University of Queensland

About: University of Queensland is a education organization based out in Brisbane, Queensland, Australia. It is known for research contribution in the topics: Population & Poison control. The organization has 51138 authors who have published 155721 publications receiving 5717659 citations. The organization is also known as: UQ & The University of Queensland.

Simplifying quantum logic using higher-dimensional Hilbert spaces

Abstract: Quantum computation promises to solve fundamental, yet otherwise intractable, problems across a range of active fields of research. Recently, universal quantum logic-gate sets—the elemental building blocks for a quantum computer—have been demonstrated in several physical architectures. A serious obstacle to a full-scale implementation is the large number of these gates required to build even small quantum circuits. Here, we present and demonstrate a general technique that harnesses multi-level information carriers to significantly reduce this number, enabling the construction of key quantum circuits with existing technology. We present implementations of two key quantum circuits: the three-qubit Toffoli gate and the general two-qubit controlled-unitary gate. Although our experiment is carried out in a photonic architecture, the technique is independent of the particular physical encoding of quantum information, and has the potential for wider application.

Generation of Hyperentangled Photon Pairs

Abstract: We experimentally demonstrate the first quantum system entangled in every degree of freedom (hyperentangled). Using pairs of photons produced in spontaneous parametric down-conversion, we verify entanglement by observing a Bell-type inequality violation in each degree of freedom: polarization, spatial mode, and time energy. We also produce and characterize maximally hyperentangled states and novel states simultaneously exhibiting both quantum and classical correlations. Finally, we report the tomography of a $2\ifmmode\times\else\texttimes\fi{}2\ifmmode\times\else\texttimes\fi{}3\ifmmode\times\else\texttimes\fi{}3$ system (36-dimensional Hilbert space), which we believe is the first reported photonic entangled system of this size to be so characterized.

T-cell activation by transitory neo-antigens derived from distinct microbial pathways

Abstract: T cells discriminate between foreign and host molecules by recognizing distinct microbial molecules, predominantly peptides and lipids. Riboflavin precursors found in many bacteria and yeast also selectively activate mucosal-associated invariant T (MAIT) cells, an abundant population of innate-like T cells in humans. However, the genesis of these small organic molecules and their mode of presentation to MAIT cells by the major histocompatibility complex (MHC)-related protein MR1 (ref. 8) are not well understood. Here we show that MAIT-cell activation requires key genes encoding enzymes that form 5-amino-6-d-ribitylaminouracil (5-A-RU), an early intermediate in bacterial riboflavin synthesis. Although 5-A-RU does not bind MR1 or activate MAIT cells directly, it does form potent MAIT-activating antigens via non-enzymatic reactions with small molecules, such as glyoxal and methylglyoxal, which are derived from other metabolic pathways. The MAIT antigens formed by the reactions between 5-A-RU and glyoxal/methylglyoxal were simple adducts, 5-(2-oxoethylideneamino)-6-D-ribitylaminouracil (5-OE-RU) and 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil (5-OP-RU), respectively, which bound to MR1 as shown by crystal structures of MAIT TCR ternary complexes. Although 5-OP-RU and 5-OE-RU are unstable intermediates, they became trapped by MR1 as reversible covalent Schiff base complexes. Mass spectra supported the capture by MR1 of 5-OP-RU and 5-OE-RU from bacterial cultures that activate MAIT cells, but not from non-activating bacteria, indicating that these MAIT antigens are present in a range of microbes. Thus, MR1 is able to capture, stabilize and present chemically unstable pyrimidine intermediates, which otherwise convert to lumazines, as potent antigens to MAIT cells. These pyrimidine adducts are microbial signatures for MAIT-cell immunosurveillance.