Abstract

Chitosan has been widely used to prepare a DNA carrier for highly efficient and non-toxic gene therapy. In the present study, we investigated DNA charge neutralization and compaction by chitosan in solutions of various pH levels by dynamic light scattering (DLS), magnetic tweezers (MT), and atomic force microscopy (AFM). We found that when chitosan concentration is higher than a critical value (0.2 µM), corresponding the ratio of phosphate and NH2 in chitosan , the electrophoretic mobility of DNA-chitosan complex maintains an almost constant value when pH of solution is less 6.5, the isoelectric point of chitosan. Then it decreases with increasing pH of solution. However, when chitosan concentration is lower than the critical value, the mobility of the complex increases with pH in the range of acidity and reaches the maximum when the pH of the solution approaches the isoelectric point of chitosan. It finally decreases with increasing pH in solutions. The corresponding condensing force of the DNA-chitosan complex measured by single molecular MT changes accordingly with its charge neutralization in the same solution concentration (20 µM) and is consistent with the DLS measurements. This phenomenon might be related to the weakening interaction between DNA and chitosan in low pH solutions, and is verified by measuring the ratio of free chitosan to DNA complex in solutions. We also observed the various morphologies of DNA-chitosan complexes, such as ring, rod, flower, braid, and other structures, under different degrees of deacetylation, molecular weight, solution concentration and pH in solutions by AFM.

Highlights

  • DNA is a negatively-charged long-chain organic polymer

  • We investigated the electrostatic, mechanical features, and morphology of chitosan-DNA complexes by dynamic light scattering (DLS), single molecular magnetic tweezers (MT), and atomic force microscopy (AFM)

  • We use MP-285 to move the magnet slowly away to lower the force to a needed value to pH in solutions, we can see the electrophoretic mobility (EM) of the chitosan-DNA complex changes slowly at high chitosan observe the conformational change of DNA

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Summary

Introduction

DNA is a negatively-charged long-chain organic polymer. In a living cellular system, DNA molecules are confined into a small space that contains proteins and various small ions to compensate the negative charge of DNA to overcome Coulombic repulsion. The long-chain molecules are highly packed in various organisms from viruses to eukaryotic cells in order to store, transport and preserve the genetic material. DNA is compacted into chromatin by combining with positively-charged histones in the nuclear matrix of nucleus in eukaryotic cells [1]. Understanding DNA compaction involving like-charge attraction is important for fundamental biological processes such as chromosome assembly. We need an effective transfection vector that is able to compact DNA, protect it against degradation, and deliver

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