QUANTUM4BIO · Quantum Optics Tools for Biomedical Imaging
FP7 — People (Marie Curie Actions)
- Duration
- 2012-06-01 → 2014-05-31
- EU contribution
- €180,191
- Participants
- 1
- Scheme
- MC-IIF
Lines connect the coordinator with its partners.
Results in brief
Quantum Optics Tools for Biomedical Imaging
Optical imaging techniques have undergone a renaissance over the recent years and are powerful and omnipresent tools in current biological research. They provide three dimensional structural and functional information of biological samples and have led to new and important insights that help to understand the structure and dynamic of cellular processes at different levels. One widely used technique is two-photon fluorescence microscopy (TPFM), which has the advantage of improved depth penetration due to the longer wavelengths used and reduced photo-bleaching of chromophores. Unfortunately, it requires expensive laser light sources and high light intensities. In this project, we investigated the use of alternative, non classical light sources for their use in biological research. In typical biological samples, the two-photon absorption coefficient is very small and high light intensities are required to facilitate two-photon interactions. However, there exist light sources that might be better suited to this type of imaging. Non-classical sources of light, also known as entangled light sources, feature intrinsic energy-time correlation which significantly increases the absorption efficiency of TPFM. Such correlated light sources further have a non-Poissonian emission statistics, which allows controlling the exact amount of light as measured by individual light quanta, or photons, to be directed to the biological sample. During the reporting period of this project, the researchers were successful in designing and setting-up a broadband source of correlated photons based on spontaneous parametric down-conversion (SPDC). It provides up to 0.2uW (or 10^13 photons per second) of optical power, and due to it’s high bandwidth of ~100nm, features ultra-fast coherence times of ~18fs. Using these novel light sources we have set up an international collaboration with researchers at the University of Waterloo, Canada (IQC), which are aimed at investigating the two-photon excitation of different fluorescent molecules under different conditions. Our results so far have indicated that compensation of dispersion properties of these photons are extremely important and highly delicate. Parallel to this efforts,alternative applications of quantum states of light in the biomedical research fields had been identified, for which we have designed and built a SPDC source that allows to investigate the interaction of individual photons from the SPDC source with bio-molecules. In this context the efficient generation and detection of time-energy entangled SPDC light offers the advantage of well-defined photon number states, so-called Fock states. Detection of photons in the idler beam heralds a Fock-state in the signal arm. Therefore one can infer with low uncertainty the number of photons present in a given “pulse”. This is in contrast to classical laser light, which – even when appropriately attenuated – retains a Poissonian and therefore quasi-random distribution of photon numbers. Using quantum states of light with well-defined photon numbers could shed light onto the exact timing and interaction mechanism of light sensitive biological molecules. Experiments in this direction are currently underway in our lab.
Data: CORDIS, © European Union
Project objective
Two-photon fluorescence microscopy has evolved to one of the most powerful tools in biological imaging, especially in the field of neuroscience. It provides improved depth penetration and reduced photo-bleaching of fluorophores and has thus enabled three dimensional structural and functional imaging of biological samples. However, in typical media and with uncorrelated (classical) photons, the two-photon absorption (TPA) process has small interaction strengths and therefore requires large optical intensities, which can lead to photo-damage in the media or prohibit its use with highly light sensitive biological samples.In this fellowship, we will address this shortcoming by using the process of entangled two-photon absorption (ETPA). Due to the energy-time correlation of entangled photon pairs, the effective cross-section, and therefore the efficiency of the absorption, can be increased by many orders of magnitude. This represents a fundamentally new approach to microscopy and if successful, will have a significant impact on fundamental and applied biology, as it allows for imaging and probing biological processes in a highly non-invasive fashion.For this project, we aim to design and build an entangled photon source engineered for optimal ETPA and identify ideal molecules that can function as labels and fluorescent proteins in biological samples. This highly interdisciplinary project will combine and exploit advantages of quantum optics and two-photon fluorescence microscopy and pave the way for novel, entanglement-based biological imaging and spectroscopy tools. This highly interdisciplinary project will combine the candidate’s expertise in quantum optics and quantum information with the host’s extensive background in bio-medical imaging. This fellowship will catalyze a significant development in the candidate’s career and enable him to attain a leading independent position in this new field at the interface of quantum physics and biology.""
Original text from CORDIS.
Participants
- UNIVERSITAT WIEN · WienCoordinatorAustria
Links
Data: CORDIS, © European Union
