文献类型：期刊文献

英文题名：Synthesis of Water Soluble Quantum Dots for Monitoring Carrier-DNA Nanoparticles in Plant Cells

作者：Wang, Qiong[1] Chen, Jienan[1,2] Zhang, Huaiyun[1] Lu, Mengzhu[3] Qiu, Deyou[3] Wen, Yafeng[1] Kong, Qianqian[1]

第一作者：Wang, Qiong

通信作者：Chen, JN[1]

机构：[1]Cent S Univ Forestry & Technol, Inst Biol & Environm Sci & Technol, Changsha 410004, Hunan, Peoples R China;[2]Transpoints Inc, Gainesville, FL 32614 USA;[3]Chinese Acad Forestry, Res Inst Forestry, Beijing 100091, Peoples R China

年份：2011

卷号：11

期号：3

起止页码：2208-2214

外文期刊名：JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000288102300054)】；

基金：This work was supported by a grant from the National High Technology Research and Development Program of China (No. 2007AA10Z182) and a grant from the China Special Research Program for Public Benefit Industries (No. 200904038).

语种：英文

外文关键词：Quantum Dot; L-Cysteine; Bio-Labels; Nano-Scale Carriers; Jatropha Curcas

摘要：Fluorescent quantum dots (QDs) have shown great promise for use as biolabels in cell and animal biology and more recently in plant sciences. An important use of QDs is for monitoring the dynamics, intracellular trafficking, and fate of carrier-DNA nanocomplexes in cell transfection and potentially in plant transformation. In this study, a low cost aqueous procedure has been developed to efficiently prepare biocompatible QDs for monitoring nanoparticle-mediated gene transfer in conjunction with molecular breeding of Jatropha curcas. Water-soluble CdSe nanoparticles were synthesized by self-assembly using L-Cysteine as stabilizer and optimal synthesis scheme established by fluorescence spectroscopy. The QDs were used to label chitosan-DNA nanoparticles via electrostatic interaction and the resultant QD-labeled chitosan-DNA complexes were shown to have superior fluorescence properties with red shift of emission and absorption spectra relative to the CdSe QDs alone. This system is being explored as a superior alternative to Agrobacterium-mediated genetic transformation of Jatropha curcas cells. PCR amplification of the full length of the carried reporter gene (GFP) suggests that the DNA was not digested in Jatropha curcas cells transfected with CdSe/CS-DNA complexes. Furthermore, GFP gene expression in the transfected callus cells, as evidenced by fluorescence detection, suggests that the target DNA was integrated into the plant genome.