The origin of the excitation wavelength (λex)-dependent photoluminescence (PL) of carbon dots (CDs) is poorly understood and still remains obscured. This phenomenon is often explained on the basis of surface trap/defect states, while the effect of quantum confinement is highly neglected in the literature. Here, we have shown that the λex-dependent PL of CDs is mainly due to the inhomogeneous size distribution. We have demonstrated the λex-dependent PL quenching of CDs inside the ferritin nanocages through selective optical excitation of differently sized CDs. It has been observed that Fe(3+) ions of ferritin effectively quench the PL of CDs due to static electron transfer, which is driven by favorable electrostatic interactions. However, control experiment with aqueous Fe(3+) ions in bulk medium revealed λex-independent PL quenching of CDs. The λex-dependent PL quenching of CDs by Fe(3+) ions of ferritin has been rationalized on the basis of a different extent of accessibility of Fe(3+) ions by differently sized CDs through the funnel-shaped ferritin channels. PL microscopy of individual CDs has been performed to get further information about their inherent PL properties at single dot resolution. Our results have shown that these hydrophilic CDs can be used as potential iron sensors in biological macromolecules.

The molecular origin behind the concentration-dependent intrinsic blue fluorescence of human serum albumin (HSA) is not known yet. This unusual blue fluorescence is believed to be a characteristic feature of amyloid-like fibrils of protein/peptide and originates due to the delocalization of peptide bond electrons through the extended hydrogen bond networks of cross-β-sheet structure. Herein, by combining the results of spectroscopy, size exclusion chromatography, native gel electrophoresis, and confocal microscopy, we have shown that the intrinsic blue fluorescence of HSA exclusively originates from oligomeric interfaces devoid of any amyloid-like fibrillar structure. Our study suggests that this low energy fluorescence band is not due to any particular residue/sequence, but rather it is a common feature of self-assembled peptide bonds. The present findings of intrinsic blue fluorescence from oligomeric interfaces pave the way for future applications of this unique visual phenomenon for early stage detection of various protein aggregation related human diseases.

Proteins inside a cell remain in highly crowded environments, and this often affects their structure and activity. However, most of the earlier studies involving serum albumins were performed under dilute conditions, which lack biological relevance. The effect of protein-protein interactions on the structure and properties of serum albumins at physiological conditions have not yet been explored. Here, we report for the first time the effect of protein-protein and protein-crowder interactions on the structure and stability of two homologous serum albumins, namely, human serum albumin (HSA) and bovine serum albumin (BSA), at physiological conditions by using spectroscopic techniques and scanning electron microscopy (SEM). Concentration-dependent self-oligomerization and subsequent structural alteration of serum albumins have been explored by means of fluorescence and circular dichroism spectroscopy at pH 7.4. The excitation wavelength (λex) dependence of the intrinsic fluorescence and the corresponding excitation spectra at each emission wavelength indicate the presence of various ground state oligomers of serum albumins in the concentration range 10-150 μM. Circular dichroism and thioflavin T binding assay revealed formation of intermolecular β-sheet rich interfaces at high protein concentration. Excellent correlations have been observed between β-sheet content of both the albumins and fluorescence enhancement of ThT with protein concentrations. SEM images at a concentration of 150 μM revealed large dispersed self-oligomeric states with sizes vary from 330 to 924 nm and 260 to 520 nm for BSA and HSA, respectively. The self-oligomerization of serum albumins is found to be a reversible process; upon dilution, these oligomers dissociate into a native monomeric state. It has also been observed that synthetic macromolecular crowder polyethylene glycol (PEG 200) stabilizes the self-associated state of both the albumins which is contrary to expectations that the macromolecular crowding favors compact native state of proteins.

In the present study, we have demonstrated the excitation energy transfer (EET) from silicon quantum dots (Si QDs) to silver nanoparticles (Ag NPs) and its modulation in the presence of cetyltrimethylammonium bromide (CTAB) surfactant by means of steady-state and time-resolved photoluminescence (PL) spectroscopy. Significant spectral overlap between the emission spectrum of Si QDs and localized surface plasmon resonance of Ag NPs results in a substantial amount of PL quenching of Si QDs. In addition, the PL lifetime of Si QDs is shortened in the presence of Ag NPs. The origin of this PL quenching has been rationalized on the basis of increased nonradiative decay rate due to excitation energy transfer from Si QDs to Ag NPs surface. The observed energy-transfer efficiency correlates well with the nanometal surface energy transfer theory with a 1/d 4 distance dependence rather than conventional Forster resonance energy transfer theory. It has also been observed that the EET efficiency drastically reduces in the presence of 0.5 mM CTAB. Dynamic light scattering and single-particle PL microscopy results indicate the formation of large surfactant-induced aggregates of Ag NPs. Finally, the energy-transfer efficiency values obtained from experiment have been used to calculate the distance between Si QDs and Ag NPs in the absence and presence of CTAB, which correlates well with the proposed model.

