an-integrated-system-to-remotely-trigger-intracellular-signal

An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation

Upconversion nanoparticle (UCNP)-mediated photoactivation is a new approach to remotely control bioeffectors with much less phototoxicity and with deeper ...

Academia Sinica

The rhenium-based rectangles [{Re(CO)(3)(mu-bpy)Br}{Re(CO)(3)(mu-L)Br}](2) (I, L = 4,4'-dipyridylacetylene (dpa); II, L = 4,4'-dipyridylbutadiyne (dpb); III, L = 1,4-bis(4'-pyridylethynyl)benzene (bpeb); bpy = 4,4'-bipyridine) are emissive in solution at room temperature. The presence of extended pi conjugation leads to an increase in electron delocalization, which, in turn, results in improved luminescence and lower nuclear reorganization energy. These rectangles, upon electronic excitation, undergo facile electron transfer (ET) reactions with quinones and both the dynamic and static quenching contribute to the reaction. Spectral and electrochemical measurements show that quinone 7,7,8,8-tetracyanoquinodimethane (TCNQ) binds strongly to rectangle I. The driving force dependence of k(et), deduced from the luminescence quenching of rectangles with quinones, can be well accounted for within the context of the Marcus theory of electron transfer.

Luminescence quenching of Re(I) molecular rectangles by quinones.

Organometallic calixarenes: syceelike tetrarhenium(I) cavitands with tunable size, color, functionality, and coin-slot complexation.

New concepts on the design and synthesis of crystalline metal-organic frameworks (MOFs) have made them a subject of considerable interest in the growing field of materials science. By creating larger cavity sizes by a nearly infinite combination of metal nodes and organic linkers, many innovative characteristics of microporous MOFs have been revealed. The primary goal of this perspective article is to highlight the frontiers in the development of giant MOFs that are deliberately constructed from metallated or metal-free bulky scaffolds. Incorporating these types of distinct bulky ligands into giant MOFs may lead to MOFs with a large cavity size, intriguing properties and new framework topology. Emerging applications of these materials in catalysis, adsorption, and sensors are also discussed.

Giant metal-organic frameworks with bulky scaffolds: from microporous to mesoporous functional materials.

Self-assembled metallacycles offer structural diversity and interesting properties based on their unique frameworks and host-guest chemistry. As a result, the design and synthesis of these materials has attracted significant research interest. This Account describes our comprehensive investigations of an effective orthogonal-bonding approach for the self-assembly of neutral Re-based metallacycles. We discuss the various types of assemblies that can be created based on the nuclearity of the luminophore, including bimetallic materials, rectangles, cages, and calixarenes. This approach permits the preparation of a rectangular molecule, rather than two molecular squares, in excellent yields. We extended this strategy to the high yield synthesis of a series of Re-based metallacycles with different shapes. With the rich spectroscopic and luminescence properties, Re(I) metallacycles provide an excellent platform for studies of host-guest interactions. When possible, we also present potential applications of the luminescent Re-based metallosupramolecular assemblies. The orthogonal-bonding approach involves the simultaneous introduction of two ligands: a bis-chelating ligand to coordinate to two equatorial sites of two fac-(CO)(3)Re cores and a monotopic or ditopic nitrogen-donor ligand to the remaining orthogonal axial site. Furthermore, by the appropriate choice of the predesigned organic ligands with various backbones and connectivity information and fac-Re(CO)(3) metal centers, we could also design other novel functional metallacycles including rotors, gondolas, cages, triangles, and metallacalixarenes in high yields. The incorporation of flexible ligands into the Re(I) metallacycles allows us to introduce various conformation states and novel structures. As a result, these structures acquire new functions, such as adaptive recognition properties. For example, we assembled Re(I)-based metallacyclic rotors via a one-step process. These rotors, which contain a para-phenylene unit that rapidly rotates within the metallacycles, are prototypes of a neutral altitudinal rotor. Most of the metallacycles are luminescent. The ability to chemically modify the organic ligands offers opportunities to create structural diversity and to tune the photophysical properties of these Re(I) metallacycles efficiently. Several strategies for increasing emission quantum yields and excited-state lifetimes and tuning the colors in Re(I) metallacycles are available. The cyclometalated ligands in Re(I) metallacycles improve excited state lifetimes and quantum yields, and these C-H bond-activated metallacycles are considerably more emissive than their non-C-H bond-activated analogues. The introduction of crown-ether-like recognition sites into neutral gondola-shaped metallacycles that selectively recognize metal ions also enhanced emission. Rhenium-based rectangular boxes, synthesized via a simple one-step route, contain a large and tunable hydrophobic inner cavity, which selectively recognizes benzene molecules. Such structures were the best host for benzene reported to date. In addition, we designed and synthesized novel neutral metallacalixarenes with tunable size, cavity, color, and functionality. These structures are efficient hosts for the recognition of planar aromatic guests.

