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Application of multiple response optimization design to quantum dot-encoded microsphere bioconjugates hybridization assay

机译:多重响应优化设计在量子点编码微球生物缀合物杂交检测中的应用

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摘要

The optimization of DNA hybridization for genotyping assays is a complex experimental problem that depends on multiple factors such as assay formats, fluorescent probes, target sequence, experimental conditions, and data analysis. Quantum dot-doped particle bioconjugates have been previously described as fluorescent probes to identify single nucleotide polymorphisms even though this advanced fluorescent material has shown structural instability in aqueous environments. To achieve the optimization of DNA hybridization to quantum dot-doped particle bioconjugates in suspension while maximizing the stability of the probe materials, a nonsequential optimization approach was evaluated. The design of experiment with response surface methodology and multiple optimization response was used to maximize the recovery of fluorescent probe at the end of the assay simultaneously with the optimization of target-probe binding. Hybridization efficiency was evaluated by the attachment of fluorescent oligonucleotides to the fluorescent probe through continuous flow cytometry detection. Optimal conditions were predicted with the model and tested for the identification of single nucleotide polymorphisms. The design of experiment has been shown to significantly improve biochemistry and biotechnology optimization processes. Here we demonstrate the potential of this statistical approach to facilitate the optimization of experimental protocol that involves material science and molecular biology.
机译:用于基因分型分析的DNA杂交优化是一个复杂的实验问题,它取决于多种因素,例如测定形式,荧光探针,靶序列,实验条件和数据分析。量子点掺杂的粒子生物共轭物先前已被描述为荧光探针,可识别单核苷酸多态性,即使这种先进的荧光材料在水性环境中显示出结构不稳定。为了实现与悬浮液中量子点掺杂颗粒生物共轭物的DNA杂交的优化,同时最大化探针材料的稳定性,我们评估了一种非顺序优化方法。使用响应面方法和多重优化响应的实验设计,可以在分析结束时与目标探针结合优化同时最大化荧光探针的回收率。通过连续流式细胞术检测荧光寡核苷酸与荧光探针的连接来评估杂交效率。用该模型预测最佳条件并测试其鉴定单核苷酸多态性。实验设计已显示出可显着改善生物化学和生物技术优化过程。在这里,我们证明了这种统计方法有助于优化涉及材料科学和分子生物学的实验方案的潜力。

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