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Quantum Dot Labelling of Tepary Bean (Phaseolus acutifolius) Lectins by Microfluidics

机译:微流控技术对三元豆凝集素的量子点标记

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摘要

Lectins are bioactive proteins with the ability to recognize cell membrane carbohydrates in a specific way. Diverse plant lectins have shown diagnostic and therapeutic potential against cancer, and their cytotoxicity against transformed cells is mediated through the induction of apoptosis. Previous works have determined the cytotoxic activity of a Tepary bean ( ) lectin fraction (TBLF) and its anti-tumorigenic effect on colon cancer. In this work, lectins from the TBLF were additionally purified by ionic-exchange chromatography. Two peaks with agglutination activity were obtained: one of them was named TBL-IE2 and showed a single protein band in two-dimensional electrophoresis; this one was thus selected for coupling to quantum dot (QD) nanoparticles by microfluidics (TBL-IE2-QD). The microfluidic method led to low sample usage, and resulted in homogeneous complexes, whose visualization was achieved using multiphoton and transmission electron microscopy. The average particle size (380 nm) and the average zeta potential (−18.51 mV) were determined. The cytotoxicity of the TBL-IE2 and TBL-IE2-QD was assayed on HT-29 colon cancer cells, showing no differences between them ( ≤ 0.05), where the LC values were 1.0 × 10 and 1.7 × 10 mg/mL, respectively. The microfluidic technique allowed control of the coupling between the QD and the protein, substantially improving the labelling process, providing a rapid and efficient method that enabled the traceability of lectins. Future studies will focus on the potential use of the QD-labelled lectin to recognize tumor tissues.
机译:凝集素是生物活性蛋白,具有以特定方式识别细胞膜碳水化合物的能力。多种植物凝集素已显示出对癌症的诊断和治疗潜力,并且它们对转化细胞的细胞毒性是通过诱导凋亡来介导的。以前的工作已经确定了三元豆()凝集素级分(TBLF)的细胞毒性活性及其对结肠癌的抗肿瘤发生作用。在这项工作中,来自TBLF的凝集素还通过离子交换色谱法进行了纯化。获得了两个具有凝集活性的峰:其中一个峰名为TBL-IE2,在二维电泳中​​显示单个蛋白条带。因此,通过微流控技术(TBL-IE2-QD)选择了一种与量子点(QD)纳米粒子偶联的化合物。微流控方法导致样品使用率低,并导致均相的络合物,使用多光子和透射电子显微镜可以实现其可视化。测定平均粒径(380nm)和平均ζ电势(-18.51mV)。在HT-29结肠癌细胞上测定了TBL-IE2和TBL-IE2-QD的细胞毒性,显示它们之间没有差异(≤0.05),其中LC值分别为1.0×10和1.7×10 mg / mL。 。微流体技术可以控制QD与蛋白质之间的偶联,从而显着改善标记过程,提供了一种快速有效的方法,可实现凝集素的可追溯性。未来的研究将集中于使用QD标记的凝集素识别肿瘤组织的潜在用途。

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