Park Soohyun, Gerber Alice, Santa Cátia, Aktug Gizem, Hengerer Bastian, Clark Heather A, Jonas Ulrich, Dostalek Jakub, Sergelen Khulan
BioMed X Institute, Heidelberg 69120, Germany.
Faculty of Biotechnology, Mannheim University of Applied Sciences, Mannheim 68163, Germany.
J Am Chem Soc. 2025 Apr 2;147(13):11485-11500. doi: 10.1021/jacs.5c01718. Epub 2025 Mar 20.
Continuous in vivo monitoring of small molecule biomarkers requires biosensors with reversibility, sensitivity in physiologically relevant ranges, and biological stability. Leveraging the real-time, label-free detection capability of surface plasmon resonance (SPR) technology, a molecularly responsive hydrogel film is introduced to enhance small molecule sensitivity. This advanced biosensing platform utilizes split-aptamer-cross-linked hydrogels (aptagels) engineered using 8-arm poly(ethylene glycol) macromers, capable of directly and reversibly detecting vancomycin. Investigation through SPR and optical waveguide mode, along with quartz crystal microbalance with dissipation (QCM-D) monitoring, reveals that the reversible formation of analyte-induced ternary molecular complexes leads to aptagel contraction and significant refractive index changes. Optimization of aptamer cross-link distribution and complementarity of split-aptamer pairs maximizes conformational changes of the aptagel, demonstrating a detection limit of 160-250 nM for vancomycin (6-9 fold improvement over monolayer counterpart) with a broad linear sensing range up to 1 mM. The aptagel maintains stability over 24 h in blood serum and 5 weeks in diluted blood plasma (mimicking interstitial fluid). This structurally responsive aptagel platform with superior stability and sensitivity offers promising avenues for continuous in vivo monitoring of small molecules.
对小分子生物标志物进行连续的体内监测需要具有可逆性、在生理相关范围内具有灵敏度以及生物稳定性的生物传感器。利用表面等离子体共振(SPR)技术的实时、无标记检测能力,引入了一种分子响应水凝胶膜以提高小分子灵敏度。这种先进的生物传感平台利用了使用八臂聚乙二醇大分子单体设计的分裂适体交联水凝胶(aptagels),能够直接且可逆地检测万古霉素。通过SPR和光波导模式以及带有耗散的石英晶体微天平(QCM-D)监测进行的研究表明,分析物诱导的三元分子复合物的可逆形成导致aptagel收缩和显著的折射率变化。适体交联分布的优化和分裂适体对的互补性使aptagel的构象变化最大化,显示出对万古霉素的检测限为160 - 250 nM(比单层对应物提高了6 - 9倍),线性传感范围宽至1 mM。aptagel在血清中24小时内以及在稀释血浆(模拟组织间液)中5周内均保持稳定。这种具有卓越稳定性和灵敏度的结构响应性aptagel平台为小分子的连续体内监测提供了有前景的途径。