29 research outputs found
Complete experimental toolbox for alignment-free quantum communication
Quantum communication employs the counter-intuitive features of quantum
physics to perform tasks that are im- possible in the classical world. It is
crucial for testing the foundations of quantum theory and promises to rev-
olutionize our information and communication technolo- gies. However, for two
or more parties to execute even the simplest quantum transmission, they must
establish, and maintain, a shared reference frame. This introduces a
considerable overhead in communication resources, par- ticularly if the parties
are in motion or rotating relative to each other. We experimentally demonstrate
how to circumvent this problem with the efficient transmission of quantum
information encoded in rotationally invariant states of single photons. By
developing a complete toolbox for the efficient encoding and decoding of
quantum infor- mation in such photonic qubits, we demonstrate the fea- sibility
of alignment-free quantum key-distribution, and perform a proof-of-principle
alignment-free entanglement distribution and violation of a Bell inequality.
Our scheme should find applications in fundamental tests of quantum mechanics
and satellite-based quantum communication.Comment: Main manuscript: 7 pages, 3 figures; Supplementary Information: 7
pages, 3 figure
Ligand-Directed Chemistry on Glycoside Hydrolases – A Proof of Concept Study
Selective covalent labelling of enzymes using small molecule probes has advanced the scopes of protein profiling. The covalent bond formation to a specific target is the key step of activity-based protein profiling (ABPP), a method which has become an indispensable tool for measuring enzyme activity in complex matrices. With respect to carbohydrate processing enzymes, strategies for ABPP so far involve labelling the active site of the enzyme, which results in permanent loss of activity. Here, we report in a proof of concept study the use of ligand-directed chemistry (LDC) for labelling glycoside hydrolases near – but not in – the active site. During the labelling process, the competitive inhibitor is cleaved from the probe, departs the active site and the enzyme maintains its catalytic activity. To this end, we designed a building block synthetic concept for small molecule probes containing iminosugar-based reversible inhibitors for labelling of two model β-glucosidases. The results indicate that the LDC approach can be adaptable for covalent proximity labelling of glycoside hydrolases.T. M. W. thanks the FWF (Wien, Austria) for financial support (project number P30372-B21). Authors from TU Graz acknowledge support from NAWI Graz.Peer reviewe
Synthesis of N-protected Galactosamine Building Blocks from D-Tagatose via the Heyns Rearrangement
N-Alkylated Derivatives of 1,5-Dideoxy-1,5-iminoxylitol as Î’-Xylosidaseand Î’-Glucosidase Inhibitors
The Amadori rearrangement as glycoconjugation method: Synthesis of non-natural C-glycosyl type glycoconjugates
The Amadori rearrangement was investigated as a potential method for the conjugation of carbohydrate moieties to suitable amino components. Starting from selected aldoheptoses, which are readily available by means of the Kiliani–Fischer C-elongation reaction of the corresponding aldohexoses, glycoconjugates presenting D-gluco, D-manno and D-galacto as well as GlcNAc motifs have been synthesised. Following this strategy, non-natural C-glycosyl type glycoconjugates, which can be utilised as building blocks for the composition of larger molecular constructions, are available by a very short synthetic approach