Evidence for the interaction of Endophilin A3 with endogenous K(Ca)2.3 channels in PC12 cells

Background/Aims: Small-conductance calcium-activated (SK) channels play an important role by controlling the after-hyperpolarization of excitable cells. The level of expression and density of these channels is an essential factor for controlling different cellular functions. Several studies showed a co-localization of KCa2.3 channels and Endophilin A3 in different tissues. Endophilin A3 belongs to a family of BAR- and SH3 domain containing proteins that bind to dynamin and are involved in the process of vesicle scission in clathrin-mediated endocytosis. Methods: Using the yeast two-hybrid system and the GST pull down assay we demonstrated that Endophilin A3 interacts with the N-terminal part of KCa2.3 channels. In addition, we studied the impact of this interaction on channel activity by patch clamp measurements in PC12 cells expressing endogenous KCa2.3 channels. KCa2.3 currents were activated by using pipette solutions containing 1 µM free Ca(2+). Results: Whole-cell measurements of PC12 cells transfected with Endophilin A3 showed a reduction of KCa2.3 specifc Cs(+) currents indicating that the interaction of Endophilin A3 with KCa2.3 channels also occurs in mammalian cells and that this interaction has functional consequences for current flowing through KCa2.3 channels. Since KCa2.3 specific currents could be increased in PC12 cells transfected with Endophilin A3 with DC-EBIO (30 µM), a known SK-channel activator, these data also implicate that Endophilin A3 did not significantly remove KCa2.3 channels from the membrane but changed the sensitivity of the channels to Ca(2+) which could be overcome by DC-EBIO. Conclusion: This interaction seems to be important for the function of KCa2.3 channels and might therefore play a significant role in situations where channel activation is pivotal for cellular function

Inelastic and transfer reactions in 92Mo+255 MeV 60Ni collisions studied by γγ coincidences

For the 92Mo+255 MeV60Ni system, inelastic and few-nucleon transfer events populating non-collective states of moderately high spin have been studied by γγ coincidence measurements. Besides the strong inelastic scattering channel, twelve transfer processes were identified, ranging from 1 n to 2α transfer; typically, cross coincidences between the γ-rays from both products were observed. Potential spectroscopic applications are indicated

Structure in the E2 quasicontinuum spectrum of Dy154

The evolution of the quasicontinuum spectrum with neutron number has been investigated in the sequence of isotopes Dy152,154,156. The three nuclei display a pronounced collective E2 component. In Dy154 this component shows a splitting into two distinct parts, signifying a structural change along the cascade above the yrast line. The E2 and statistical components are reproduced in simple -cascade calculations; in Dy152 and Dy156 only rotational bands are included, whereas in Dy154 additional vibration-like transitions are required to reproduce the two E2 peaks

Structural changes along and above the yrast line of Dy154

States in Dy154 have been located up to I=48+ and their lifetimes measured. Marked structural changes occur along the yrast line with a transition from prolate to oblate shape, followed by an unexpected return to moderate collectivity at the highest spins. Structural changes with increasing energy above the yrast line are also observed

Lifetime measurements of terminating and collective high-spin states in 155DY^{155}DY and 156DY^{156}DY

Lifetime measurements for the isotopes 155Dy and 156Dy have been extended up to spins around 40h{stroke} by the Doppler shift attenuation method in conjunction with γ-γ-coincidence measurements. Results have been obtained for the yrast band in 156Dy and for three bands in 155Dy. Strong retardations of the E2-strengt were observed for intruding terminating sequences, for which specific single particle configurations are suggested