Photoelectron microscopy and photoelectron quantum yields of the fluorescent dyes fluorescein and rhodamine.

Photoelectric properties of the dyes fluorescein and rhodamine were determined with the aim of assessing the usefulness of these compounds as labels in photoelectron microscopy. The photoelectron quantum yields were measured over the wavelength range 180-230 nm. At 230 nm the quantum yields for fluorescein disodium salt, rhodamine B free base and rhodamine B HCl salt are approximately 10(-5) electrons per incident photon. At 180 nm these values rise to approximately 10(-3) electrons per incident photon. All forms of fluorescein do not have the same quantum yield. The neutral form of fluorescein has a quantum yield an order of magnitude lower than the disodium salt. Beam current measurements were performed on labeled and unlabeled proteins to determine the effect of the high light intensity employed in the photoelectron microscope. The initial beam current measurements and the quantum yield curves are consistent and demonstrate that there is significant contrast between labeled and unlabeled proteins. However, after several minutes in the photoelectron microscope, the proteins become more photoemissive and the contrast diminishes. This change in contrast explains several puzzling observations in the literature.

Characterization of the binding of Triton X-100 to equine and rabbit serum albumin.

The binding isotherms for Triton X-100 binding to equine and rabbit serum albumin were determined by equilibrium dialysis at 16 degrees C in pH 7.0, I = 0.05 phosphate buffer. Presented in a Scatchard plot, the binding isotherms are a straight line, indicating thermodynamically independent and identical binding sites. In this model equine serum albumin is characterized as having 11 such sites with an equilibrium constant of 6.0 x 10(3) M-1. Similarly, rabbit serum albumin is characterized as having 9 such sites with an equilibrium constant of 8.0 x 10(3) M-1.

Binding of the Triton X series of nonionic surfactants to bovine serum albumin.

The binding of a series of Triton X nonionic surfactants (NIS) tobivine serum albumin (BSA) has been studied by equilibrium dialysis and titration calorimetry. At pH 7.0, Triton X molecules bind to two classes of sites, the first 2 molecules binding with positive cooperativity to high-affinity sites following by the binding of approximately 15 additional molecules to lower affinity, thermodynamically identical, and independent sites. The strength of the binding decreases as the number of oxyethylene units is increased in the surfactants Triton X-114, X-100, X-102, and X-165. Calorimetric measurements show the enthalpy change for the NIS-BSA interaction to be small and endothermic. Increasing the hydrophilic oxyethylene chain length results in a more endothermic enthalpy change and a smaller association constant. Electron spin resonance studies of Triton X binding to BSA, covalently spin-labeled with N-(2,2,6,6-tetramethyl-piperidinyl-1-oxy)maleimide, indicated that the protein conformation in the vicinity of the labeled sulfhydryl was insensitive to NIS binding from dilute monomeric solutions. Calorimetric experiments near the critical micelle concentration indicate, however, that the protein probably undergoes a conformational change associated with the population of the lower affinity NIS binding sites.

Evidence for differences in the binding of triton X-100 to sheep and human serum albumins.

The binding of triton X-100 to bovine serum albumin has been shown to exhibit positive cooperativity. Subsequent equilibrium dialysis studies indicate that the binding of Triton X-100 to sheep serum albumin likewise shows positive cooperativity, the first two stepwise equilibrium constants being K1 = 1.24 X 10(4) M-1 and K2 = 1.62 X 10(4) M-1. However, the mechanism for Triton X-100 binding to human serum albumin differs in that the binding isotherm indicates the binding sites are independent and identical. In the latter case the binding is described by the Scatchard model with an equilibrium constant of K = 7.2 X 10(3) M-1. The studies were conducted at 16 degrees C in pH 7.0, I = 0.05 phosphate buffer.

Binding of Triton X-114 to mammalian serum albumins at critical micelle concentration.

When the nonionic detergent Triton X-114 binds to different mammalian serum albumins, remarkably little variation occurs in the number bound at the critical micelle concentration of the detergent. Average molar ratios range from 4.0 to 6.3; mean body weights range from 0.25 to 600 kg. Measured values of the extinction coefficients reported here also show remarkably little variation. These results support the view that the folding of these serum albumins is similar.