Dielectrophoresis spectroscopy for nucleotide identification in DNA

Md Fahim Shahriar , Janisa Kabir , Ding Piaopiao
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Abstract

DNA sequence with a known physical position on a chromosome is called a genetic marker, so the causal gene may identify with genetic markers in different kinds of hereditary diseases. DNA segments near one another on a chromosome often inherit the other concurrently; as a result, the inheritance of a neighboring gene that has not yet been discovered but whose general position is tracked by using genetic markers. So, Genetic markers can play a significant role in biological research because they can contribute to identifying many diseases. Single nucleotide polymorphism, or SNP (pronounced “snip”), is the variation of a single nucleotide in a DNA due to genetic disorders. For example, in a specific region of DNA, an SNP may displace the nucleotide cytosine (C) with the nucleotide thymine (T). SNPs, or single nucleotide polymorphisms, are one of the most common genetic variations that assist in detecting many human diseases such as Migraine, Cancer, Schizophrenia, Sickle Cell Anemia, Alzheimer's Disease, etc. Hyperchromicity, Short Oligonucleotide Analysis Program (SOAP), quantitative PCR techniques, Fluorescence Polarization Melting Curve Analysis, SNP Microarrays, Intercalating Dyes, and many other techniques are commonly used to identify SNPs nowadays. However, those methods are not much reliable, a bit costly, time-consuming, and difficult to use, whereas dielectrophoresis can be an excellent way to detect SNP easily. A non-uniform electric field generated by electrodes interacts with polarizable suspended particles to regulate and alter particle movement; this process is known as dielectrophoresis (DEP). Cell transfer, in vitro fertilization, and biological testing are a few uses for dielectrophoresis, particularly in the biomedical industry. Cell fusion using dielectrophoresis has also improved crossbreeding, cancer treatment, and scientific research. Most notably, dielectrophoresis is used to classify changes in the electrical characteristics of cells. In this phenomenon, when a dielectric particle is exposed to a non-uniform electric field, a force is produced on it, and this DEP force may be utilized to recognize the variations in a single location in a DNA sequence. DEP is less time-consuming, cheap, and reliable than other processes to detect SNPs easily.

用于DNA核苷酸鉴定的双电泳光谱法
在染色体上具有已知物理位置的DNA序列称为遗传标记,因此致病基因可以在不同类型的遗传疾病中与遗传标记相识别。染色体上彼此靠近的DNA片段常常同时遗传另一个;结果,一个尚未被发现的邻近基因的遗传,但其一般位置是通过遗传标记来追踪的。因此,遗传标记可以在生物学研究中发挥重要作用,因为它们可以帮助识别许多疾病。单核苷酸多态性,或SNP(发音为“snip”),是由于遗传疾病导致的DNA中单个核苷酸的变异。例如,在DNA的特定区域,SNP可能用核苷酸胸腺嘧啶(T)取代核苷酸胞嘧啶(C)。SNP或单核苷酸多态性是最常见的遗传变异之一,有助于检测许多人类疾病,如偏头痛,癌症,精神分裂症,镰状细胞性贫血,阿尔茨海默病等。高染色、短寡核苷酸分析程序(SOAP)、定量PCR技术、荧光偏振熔化曲线分析、SNP微阵列、嵌入染料等许多目前常用的技术来鉴定SNP。然而,这些方法不太可靠,有点昂贵,耗时,并且难以使用,而介电电泳可以很容易地检测SNP。电极产生的非均匀电场与可极化悬浮粒子相互作用以调节和改变粒子运动;这个过程被称为介电电泳(DEP)。细胞移植、体外受精和生物测试是电泳术的一些用途,特别是在生物医学工业中。细胞融合使用电泳术也改善了杂交育种,癌症治疗和科学研究。最值得注意的是,电泳术被用来对细胞电特性的变化进行分类。在这种现象中,当介电粒子暴露在非均匀电场中时,会对其产生一个力,并且可以利用该DEP力来识别DNA序列中单个位置的变化。与其他检测snp的方法相比,DEP更省时、便宜、可靠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aspects of molecular medicine
Aspects of molecular medicine Molecular Biology, Molecular Medicine
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