Department of Chemistry, Paderborn University, Warburgerstraße 100, D-33098 Paderborn, Germany.
State Key Laboratory of Chemical Resource Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beisuanhuandonglu N.15, 100029 Beijing, China.
ACS Appl Mater Interfaces. 2020 Aug 19;12(33):36873-36881. doi: 10.1021/acsami.0c08722. Epub 2020 Aug 6.
Lysophosphatidic acid (LPA) as the biomarker of early stage ovarian cancer is essentially difficult to detect due to lack of target spots. A dually crosslinked supramolecular hydrogel (DCSH) was developed to achieve sensing of LPA, which acts as a competitive guest molecule triggering the responsive crosslinking of the DCSH. Through this strategy, the surface plasmon resonance combined with optical waveguide spectroscopy could be used to quantitatively detect LPA with a responsive range covering physiological conditions (in pure form as well as mimicking LPA plasma solution) with high selectivity and sensitivity. LPA efficiently immerses into the host molecule β-cyclodextrin (β-CD) up to a 1:2 ratio by the competitive interaction mechanism, confirmed by one-dimensional nuclear overhauser effect spectroscopy (1D NOESY), high-resolution mass spectrometry (HRMS), isothermal titration calorimetry (ITC), and computational simulation. Our method opens a new strategy to detect biomarkers without target spots and provides a platform for surface plasmon resonance (SPR)-based sensors measuring small molecules.
溶血磷脂酸(LPA)作为早期卵巢癌的生物标志物,由于缺乏靶标,因此本质上难以检测。本研究开发了一种双重交联超分子水凝胶(DCSH),以实现对 LPA 的传感,LPA 作为一种竞争性客体分子触发 DCSH 的响应性交联。通过该策略,表面等离子体共振与光波导光谱学相结合,可用于定量检测 LPA,响应范围涵盖生理条件(纯形式以及模拟 LPA 血浆溶液),具有高选择性和灵敏度。通过竞争相互作用机制,LPA 有效地将自身插入到主体分子β-环糊精(β-CD)中,比例高达 1:2,这一点通过一维核磁共振(1D NOESY)、高分辨率质谱(HRMS)、等温热力学滴定(ITC)和计算模拟得到了证实。我们的方法为检测无靶标生物标志物开辟了一条新策略,并为基于表面等离子体共振(SPR)的小分子传感器提供了一个平台。