With the advent of newer luminescent nanoparticles for bioimaging applications, their complex interactions with individual biomolecules need to be understood in great detail, before their direct application into cellular environments. Here, we have presented a systematic and detailed study on the interaction between luminescent polymer nanodots (PNDs) and human serum albumin (HSA) in its free and ligand-bound state with the help of spectrophotometric and calorimetric techniques. At physiological pH (pH = 7.4), PNDs quench the intrinsic fluorescence of HSA as a consequence of ground-state complex formation. The binding stoichiometry and various thermodynamic parameters have been evaluated by using isothermal titration calorimetry and the van't Hoff equation. It has been found that the association of PNDs with HSA is spontaneous (ΔG = -32.48 ± 1.24 kJ mol) and is driven by a favorable negative standard enthalpy change (ΔH = -52.86 ± 2.12 kJ mol) and an unfavorable negative standard entropy change (ΔS = -68.38 ± 2.96 J mol K). These results have been explained by considering hydrogen bonding interactions between amino and hydroxyl groups (-NH and -OH) of PNDs and carboxylate groups (-COO) of glutamate (Glu) and aspartate (Asp) residues of HSA. The binding constant of PNDs with HSA is estimated to be 4.90 ± 0.19 × 10 M. Moreover, it has been observed that warfarin-bound HSA (war-HSA) shows a significantly lower binding affinity (K = 1.15 ± 0.19 × 10 M) toward PNDs, whereas ibuprofen-bound HSA (ibu-HSA) shows a slightly lower affinity (K = 3.47 ± 0.13 × 10 M) compared with the free HSA. In addition, our results revealed that PNDs displace warfarin from site I (subdomain IIA) of HSA because of the partial unfolding of war-HSA. We hope that the present study will be helpful to understand the fundamental interactions of these biocompatible PNDs with various biological macromolecules.

Here, we report the microscopic evidence of "necklace and bead"-like morphology, which has long been the most widely accepted model for polymer-surfactant complexes. The lack of microscopic evidence of the initial complexation between surfactant and polymer has resulted in many contradictory reports in the literature. In this paper, we visualized these initial complexes formed between negatively charged surfactant sodium dodecyl sulfate (SDS) with neutral poly(vinylpyrrolidone) (PVP) and cationic poly(diallyldimethylammonium chloride) (PDADMAC) polymer through photoluminescence (PL) microscopy and atomic force microscopy (AFM) using silicon quantum dot (Si QD) as an external PL marker. It is observed that, for the PVP-SDS system, SDS molecules bind at the hydrophobic sites on the random-coiled PVP chain through their hydrocarbon tails, while for the PDADMAC-SDS system, SDS head groups are associated with the positively charged nitrogen centers of the polymer, where the polymer chain wraps around the surfactant head groups.

Iron is a key nutrient as well as a potential toxin for almost all living organisms. In mammalian cells, serum transferrin (Tf) is responsible for iron transport and its iron overload/deficiency causes various diseases. Therefore, closely regulated iron homeostasis is extremely essential for cellular metabolism. In the present article we report the pH-dependent luminescence turn-on/off sensing of bound Fe(3+) ions of serum Tf by carbon dots (CDs) with the help of photoluminescence (PL) spectroscopy, FTIR spectroscopy, dynamic light scattering (DLS), circular dichroism (CD) and PL imaging techniques. At physiological pH (7.4), the intrinsic luminescence of CDs gets quenched in the presence of Tf as a consequence of ground-state association, which is driven by favorable electrostatic interactions between negatively charged CDs (-25.45 ± 1.23 mV) and positively charged Fe(3+) ions of Tf. The estimated detection limit of Tf by CDs at physiological pH is found to be 1.82 μM (signal-to-noise ratio of 3), which is much lower than the in vivo plasma concentration of Tf (∼ 25-35 μM). Various thermodynamic parameters have been evaluated by using the van't Hoff equation. Importantly, the secondary structure of Tf remains unaltered upon association with CDs. However, at pH 3.5, no such luminescence quenching of CDs has been observed in the presence of Tf due to the lack of ground-state interactions between positively charged (+17.63 ± 0.84 mV) CDs and Tf. Furthermore, the results from UV-Vis and far-UV CD measurements revealed a significant conformational change of Tf at pH 3.5 relative to pH 7.4, which triggers the subsequent release of bound iron from Tf. PL microscopy of individual CD revealed significant luminescence quenching at the single particle level, which further supports the non-emissive ground-state complexation at pH 7.4. Our present results show that these chemically synthesized water-dispersed CDs have the ability to selectively sense the bound iron from released iron of Tf without any conformational perturbation and hence they can be used as potential biological iron sensors as well as luminescent markers for the detection of iron deficiency/overload in biological macromolecules.

Graphene/Ferromagnet hybrid heterostructure is an important building block of spintronics due to unique ability of graphene to transport spin current over unprecedented distance and possible increase in its spin-orbit coupling...