Shape Control and Transfection of Self-assembled Polymer-DNA Nanoparticles
Shape Control and Transfection of Self-assembled Polymer-DNA Nanoparticles
批准号:
8244219
负责人:
Hai-Quan Mao
金额:
$24.68万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-12-15 至 2013-11-30
关键词:
Bile fluidBiliaryBiodistributionBiological ProcessCell ShapeCellsChargeComputer SimulationDNADataDependenceDiseaseDisulfidesEpithelial CellsExperimental ModelsExploratory/Developmental GrantFoundationsFutureGene DeliveryGene TransferGenesGrantHepatocyteIn VitroInfusion proceduresIntravenousInvestigationKineticsKupffer CellsLiverMethodsMicellesModelingMolecular WeightMorphologyNatureOrganPatternPhysical condensationPhysiologicalPolyethylene GlycolsPolymersProcessPropertyRattusSelf-control as a personality traitSeriesSerumShapesSolventsSurfaceSystemTechnologyTestingTissuesTransfectionViralVirionbasecell typecopolymercrosslinkdriving forcegene therapyimprovedin vivoinnovationnanoparticlenovelparticleplasmid DNApolycationretinal rodsself assemblytraffickingtransgene expressionuptake
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The overall objective of this study is to develop a mechanistic understanding of shape control of self-assembled DNA nanoparticles, and to test the hypothesis that nanoparticle shape can influence their cellular uptake, intracellular trafficking and gene delivery efficiency. Several recent studies have raised the prospect that the morphology of virus particles and various types of synthetic nanoparticles is an important determinant for their transport properties and biological functions. We have developed a method for the self-assembly of DNA-containing nanoparticles with several distinct shapes (spherical, rod-like and worm-like) similar to some viral particles for the purpose of gene transfection. Such nanoparticles are ideal systems for understanding the mechanism of DNA-induced self-assembly and the effect of nanoparticle shape on their stability, cell- nanoparticle interactions, transfection efficiency and in vivo transport kinetics. With this Exploratory Grant, we plan (1) to determine the key experimental parameters that effectively control the shape and size of nanoparticles, and to understand the mechanism of shape control in DNA condensation by PEGylated polycations using a combined experimental and computational modeling approach; and (2) to demonstrate nanoparticle shape dependence in cellular uptake, intracellular trafficking and transfection efficiency in vitro and in vivo in a liver-targeted gene delivery model. This study will provide a mechanistic understanding of the major driving forces for the self-assembly of DNA/PEG-polycation nanoparticles and identify key parameters involved in their shape control. It will offer an effective method to control the size and shape of DNA/polymer nanoparticles that can be applicable to a variety of PEGylated gene carriers in synthesizing nanoparticles with high degree of control over their shapes or morphologies.
PUBLIC HEALTH RELEVANCE: This study will provide detailed understanding on how to assemble DNA nanoparticles with controlled shape and size that mimic natural virus particles. It offers an enabling technology with the potential to markedly improve the transport properties and gene transfer efficiency of DNA/polymer nanoparticles for treating a variety of diseases through the gene therapy approach.
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