896 research outputs found

    Purification of the head-pieces of the elementary particles from beef heart mitochondria: their morphological structure and enzymatic activity

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    1. In order to obtain direct evidence for the enzymatic identification of the head-pieces of the elementary particles in the inner mitochondrial membrane, the head-pieces were detached by sonication from the isolated inner membrane of beef heart mitochondria, purified by pursuing the particles with the electron microscope, and analyzed for enzymatic properties. 2. Electron microscope examination revealed that the isolated headpieces are the spherical particles about 90&#192; in diameter which are quite similar in appearance to the head-pieces of the elementary particles lining the inner mitochondrial membranes. 3. The head-pieces are identified as ATPase sensitive to oligomysin when attached by stalks to the membrane, and become insensitive when detached or purified from the membrane. 4. The head-piece is labile to cold with respect to ATPase activity and morphology.</p

    Studies of transverse and longitudinal relaxations of 55^{55}Mn in molecular cluster magnet Mn12_{12}Ac

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    The transverse and longitudinal relaxation rates 1/T2T_2 and 1/T1T_1 of 55^{55}Mn in molecular cluster magnet Mn12_{12}Ac have been measured al low temperatures down to 200mK and in the fields upto 9T. Both of 1/T2T_2 and 1/T1T_1 exhibit remarkable decreases with decreasing temperature and with increasing field, with the relative relation T1/T2200T_1/T_2 \approx 200. In the analysis, we adopt a simple model that the thermal fluctuation of the cluster spin SS=10 associated with the spin-phonon interactionis, is only due to the excitation to the first excited state from the ground state with the average life-times τ1\tau_ 1 and τ0\tau_0 (τ0\tau_ 0\ggτ1\tau_1). We show that 1/T2T_2 is interpreted in terms of the strong collision regime as given by 1/τ0\tau_ 0, and that 1/T1T_1 is understood by the high-frequency limit based on standard perturbation treatment for the step-wise fluctuating field, thus being proportional to 1/τ0ωN2\tau_0\omega_N^2.Comment: 12 pages, 11 fugures, revtex

    Molecular basis for the disruption of Keap1–Nrf2 interaction via Hinge & Latch mechanism

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    The Keap1-Nrf2 system is central for mammalian cytoprotection against various stresses and a drug target for disease prevention and treatment. One model for the molecular mechanisms leading to Nrf2 activation is the Hinge-Latch model, where the DLGex-binding motif of Nrf2 dissociates from Keap1 as a latch, while the ETGE motif remains attached to Keap1 as a hinge. To overcome the technical difficulties in examining the binding status of the two motifs during protein-protein interaction (PPI) simultaneously, we utilized NMR spectroscopy titration experiments. Our results revealed that latch dissociation is triggered by low-molecular-weight Keap1-Nrf2 PPI inhibitors and occurs during p62-mediated Nrf2 activation, but not by electrophilic Nrf2 inducers. This study demonstrates that Keap1 utilizes a unique Hinge-Latch mechanism for Nrf2 activation upon challenge by non-electrophilic PPI-inhibiting stimuli, and provides critical insight for the pharmacological development of next-generation Nrf2 activators targeting the Keap1-Nrf2 PPI

    Proton Decay in the Semi-Simple Unification

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    Semi-simple unification is one of a model which naturally solves two difficulties in the supersymmetric grand unification theory: doublet-triplet splitting problem and suppression of dimension 5 proton decay. We analyzed the dimension 6 proton decay of this model using perturbative analysis at the next-to-leading order. The life time of proton is 3 \times 10^{34} - 10^{35} years for wide range of SUSY breaking parameters, and there is an intriguing possibility of observing proton decay signals in the next-generation water Cherenkov detectors such as Hyper-Kamiokande and TITAND. Several uncertainties in this prediction are also discussed.Comment: 16 pages, including 2 tables and 3 figures, UT-97

    Signal for supernova νμ\nu_\mu and ντ\nu_\tau neutrinos in water \v{C}erenkov detectors

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    We suggest that photons with energies between 5 and 10 MeV, generated by the (ν,νpγ\nu,\nu'p\gamma) and (ν,νnγ\nu,\nu'n\gamma) reactions on 16^{16}O, constitute a signal which allows a unique identification of supernova νμ\nu_\mu and ντ\nu_\tau neutrinos in water \v{C}erenkov detectors. We calculate the yield of such γ\gamma events and estimate that a few hundred of them would be detected in Superkamiokande for a supernova at 10 kpc distance.Comment: 8 pages, RevTex 3.0, figures and text available at http://www.krl.caltech.edu/preprints/MAP.htm

    Novel diffusion mechanism on the GaAs(001) surface: the role of adatom-dimer interaction

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    Employing first principles total energy calculations we have studied the behavior of Ga and Al adatoms on the GaAs(001)-beta2 surface. The adsorption site and two relevant diffusion channels are identified. The channels are characterized by different adatom-surface dimer interaction. Both affect in a novel way the adatom migration: in one channel the diffusing adatom jumps across the surface dimers and leaves the dimer bonds intact, in the other one the surface dimer bonds are broken. The two channels are taken into account to derive effective adatom diffusion barriers. From the diffusion barriers we conclude a strong diffusion anisotropy for both Al and Ga adatoms with the direction of fastest diffusion parallel to the surface dimers. In agreement with experimental observations we find higher diffusion barriers for Al than for Ga.Comment: 4 pages, 2 figures, Phys. Rev. Lett. 79 (1997). Other related publications can be found at http://www.rz-berlin.mpg.de/th/paper.htm

    OPA1 and cardiolipin team up for mitochondrial fusion

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    Fusion between the inner membranes of two mitochondria requires the GTPase optic atrophy 1 (OPA1), but the molecular mechanism is poorly understood. A study now shows that fusion of two liposomes can be performed by OPA1 tethered to just one liposome, through an interaction with the phospholipid cardiolipin on the opposing liposome
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