Cell Staining by Photo-activated Dye and Its Conjugate with Chitosan.

Photo-activated or "Caged" rhodamine dyes are the most useful for microscopic investigation of biological tissue by various fluorescent techniques. Novel precursor of the fluorescent dye (PFD813) has been studied for photosensitive staining of numerous animal cells. The functional rhodamine dye (Rho813) with intensive fluorescence has been obtained after photoactivation of its precursor PFD813 inside cells. The dye Rho813 has been successfully used for the optical detection of particular features in biological objects (HaCaT cells, HBL-100, MDCK, lymphocytes). Moreover, the chitosan conjugate with PFD molecules ("Chitosan-PFD813″) has been obtained and studied for the first time. The developed procedures and obtained data are important for further applications of novel precursors of fluorescent dyes ("caged" dyes) for microscopic probing of biological objects. As example, the synthesized "Chitosan-PFD813″ has been successfully applied in this study for intracellular transport visualization by fluorescent microscopy.

Novel precursors of fluorescent dyes. 1. Interaction of the dyes with model phospholipid in monolayers.

Photoactivated ("caged") fluorescent dyes are modern tools for structure and function studies of cell membranes and subcellular organelles. Recently synthesized precursors of rhodamine fluorescent dyes (abbreviations PFD813 and PFD814) important for microscopic probing of biological objects have been studied in solution. In order to characterize the behavior at interfaces, monolayers of PFD813 and PFD814 on water have been formed and investigated. The interactions of these precursors with the biomembrane component dimyristoylphosphatidylethanolamine in monolayers at the air-water interface and after transfer to glass plates have been studied by measuring monolayer parameters and spectroscopic properties before and after photo-chemical formation of the fluorescent rhodamine dyes Rho813 and Rho814, respectively.

Optical characterization of asphaltenes at the air-water interface.

Asphaltenes extracted from Arabian light crude oil have been investigated at the air-water interface of a Langmuir trough by in situ optical techniques. Brewster angle microscopy (BAM) and reflection spectroscopy have been used to extract new information about the microscopic organization of the asphaltene films in terms of association phenomena and chromophore orientation, respectively. The use of different spreading concentrations in the range 0.1-15 mg mL-1 reveals significant changes in the behavior at the interface with more condensed isotherms above 2 mg mL-1. This break point is related to the nanoaggregate-to-cluster association threshold in organic solution widely accepted in the recent asphaltene literature. BAM images support this observation with very different morphologies for the two spreading concentrations employed, 0.1 and 4 mg mL-1, respectively. The study of intensity changes in the corresponding normalized reflection spectra also confirms the transition in the asphaltene interfacial behavior between these two spreading concentrations. Finally, this technique helps with understanding the changes observed in the asphaltene films during a set of compression-decompression cycles.

Influence of monolayer state on spectroscopy and photoisomerization of an amphiphilic styryl-pyridinium dye on a solid substrate.

The spectroscopy and photochromic properties of transferred monolayers of the amphiphilic styryl-pyridinium dye 4-(3',4'-dimethoxystyryl)-N-octadecylpyridinium perchlorate (DMPOP) were studied at different conditions during their transfer. The emission maxima of the monolayers transferred from the air-water interface in the liquid-expanded phase are strongly dependent on the surface pressure applied during the transfer process, even at values when the area per molecule is 2-3 times larger than the area occupied by a chromophore. In monolayers transferred from the liquid-condensed phase, the presence of a different kind of aggregates was observed. The fluorescence emission properties of the monolayers can be reversibly modulated by photoinduced E-Z isomerization. A blue shift up to 72 nm in the emission maximum, depending on the transfer conditions of the films, can be obtained by irradiation with blue light, and partially recovered (a red shift of up to 26 nm) with UV radiation. The rate at which the first process (E-->Z) takes place is drastically reduced in monolayers transferred from the liquid-condensed phase as compared to those transferred from the liquid-expanded one. However, the rate of the reverse reaction (Z-->E) is not significantly altered. These properties make DMPOP a promising material for the preparation of Langmuir-Blodgett films, whose properties can be effectively controlled by the transfer conditions and subsequently optically modulated, for potential applications as photonics devices for data storage.

