Twisted-Intramolecular-Charge-Transfer-Based Turn-On Fluorogenic
Nanoprobe for Real-Time Detection of Serum Albumin in Physiological
Conditions
Soham Samanta
Senjuti Halder
Gopal Das
10.1021/acs.analchem.8b01181.s001
https://acs.figshare.com/articles/journal_contribution/Twisted-Intramolecular-Charge-Transfer-Based_Turn-On_Fluorogenic_Nanoprobe_for_Real-Time_Detection_of_Serum_Albumin_in_Physiological_Conditions/6445556
Two cyanine-based fluorescent probes,
(<i>E</i>)-2-(4-(diethylamino)-2-hydroxystyryl)-3-ethyl-1,1-dimethyl-1<i>H</i>-benzo[<i>e</i>]indol-3-ium iodide (<b>L</b>) and (<i>E</i>)-3-ethyl-1,1-dimethyl-2-(4-nitrostyryl)-1<i>H</i>-benzo[<i>e</i>]indol-3-ium iodide (<b>L</b><sub><b>1</b></sub>), have been designed and synthesized. Of
these two probes, the twisted-intramolecular-charge-transfer (TICT)-based
probe, <b>L</b>, can preferentially self-assemble to form nanoaggregates. <b>L</b> displayed a selective turn-on fluorescence response toward
human and bovine serum albumin (HSA and BSA) in ∼100% aqueous
PBS medium, which is noticeable with the naked eye, whereas <b>L</b><sub><b>1</b></sub> failed to sense these albumin proteins.
The selective turn-on fluorescence response of <b>L</b> toward
HSA and BSA can be attributed to the selective binding of probe <b>L</b> with HSA and BSA without its interfering with known drug-binding
sites. The specific binding of <b>L</b> with HSA led to the
disassembly of the self-assembled nanoaggregates of <b>L</b>, which was corroborated by dynamic-light-scattering (DLS) and transmission-electron-microscopy
(TEM) analysis. Probe <b>L</b> has a limit of detection as low
as ∼6.5 nM. The sensing aptitude of probe <b>L</b> to
detect HSA in body fluid and an artificial-urine sample has been demonstrated.
2018-05-24 00:00:00
HSA
PBS
DLS
TICT
TEM
BSA
probe L
turn-on fluorescence response
Twisted-Intramolecular-Charge-Transfer-Based Turn-On Fluorogenic Nanoprobe