4.7 Article

Poly(ethylene glycol) Crowding as Critical Factor To Determine pDNA Packaging Scheme into Polyplex Micelles for Enhanced Gene Expression

Journal

BIOMACROMOLECULES
Volume 18, Issue 1, Pages 36-43

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.6b01247

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Funding

  1. Center of Innovation (COI) Program
  2. Precursory Research for Embryonic Science and Technology (PRESTO) in Molecular Technology and Creation of New Functions from the Japan Science and Technology Corporation (JST)
  3. Japan Society for the Promotion of Science (JSPS) through Specially Promoted Research Program
  4. Core to Core Program for A. Advanced Research Networks

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A critical role of polyethylene glycol (PEG) crowding in the packaging of plasmid DNA (pDNA) into polyplex micelles (PMs) was investigated using a series of PEG-b-poly(L-lysine) (PEG-PLys) block copolymers with varying molecular weights of both PEG and PLys segments. Rod-shaped PMs preferentially formed when the tethered PEG chains covering pDNA in a precondensed state were dense enough to overlap one another (reduced tethering density (RTD) > 1), whereas globular PMs were obtained when they were not overlapped (RTD < 1). These results submitted a scheme that steric repulsive effect of PEG regulated packaging pathways of pDNA either through folding into rod-shape or collapsing into globular depending on whether the PEG chains are overlapped or not. The rod-shaped PMs gave significantly higher gene expression efficacies in a cell-free system compared to the globular PMs, demonstrating the practical relevance of regulating packaging structure of pDNA for developing efficient gene delivery systems.

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