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Real-time measurement of Plasmodium falciparum-infected erythrocyte cytoadhesion with a quartz crystal microbalance

机译:石英晶体微量天平实时测量恶性疟原虫感染的红细胞粘附

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摘要

BackgroundAn important virulence mechanism of the malaria parasite Plasmodium falciparum is cytoadhesion, the binding of infected erythrocytes to endothelial cells in the second half of asexual blood stage development. Conventional methods to investigate adhesion of infected erythrocytes are mostly performed under static conditions, many are based on manual or semi-automated read-outs and are, therefore, difficult to standardize. Quartz crystal microbalances (QCM) are sensitive to nanogram-scale changes in mass and biomechanical properties and are increasingly used in biomedical research. Here, the ability of QCM is explored to measure binding of P. falciparum-infected erythrocytes to two receptors: CD36 and chondroitin sulfate A (CSA) under flow conditions.
机译:背景疟原虫恶性疟原虫的重要毒力机制是细胞粘附,即无性血液阶段发展的后半部分,受感染的红细胞与内皮细胞的结合。研究感染的红细胞粘附的常规方法通常在静态条件下进行,许多方法基于手动或半自动读数,因此难以标准化。石英晶体微天平(QCM)对质量和生物力学性能的纳克级变化敏感,并越来越多地用于生物医学研究中。在这里,探索了QCM在流动条件下测量恶性疟原虫感染的红细胞与两个受体(CD36和硫酸软骨素A(CSA))结合的能力。

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