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高通量均相检测李斯特菌属 DNA 的方法。

High-throughput homogenous assay for the direct detection of Listeria monocytogenes DNA.

机构信息

United States Department of Agriculture, Agricultural Research Service, Eastern Regional Research Center, 600 East Mermaid Ln., Wyndmoor, PA, 19038, USA.

出版信息

Sci Rep. 2024 Mar 25;14(1):7026. doi: 10.1038/s41598-024-56911-8.

Abstract

The Amplified Luminescent Proximity Homogenous Assay-linked Immunosorbent Assay (AlphaLISA) is known for detecting various protein targets; however, its ability to detect nucleic acid sequences is not well established. Here, the capabilities of the AlphaLISA technology were expanded to include direct detection of DNA (aka: oligo-Alpha) and was applied to the detection of Listeria monocytogenes. Parameters were defined that allowed the newly developed oligo-Alpha to differentiate L. monocytogenes from other Listeria species through the use of only a single nucleotide polymorphism within the 16S rDNA region. Investigations into the applicability of this assay with different matrices demonstrated its utility in both milk and juice. One remarkable feature of the oligo-Alpha is that greater sensitivity could be achieved through the use of multiple acceptor oligos compared to only a single acceptor oligo, even when only a single donor oligo was employed. Additional acceptor oligos were easily incorporated into the assay and a tenfold change in the detection limit was readily achieved, with detection limits of 250 attomole of target being recorded. In summary, replacement of antibodies with oligonucleotides allows us to take advantage of genotypic difference(s), which both expands its repertoire of biological markers and furthers its use as a diagnostic tool.

摘要

被扩增发光邻近均相免疫分析(AlphaLISA)以检测各种蛋白质靶标而闻名;然而,其检测核酸序列的能力尚未得到很好的证实。在这里,AlphaLISA 技术的功能得到扩展,包括直接检测 DNA(又名寡聚 Alpha),并应用于检测单核细胞增生李斯特菌。通过在 16S rDNA 区域内仅使用单个核苷酸多态性,定义了参数,使新开发的寡聚 Alpha 能够通过使用仅在 16S rDNA 区域内的单个核苷酸多态性来区分单核细胞增生李斯特菌和其他李斯特菌物种。对不同基质中该检测方法适用性的研究表明,它在牛奶和果汁中都具有实用性。寡聚 Alpha 的一个显著特点是,与仅使用单个受体寡聚体相比,通过使用多个受体寡聚体可以实现更高的灵敏度,即使仅使用单个供体寡聚体也是如此。可以轻松地将其他受体寡聚体纳入该检测方法中,检测限可轻易地提高十倍,检测限达到 250 飞摩尔的目标。总之,用寡核苷酸取代抗体可以使我们利用基因型差异,这不仅扩展了其生物标志物的范围,而且进一步将其用作诊断工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db0/10963731/f3e132de58a2/41598_2024_56911_Fig1_HTML.jpg

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