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用于流式细胞术蛋白质定量的磁功能化微丝的微流体集成

Microfluidic Integration of Magnetically Functionalized Microwires for Flow Cytometry Protein Quantification.

作者信息

Clime Liviu, Pavel Catalin, Malic Lidija, Nassif Christina, Geissler Matthias, Lupu Nicoleta, Óvári Tibor-Adrian, Poncelet Lucas, Veilleux Gaétan, Moslemi Elham, Hernández-Castro Javier Alejandro, Sinnett Daniel, Che Diping, Veres Teodor

机构信息

Life Sciences Division, National Research Council of Canada, 75 de Mortagne Boulevard, Boucherville, QC J4B 6Y4, Canada.

Azure Biosystems, 4810 Jean Talon O., Suite 328, Montreal, QC H4P 2N5, Canada.

出版信息

Materials (Basel). 2025 Jan 7;18(2):215. doi: 10.3390/ma18020215.

Abstract

A novel approach to protein quantification utilizing a microfluidic platform activated by a magnetic assembly of functionalized magnetic beads around soft magnetic capture centers is presented. Functionalized magnetic beads, known for their high surface area and facile manipulation under external magnetic fields, are injected inside microfluidic channels and immobilized magnetically on the surface of glass-coated soft magnetic microwires placed along the symmetry axis of these channels. A fluorescent (Cy5) immunomagnetic sandwich ELISA is then performed by sequentially flowing the sample and all necessary reagents in the microfluidic channels. Direct protein quantification is performed by magnetically releasing the beads from the microwire and evaluating their fluorescence intensity with the help of a miniature (microfluidic-based) flow cytometer. Measurements of ICAM-1 protein concentration in human blood plasma samples confirm the feasibility of the approach through extensive performance benchmarking. The automation and multiplexing capabilities of the proposed platform further demonstrate its potential for protein quantification in point-of-care settings using microfluidics and miniature flow cytometry instruments.

摘要

本文提出了一种利用微流控平台进行蛋白质定量的新方法,该平台由围绕软磁捕获中心的功能化磁珠的磁性组件激活。功能化磁珠以其高表面积和在外部磁场下易于操作而闻名,被注入微流控通道内,并通过磁场固定在沿这些通道对称轴放置的玻璃涂层软磁微丝表面。然后,通过在微流控通道中依次流动样品和所有必要试剂,进行荧光(Cy5)免疫磁夹心ELISA。通过从微丝上磁性释放珠子,并借助微型(基于微流控的)流式细胞仪评估其荧光强度,来进行直接蛋白质定量。通过广泛的性能基准测试,对人血浆样品中ICAM-1蛋白浓度的测量证实了该方法的可行性。所提出平台的自动化和多重检测能力进一步证明了其在使用微流控和微型流式细胞仪的即时检测环境中进行蛋白质定量的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c46/11766812/eaf3219b8524/materials-18-00215-g001.jpg

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