串联质谱法
化学
胎儿
DNA
计算生物学
胎儿游离DNA
指纹(计算)
DNA测序
产前诊断
DNA分析
质谱法
分离(微生物学)
色谱法
微卫星
串联
DNA提取
鉴定(生物学)
聚合酶链反应
妊娠期
遗传学
杂交探针
周转时间
作者
Fei Zhu,Yimeng Qiao,Xinyi Guo,Xin Li,Qi Li,Lanlan Zhang,Zhenhua Zhao,T. Wang,L He,K. Wang,Yuhong Hu,Zhen Shao,X D Kong,Tongchuan Li,Qinghe Xing,Feng Zhou
标识
DOI:10.1021/acs.analchem.5c06012
摘要
Noninvasive prenatal testing for single-gene disorders faces significant challenges due to low fetal DNA abundance in maternal blood, particularly in early gestation. Although next-generation sequencing (NGS) is widely used, it frequently encounters false-negative outcomes and high costs when detecting low-abundance fetal variants. To address these limitations, we developed a highly sensitive and cost-effective analytical method utilizing high-resolution tandem mass spectrometry, capable of accurately detecting single nucleotide variants (SNVs) as early as 5-8 weeks gestation. It employs gas-phase enrichment combined with fragment mass spectral analysis for precise isolation and identification of fetal DNA amidst predominant maternal DNA. Analytical validation with synthetic DNA and cultured cells confirmed exceptional sensitivity, achieving single copy level detection despite significant interference. Clinically, our method accurately detected paternally inherited SNVs in 134 cell-free fetal DNA samples collected at 5-8 weeks gestation, achieving 100% accuracy. Additionally, it reliably identified pathogenic SNVs linked to phenylketonuria from 12 samples collected at 11-13 weeks gestation. This approach significantly reduces operational costs, enhances sensitivity, and eliminates false-negative results compared to traditional NGS-based methods.
科研通智能强力驱动
Strongly Powered by AbleSci AI