Department of Chemical Engineering, Brigham Young University, Provo, UT, USA.
Department of Chemical and Biomolecular Engineering, Ohio State University, Columbus, OH, USA.
Toxicol Appl Pharmacol. 2018 Apr 15;345:19-25. doi: 10.1016/j.taap.2018.02.016. Epub 2018 Feb 27.
Many diseases and disorders are linked to exposure to endocrine disrupting chemicals (EDCs) that mimic the function of natural estrogen hormones. Here we present a Rapid Adaptable Portable In-vitro Detection biosensor platform (RAPID) for detecting chemicals that interact with the human estrogen receptor β (hERβ). This biosensor consists of an allosteric fusion protein, which is expressed using cell-free protein synthesis technology and is directly assayed by a colorimetric response. The resultant biosensor successfully detected known EDCs of hERβ (BPA, E2, and DPN) at similar or better detection range than an analogous cell-based biosensor, but in a fraction of time. We also engineered cell-free protein synthesis reactions with RNAse inhibitors to increase production yields in the presence of human blood and urine. The RAPID biosensor successfully detects EDCs in these human samples in the presence of RNAse inhibitors. Engineered cell-free protein synthesis facilitates the use of protein biosensors in complex sample matrices without cumbersome protein purification.
许多疾病和失调都与接触到模拟天然雌激素功能的内分泌干扰化学物质(EDCs)有关。在这里,我们提出了一种用于检测与人类雌激素受体β(hERβ)相互作用的化学物质的快速适应便携式体外检测生物传感器平台(RAPID)。该生物传感器由别构融合蛋白组成,该蛋白使用无细胞蛋白合成技术表达,并通过比色反应直接进行测定。所得生物传感器成功地检测到已知的 hERβ 的 EDC(BPA、E2 和 DPN),其检测范围与类似的基于细胞的生物传感器相似或更好,但所需时间却大大缩短。我们还通过添加 RNA 酶抑制剂对无细胞蛋白合成反应进行了工程设计,以在存在人血和尿液的情况下提高产量。RAPID 生物传感器能够在存在 RNA 酶抑制剂的情况下成功检测出人血和尿液样本中的 EDC。经过工程设计的无细胞蛋白合成有助于在复杂的样本基质中使用蛋白质生物传感器,而无需繁琐的蛋白质纯化。