Gillen Alice J, Kupis-Rozmysłowicz Justyna, Gigli Carlo, Schuergers Nils, Boghossian Ardemis A
École Polytechnique Fédérale de Lausanne (EPFL) , Lausanne 1015 , Switzerland.
Politecnico di Torino , Turin 10129 , Italy.
J Phys Chem Lett. 2018 Aug 2;9(15):4336-4343. doi: 10.1021/acs.jpclett.8b01879. Epub 2018 Jul 19.
The omnipresence of salts in biofluids creates a pervasive challenge in designing sensors suitable for in vivo applications. Fluctuations in ion concentrations have been shown to affect the sensitivity and selectivity of optical sensors based on single-walled carbon nanotubes wrapped with single-stranded DNA (ssDNA-SWCNTs). We herein observe fluorescence wavelength shifting for ssDNA-SWCNT-based optical sensors in the presence of divalent cations at concentrations above 3.5 mM. In contrast, no shifting was observed for concentrations up to 350 mM for sensors bioengineered with increased rigidity using xeno nucleic acids (XNAs). Transient fluorescence measurements reveal distinct optical transitions for ssDNA- and XNA-based wrappings during ion-induced conformation changes, with XNA-based sensors showing increased permanence in conformational and signal stability. This demonstration introduces synthetic biology as a complementary means for enhancing nanotube optoelectronic behavior, unlocking previously unexplored possibilities for developing nanobioengineered sensors with augmented capabilities.
生物流体中盐的普遍存在给设计适用于体内应用的传感器带来了普遍挑战。已表明离子浓度的波动会影响基于单链DNA包裹的单壁碳纳米管(ssDNA-SWCNTs)的光学传感器的灵敏度和选择性。我们在此观察到,当二价阳离子浓度高于3.5 mM时,基于ssDNA-SWCNT的光学传感器会出现荧光波长偏移。相比之下,对于使用异源核酸(XNA)进行生物工程改造以提高刚性的传感器,在浓度高达350 mM时未观察到偏移。瞬态荧光测量揭示了基于ssDNA和XNA的包裹在离子诱导的构象变化过程中不同的光学转变,基于XNA的传感器在构象和信号稳定性方面表现出更高的持久性。这一证明引入了合成生物学作为增强纳米管光电行为的补充手段,为开发具有增强功能的纳米生物工程传感器开辟了以前未探索的可能性。