Intrinsic time gravity and the Lichnerowicz-York equation

We investigate the effect on the Hamiltonian structure of general relativity of choosing an intrinsic time to fix the time slicing. 3-covariance with momentum constraint is maintained, but the Hamiltonian constraint is replaced by a dynamical equation for the trace of the momentum. This reveals a very simple structure with a local reduced Hamiltonian. The theory is easily generalised; in particular, the square of the Cotton-York tensor density can be added as an extra part of the potential while at the same time maintaining the classic 2 + 2 degrees of freedom. Initial data construction is simple in the extended theory; we get a generalised Lichnerowicz-York equation with nice existence and uniqueness properties. Adding standard matter fields is quite straightforward.Comment: 4 page

Quantum Key Distribution Using Quantum Faraday Rotators

We propose a new quantum key distribution (QKD) protocol based on the fully quantum mechanical states of the Faraday rotators. The protocol is unconditionally secure against collective attacks for multi-photon source up to two photons on a noisy environment. It is also robust against impersonation attacks. The protocol may be implemented experimentally with the current spintronics technology on semiconductors.Comment: 7 pages, 7 EPS figure

Equivalence between various versions of the self-dual action of the Ashtekar formalism

Different aspects of the self-dual (anti-self-dual) action of the Ashtekar canonical formalism are discussed. In particular, we study the equivalences and differences between the various versions of such an action. Our analysis may be useful for the development of an Ashtekar formalism in eight dimensions.Comment: 10 pages, Latex, minor correction

Constraints of FL Motif on the Targeting and Function of Sodium-Bicarbonate Cotransporter 1

A C-terminal dihydrophobic FL motif plays a vital role in the basolateral targeting of sodium bicarbonate cotransporter 1. To further characterize the role of dihydrophobic FL motif, 1). the FL motif in wild type (PFLS) was reversed to LF (PLFS), 2). the FL motif (PFLS) was shifted upstream (FLPS), and 3). the FL motif (PFLS) was shifted downstream (PSFL). The wild type (PFLS) and its mutant (PLFS) were exclusively expressed on the basolateral membrane by con-focal microscopy, however, the mutant (FLPS) and (PSFL) were predominantly mistargeted to the apical membrane and the cytoplasm, respectively. Functional studies showed that the mutant (PSFL) displayed a remarkably reduced current (p value<0.05 vs wild type). The mutant (PSFL) displayed a more reduced membrane surface expression than the wild type and was co-localized with ER marker. The protein sequence spanning FL motif in kNBC1 C-terminal cytoplasmic tail shows a helical structure, mutants (PLFS) and (PSFL) reduce a-helical contents by circular dichroism study. Reversed FL isn't a constraint for basolateral targeting, but shifting it upstream and downstream are ones