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Path-polarization hyperentangled and cluster states of photons on a chip.

ABSTRACT: Encoding many qubits in different degrees of freedom (DOFs) of single photons is one of the routes toward enlarging the Hilbert space spanned by a photonic quantum state. Hyperentangled photon states (that is, states showing entanglement in multiple DOFs) have demonstrated significant implications for both fundamental physics tests and quantum communication and computation. Increasing the number of qubits of photonic experiments requires miniaturization and integration of the basic elements, and functions to guarantee the setup stability, which motivates the development of technologies allowing the precise control of different photonic DOFs on a chip. We demonstrate the contextual use of path and polarization qubits propagating within an integrated quantum circuit. We tested the properties of four-qubit linear cluster states built on both DOFs, and we exploited them to perform the Grover's search algorithm according to the one-way quantum computation model. Our results pave the way toward the full integration on a chip of hybrid multi-qubit multiphoton states.

SUBMITTER: Ciampini MA

PROVIDER: S-EPMC6059950 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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Path-polarization hyperentangled and cluster states of photons on a chip.

Ciampini Mario Arnolfo MA Orieux Adeline A Paesani Stefano S Sciarrino Fabio F Corrielli Giacomo G Crespi Andrea A Ramponi Roberta R Osellame Roberto R Mataloni Paolo P

Light, science & applications 20160422 4

Encoding many qubits in different degrees of freedom (DOFs) of single photons is one of the routes toward enlarging the Hilbert space spanned by a photonic quantum state. Hyperentangled photon states (that is, states showing entanglement in multiple DOFs) have demonstrated significant implications for both fundamental physics tests and quantum communication and computation. Increasing the number of qubits of photonic experiments requires miniaturization and integration of the basic elements, and ...[more]

PMID: 30167159

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Project description:BackgroundHistone post-translational modifications (PTMs) are key epigenetic regulators in chromatin-based processes. Increasing evidence suggests that vast combinations of PTMs exist within chromatin histones. These complex patterns, rather than individual PTMs, are thought to define functional chromatin states. However, the ability to interrogate combinatorial histone PTM patterns at the nucleosome level has been limited by the lack of direct molecular tools.ResultsHere we demonstrate an efficient, quantitative, antibody-free, chromatin immunoprecipitation-less (ChIP-less) method for interrogating diverse epigenetic states. At the heart of the workflow are recombinant chromatin reader domains, which target distinct chromatin states with combinatorial PTM patterns. Utilizing a newly designed combinatorial histone peptide microarray, we showed that three reader domains (ATRX-ADD, ING2-PHD and AIRE-PHD) displayed greater specificity towards combinatorial PTM patterns than corresponding commercial histone antibodies. Such specific recognitions were employed to develop a chromatin reader-based affinity enrichment platform (matrix-assisted reader chromatin capture, or MARCC). We successfully applied the reader-based platform to capture unique chromatin states, which were quantitatively profiled by mass spectrometry to reveal interconnections between nucleosomal histone PTMs. Specifically, a highly enriched signature that harbored H3K4me0, H3K9me2/3, H3K79me0 and H4K20me2/3 within the same nucleosome was identified from chromatin enriched by ATRX-ADD. This newly reported PTM combination was enriched in heterochromatin, as revealed by the associated DNA.ConclusionsOur results suggest the broad utility of recombinant reader domains as an enrichment tool specific to combinatorial PTM patterns, which are difficult to probe directly by antibody-based approaches. The reader affinity platform is compatible with several downstream analyses to investigate the physical coexistence of nucleosomal PTM states associated with specific genomic loci. Collectively, the reader-based workflow will greatly facilitate our understanding of how distinct chromatin states and reader domains function in gene regulatory mechanisms.

Dataset Information

Path-polarization hyperentangled and cluster states of photons on a chip.

Publications

Path-polarization hyperentangled and cluster states of photons on a chip.

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