Shrestha Anura, Lim Butaek, Shiveshwarkar Priyanka, Rojas Gumaro, Abure Izele, Nelson Anthony David, Jaworski Justyn
Department of Bioengineering, University of Texas at Arlington, Arlington, Texas, 76010, U.S.A.
Macromol Res. 2021 Sep;29(9):577-581. doi: 10.1007/s13233-021-9079-3. Epub 2021 Sep 25.
The use of polydiacetylene (PDA) vesicles in sensing systems are wide-spread due to the interesting optical properties of this stimuli-responsive material; however, agglutination based sensing with PDA have been relatively underutilized. To demonstrate the means for rapidly generating an agglutination probe based on peptide-displaying polydiacetylene vesicles, we implement here the use of a biotin mimetic peptide functionalized to a diacetylene amphiphile for proof-of-concept detection of a multivalent target, specifically streptavidin. Tuning of the vesicle composition revealed a distinct limit in the surface density of peptide amphiphile that could be displayed for this particular peptide sequence. A wide operational detection range was demonstrated, and the result also revealed an effective agglutination response of the PDA-based probe to streptavidin suggesting possible use of future formulations in profiling other multivalent targets.
由于这种刺激响应材料具有有趣的光学特性,聚二乙炔(PDA)囊泡在传感系统中的应用十分广泛;然而,基于PDA的凝集传感相对未得到充分利用。为了证明基于展示肽的聚二乙炔囊泡快速生成凝集探针的方法,我们在此实现了将一种生物素模拟肽功能化到二乙炔两亲物上,用于多价靶标(特别是链霉亲和素)的概念验证检测。囊泡组成的调整揭示了针对该特定肽序列可展示的肽两亲物表面密度存在明显限制。展示了较宽的操作检测范围,结果还揭示了基于PDA的探针对链霉亲和素的有效凝集反应,表明未来配方可能用于分析其他多价靶标。