Coherent information analysis of quantum channels in simple quantum systems

The coherent information concept is used to analyze a variety of simple quantum systems. Coherent information was calculated for the information decay in a two-level atom in the presence of an external resonant field, for the information exchange between two coupled two-level atoms, and for the information transfer from a two-level atom to another atom and to a photon field. The coherent information is shown to be equal to zero for all full-measurement procedures, but it completely retains its original value for quantum duplication. Transmission of information from one open subsystem to another one in the entire closed system is analyzed to learn quantum information about the forbidden atomic transition via a dipole active transition of the same atom. It is argued that coherent information can be used effectively to quantify the information channels in physical systems where quantum coherence plays an important role.Comment: 24 pages, 7 figs; Final versiob after minor changes, title changed; to be published in Phys. Rev. A, September 200

Theory of dark resonances for alkali vapors in a buffer-gas cell

We develop an analytical theory of dark resonances that accounts for the full atomic-level structure, as well as all field-induced effects such as coherence preparation, optical pumping, ac Stark shifts, and power broadening. The analysis uses a model based on relaxation constants that assumes the total collisional depolarization of the excited state. A good qualitative agreement with experiments for Cs in Ne is obtained.Comment: 16 pages; 7 figures; revtex4. Accepted for publication in PR

Entanglement transfer between bipartite systems

The problem of a controlled transfer of an entanglement initially encoded into two two-level atoms that are successively sent through two single-mode cavities is investigated. The atoms and the cavity modes form a four qubit system and we demonstrate under which conditions the initial entanglement encoded into the atoms can be completely transferred to other pairs of qubits. We find that in the case of a nonzero detuning between the atomic transition frequencies and the cavity mode frequencies, no complete transfer of the initial entanglement is possible to any of the other pairs of qubits. In the case of exact resonance and equal coupling strengths of the atoms to the cavity modes, an initial maximally entangled state of the atoms can be completely transferred to the cavity modes. The complete transfer of the entanglement is restricted to the cavity modes only with the transfer to the other pairs being limited to up to 50%. We have found that the complete transfer of an initial entanglement to other pairs of qubits may take place if the initial state is not the maximally entangled state and the atoms couple to the cavity modes with unequal strengths. Depending on the ratio between the coupling strengths, the optimal entanglement can be created between the atoms and one of the cavity modes.Comment: 3 figures. Oral talk presented in CEWQO 18, Madrid 201

Analysis of radiatively stable entanglement in a system of two dipole-interacting three-level atoms

We explore the possibilities of creating radiatively stable entangled states of two three-level dipole-interacting atoms in a $\Lambda$ configuration by means of laser biharmonic continuous driving or pulses. We propose three schemes for generation of entangled states which involve only the lower states of the $\Lambda$ system, not vulnerable to radiative decay. Two of them employ coherent dynamics to achieve entanglement in the system, whereas the third one uses optical pumping, i.e., an essentially incoherent process.Comment: Replaced with the final version; 14 pages, 6 figures; to appear in Phys. Rev. A, vol. 61 (2000

Phosphatidylinositol(4,5)bisphosphate coordinates actin-mediated mobilization and translocation of secretory vesicles to the plasma membrane of chromaffin cells

ORP5 and ORP8, members of the oxysterol-binding protein (OSBP)-related proteins (ORP) family, are endoplasmic reticulum membrane proteins implicated in lipid trafficking. ORP5 and ORP8 are reported to localize to endoplasmic reticulum-plasma membrane junctions via binding to phosphatidylinositol-4-phosphate (PtdIns(4)P), and act as a PtdIns(4)P/phosphatidylserine counter exchanger between the endoplasmic reticulum and plasma membrane. Here we provide evidence that the pleckstrin homology domain of ORP5/8 via PtdIns(4,5)P 2, and not PtdIns(4)P binding mediates the recruitment of ORP5/8 to endoplasmic reticulum-plasma membrane contact sites. The OSBP-related domain of ORP8 can extract and transport multiple phosphoinositides in vitro, and knocking down both ORP5 and ORP8 in cells increases the plasma membrane level of PtdIns(4,5)P 2 with little effect on PtdIns(4)P. Overall, our data show, for the first time, that phosphoinositides other than PtdIns(4)P can also serve as co-exchangers for the transport of cargo lipids by ORPs.ORP5/8 are endoplasmic reticulum (ER) membrane proteins implicated in lipid trafficking that localize to ER-plasma membrane (PM) contacts and maintain membrane homeostasis. Here the authors show that PtdIns(4,5)P 2 plays a critical role in the targeting and function of ORP5/8 at the PM

Phospholipase D signaling: orchestration by PIP2 and small GTPases

Hydrolysis of phosphatidylcholine by phospholipase D (PLD) leads to the generation of the versatile lipid second messenger, phosphatidic acid (PA), which is involved in fundamental cellular processes, including membrane trafficking, actin cytoskeleton remodeling, cell proliferation and cell survival. PLD activity can be dramatically stimulated by a large number of cell surface receptors and is elaborately regulated by intracellular factors, including protein kinase C isoforms, small GTPases of the ARF, Rho and Ras families and, particularly, by the phosphoinositide, phosphatidylinositol 4,5-bisphosphate (PIP2). PIP2 is well known as substrate for the generation of second messengers by phospholipase C, but is now also understood to recruit and/or activate a variety of actin regulatory proteins, ion channels and other signaling proteins, including PLD, by direct interaction. The synthesis of PIP2 by phosphoinositide 5-kinase (PIP5K) isoforms is tightly regulated by small GTPases and, interestingly, by PA as well, and the concerted formation of PIP2 and PA has been shown to mediate receptor-regulated cellular events. This review highlights the regulation of PLD by membrane receptors, and describes how the close encounter of PLD and PIP5K isoforms with small GTPases permits the execution of specific cellular functions