Imaging of the domain organization in sphingomyelin and phosphatidylcholine monolayers.

The lateral organization of biomembranes has gained significant interest when the fluid mosaic model was challenged by the model of "lipid rafts". Several lipid classes like cholesterol and sphingolipids are considered to be essential for their formation. Here we investigate the lateral domain formation in binary mixtures of sphingomyelin and phosphatidylcholine. Both are major lipid components of lipoproteins and mammalian cell membranes at various molar ratios. Surface pressure-area isotherms and surface potential-area isotherms of monolayers composed of these lipids clearly indicated non-ideal mixing. In addition, Brewster angle microscopy provided a well-suited approach to image the formation of lateral domains. These images demonstrated that pure sphingomyelin forms very stable finger-like domains that exhibit a distinct internal organization suggesting an anisotropic orientation of the acyl side chains. Similar behavior was found for mixtures containing more than 60 mol% sphingomyelin. With increasing content of phosphatidylcholine the domain size decreased and the surface pressure, where domain formation occurred, increased. At lower sphingomyelin content (30-60 mol%) rather round-shaped, smaller domains were observed. Thus, the potential of sphingomyelin domains as potentially important building blocks for actual domains that could be building blocks for raft formation is suggested, even without the presence of cholesterol. In addition, these observations may suggest a role for the distinct molar ratio of these key lipids frequently found in physiologically relevant particles such as low and high density lipoproteins or the outer leaflet of the human erythrocyte membrane.

Use of UV-vis reflection spectroscopy for determining the organization of viologen and viologen tetracyanoquinodimethanide monolayers.

UV-vis reflection spectroscopy has been used for proving in situ the organization of pure viologen and hybrid viologen tetracyanoquinodimethanide monolayers at the air-water interface. Other more classical measurements concerning Langmuir monolayers, including surface pressure-area and surface potential-area isotherms, are also provided. The organization of the viologen in the Langmuir monolayer was investigated upon the different states of compression, and the tilt angle of the viologen moieties with respect to the water surface was determined. A gradual transition of the viologen molecules from a flat orientation in the gas phase to a more tilted position with respect to the water surface in the condensed phases occurs. The addition of a tetracyanoquinodimethane (TCNQ) salt in the subphase leads to the penetration of TCNQ anions into the positively charged viologen monolayer forming a hybrid viologen tetracyanoquinodimethanide film where a charge-transfer interaction between the two moieties is observed. From a quantitative analysis of the reflection spectra, an organization model of these hybrid monolayers at the air-water interface is proposed, suggesting a parallel arrangement of viologen and TCNQ units with a 1:2 stoichiometry.

Molecular organization of an amphiphilic styryl pyridinium dye in monolayers at the air/water interface in the presence of various anions.

Amphiphilic 4-(3',4'-dimethoxystyryl)-N-octadecylpyridinium perchlorate and bromide form stable monolayers at the air/water interface. Small differences in the surface pressure-area and surface potential-area isotherms depending on the anion indicate interactions between the chromophore and the anions on the pure water subphase. The monolayer behavior is considerably modified on 10 mM aqueous solutions of KI, KClO4, KCl, and KF as revealed by isotherm measurements, reflection spectroscopy, and Brewster angle microscopy. The phase transition observed in the isotherms is shifted to higher surface pressure because of variation of the salt according to the Hofmeister series. Upon monolayer compression, the chromophores are increasingly tilted, and a shift of the band to longer wavelengths is attributed to the environment becoming less polar. However, in the case of KCl at small areas per molecule, relaxation is observed at constant area with the appearance of a new band shifted to shorter wavelengths. This band is assigned to small associates of about four chromophores (H aggregates). In the case of KI, a new band shifted to longer wavelengths is found. Theoretical calculations did not yield a transition in the observed range, even for large aggregates (J aggregates). Therefore, other interactions may be responsible for the appearance of this band.