A rhodamine based turn-on chemosensor for Fe3+ in aqueous medium and interactions of its Fe3+ complex with HSA. (13th September 2017)

• Record Type: Journal Article
• Authors: Bhowmick, Rahul; Islam, Abu Saleh Musha; Giri, Arindam; Katarkar, Atul; Ali, Mahammad
• Is Part Of: New journal of chemistry. Volume 41:Number 20(2017)
• Page Start: 11661
• Page End: 11671
• Publication Date: 2017-09-13
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c7nj02446k
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : A novel hexa-coordinating rhodamine-based chemosensor, HL 6, selectively and rapidly recognizes Fe 3+ in the presence of a number of metal cations, numerous anions and amino acids in purely aqueous medium with live cell imaging applications. Abstract : A novel hexa-coordinating rhodamine-based chemosensor, HL 6, with N4 O2 donor atoms, selectively and rapidly recognizes Fe 3+ in the presence of all biologically relevant as well as toxic metal ions, numerous anions (except for F − and I −, which quench FI) and amino acids. The lower detection limit (110 nM) along with cytoplasmic cell imaging applications with negligible cytotoxicity provides a good opportunity towards in vitro / in vivo cell imaging of Fe 3+ ions. Scanning electron microscopy (SEM) studies reveal a spherical microstructure for the free ligand, HL 6, which melts upon increasing the applied voltage (≥2 kV); however, this is reduced in size in the presence of SDS, morphology remaining the same. [L 6 -Fe] 2+ gives hexagonal rod-like microstructures due to π⋯π stacking extended in a one dimensional fashion, which, in the presence of SDS, turn into cubic microstructures. However, in the presence of HSA both HL 6 and [L 6 -Fe] 2+ agglomerated severely. A plot of FI (or r ) vs. [SDS] at constant [L 6 -Fe 2+ ] (20 μM) shows a rapid decrease in FI (or r ); FI or r reaches a minimum at ∼2 mM SDS and then increases and becomes saturated at ≥8 mM SDS. The initial rapid decrease in FI or r with the increase in [SDS] arises due to the breakdown of the self-assembled microstructures of [L 6 -Fe] 2+ formed probably through π⋯π stacking in pure aqueous solution in the presence of SDS (≤2 mM). The increase in FI or r with [SDS] beyond 2 mM may arise due to trapping of the [L 6 -Fe] 2+ moiety inside the micellar cavity thereby giving it a thermodynamically rigid structure. Again, fluorescence anisotropy measured as a function of HSA concentration (0–70 μM) at a fixed concentration of HL 6 and Fe 3+ (20 μM each) at 555 nm showed a gradual increase in r with the increase in [HSA]. Site selective binding and molecular modeling studies revealed that [L 6 -Fe] 2+ predominantly binds in the subdomain IIA of HSA by both hydrophobic and electrostatic forces. A circular dichroism (CD) study clearly points towards the reduction in α-helical organization of the protein and subsequent increase in the coiled structure upon binding with [L 6 -Fe] 2+ indicating a small but definitive partial unfolding of the protein.