One-step orthogonal-bonding approach to the self-assembly of neutral rhenium-based metallacycles: synthesis, structures, photophysics, and sensing applications.

The aggregation-induced emission enhancement (AIEE) characteristics of the two alkoxy-bridged binuclear Re(I) complexes [{Re(CO)3(1,4-NVP)}2(μ2-OR)2] (1, R = C4H9; 2, C10H21) bearing a long alkyl chain with 4-(1-naphthylvinyl)pyridine (1,4-NVP) ligand are illustrated. These complexes in CH2Cl2 (good solvent) are weakly luminescent, but their intensity increased enormously by almost 500 times by the addition of poor solvent (CH3CN) due to aggregation. By tracking this process via UV-vis absorption and emission spectral and TEM techniques, the enhanced emission is attributed to the formation of nanoaggregates. The nanoaggregate of complex 2 is used as a sensor for nitroaromatic compounds. Furthermore, the study of the photophysical properties of these binuclear Re(I) complexes in cationic, cetyltrimethylammonium bromide (CTAB), anionic, sodium dodecyl sulfate (SDS), and nonionic, p-tert-octylphenoxypolyoxyethanol (TritonX-100, TX-100), micelles as well as in CTAB-hexane-water and AOT-isooctane-water reverse micelles using steady-state and time-resolved spectroscopy and TEM analysis reveals that the nanoaggregates became small and compact size.

Aggregation-induced emission enhancement in alkoxy-bridged binuclear rhenium(I) complexes: application as sensor for explosives and interaction with microheterogeneous media.

Alkoxy bridged binuclear rhenium(I) complexes are used as a probe for the selective and sensitive detection of aggregation of β-amyloid fibrils that are consorted with Alzheimer's disease (AD). The strong binding of the complexes is affirmed by the fluorescence enhancement and calculated binding constant value in the order of 10(5)M(-1) is obtained from the Scatchard plots. The binding of β-amyloid can be attributed to π-π stacking interaction of naphthalene moiety present in rhenium(I) complexes, and it is supported by docking studies. The selectivity is quite high towards other proteins and the formation of fibrils can be observed in the range of 30-40 nm through the AFM and TEM techniques.

Alkoxy bridged binuclear rhenium (I) complexes as a potential sensor for β-amyloid aggregation.

Photoactivatable (caged) bioeffectors provide a way to remotely trigger or disable biochemical pathways in living organisms at a desired time and location with a pulse of light (uncaging), but the phototoxicity of ultraviolet (UV) often limits its application. In this study, we have demonstrated the near-infrared (NIR) photoactivatable enzyme platform using protein kinase A (PKA), an important enzyme in cell biology. We successfully photoactivated PKA using NIR to phosphorylate its substrate, and this induced a downstream cellular response in living cells with high spatiotemporal resolution. In addition, this system allows NIR to selectively activate the caged enzyme immobilized on the nanoparticle surface without activating other caged proteins in the cytosol. This NIR-responsive enzyme-nanoparticle system provides an innovative approach to remote-control proteins and enzymes, which can be used by researchers who need to avoid direct UV irradiation or use UV as a secondary channel to turn on a bioeffector.

Construction of a Near-Infrared-Activatable Enzyme Platform To Remotely Trigger Intracellular Signal Transduction Using an Upconversion Nanoparticle.

Rhenium nanoparticles (ReNPs) supported on ordered mesoporous carbon (OMC) as a catalyst (Re/OMC) through a solvent-evaporation induced self-assembly (ELSA) method were prepared. The synthesized heterogonous catalyst was fully characterized using X-ray diffraction, field emission transmission electron microscopy, N2 sorption, metal dispersion, thermogravimetric analysis, Raman, Fourier-transform infrared, and X-ray photon spectroscopies. In addition, the catalyst was applied to reduce the aromatic nitro compounds (ANCs) for the first time in aqueous media and the reactions were monitored by following the intensity changes in the UV-vis absorption spectra with respect to time. This method provides the advantages of obtaining a high rate constant (k), green reaction conditions, simple methodology, easy separation and easy workup procedures. Moreover, the catalyst can be easily recovered by centrifugation, recycled several times and reused without any loss of activity. The higher activity of this catalyst was attributed to higher dispersion and smaller particle size of ReNPs as observed from FE-TEM and XRD results.

Pounraj Thanasekaran

Institute of Chemistry

Academia Sinica

An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation

Pounraj Thanasekaran

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Institute of Chemistry

Academia Sinica

An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation

Institute of Chemistry