Detection of single-base mutation of DNA oligonucleotides with different lengths by terahertz attenuated total reflection microfluidic cell.
Mingjie TangMingkun ZhangLiangping XiaZhongbo YangShihan YanHuabin WangDongshan WeiChunlei DuHong-Liang CuiPublished in: Biomedical optics express (2020)
Many human genetic diseases are caused by single-base mutation in the gene sequence. Since DNA molecules with single-base mutation are extremely difficult to differentiate, existing detection methods are invariably complex and time-consuming. We propose a new label-free and fast terahertz (THz) spectroscopic technique based on a home-made terahertz attenuated total reflection (ATR) microfluidic cell and a terahertz time-domain spectroscopy (THz-TDS) system to detect single-base-mutated DNA molecules. The detected object DNA molecules are normal hemoglobin gene, sickle cell anemia gene (15 nt), JAK2 gene wild type and JAK2 V617F gene mutation (39 nt) from sickle cell anemia and thrombocytopenia, respectively. Results show that the oligonucleotide fragments with single-base mutation can be identified by THz spectroscopy combined with the ATR microfluidic cell, and the recognition effect of short oligonucleotide fragments with single-base mutation is better than that of long oligonucleotide fragments. The terahertz biosensor is shown to have high sensitivity and can be used to detect DNA molecules directly in the solution environment.
Keyphrases
- label free
- single cell
- single molecule
- circulating tumor
- cell free
- genome wide
- copy number
- circulating tumor cells
- high throughput
- chronic kidney disease
- healthcare
- wild type
- high resolution
- cell therapy
- genome wide identification
- stem cells
- mass spectrometry
- mesenchymal stem cells
- dna methylation
- working memory
- bone marrow
- transcription factor
- molecular dynamics simulations
- dna damage