Translational Medicine Group, Cranfield Health, Cranfield University, Bedfordshire, UK.
Anal Biochem. 2011 Jul 1;414(1):23-30. doi: 10.1016/j.ab.2011.02.024. Epub 2011 Feb 23.
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.
用于基因分型检测的 DNA 杂交优化是一个复杂的实验问题,取决于多个因素,如检测形式、荧光探针、靶序列、实验条件和数据分析。量子点掺杂粒子生物缀合物以前被描述为荧光探针,以识别单核苷酸多态性,尽管这种先进的荧光材料在水环境中表现出结构不稳定。为了在悬浮液中实现量子点掺杂粒子生物缀合物的 DNA 杂交优化,同时最大限度地提高探针材料的稳定性,评估了非顺序优化方法。使用实验设计与响应面法和多个优化响应来最大化荧光探针在检测结束时的回收率,同时优化目标-探针结合。通过连续流式细胞术检测评估杂交效率,通过荧光寡核苷酸与荧光探针的附着。用模型预测最佳条件,并测试用于识别单核苷酸多态性。实验设计已被证明可以显著改善生物化学和生物技术优化过程。在这里,我们展示了这种统计方法的潜力,以促进涉及材料科学和分子生物学的实验方案的优化。