a strong method for customizing DNA hydrogels.

Article Abstract

DNA hydrogels, which hold potential for use in medicine, biosensors, and tissue engineering, can be produced through enzymatic rolling circle amplification (RCA) using phi29 DNA polymerase (DNAP). This paper introduces new DNAP variants designed for RCA-based DNA hydrogel production, featuring enzymes with modified DNA binding, enhanced thermostability, reduced exonuclease activity, and protein tags for fluorescence detection or specific immobilization. We evaluated these enzymes by quantifying DNA output via quantitative PCR (qPCR) and assessing hydrogel mechanical properties through micromechanical indentation. The results showed that most variants generated similar DNA amounts and hydrogels with comparable mechanical properties. Additionally, all variants successfully incorporated non-natural nucleotides, such as base-modified dGTP derivatives and 2'fluoro-dGTP, during RCA. This study's robust analytical approach offers a strong foundation for selecting new enzymes and producing DNA hydrogels with tailored material properties.

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Source
http://dx.doi.org/10.1002/chem.202403047DOI Listing

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