Superresolved, 3D, multi-fluorophore tracking of live-cell dynamics

Lead Research Organisation: Science and Technology Facilities Council
Department Name: Central Laser Facility (CLF)

Abstract

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Technical Summary

This multi-disciplinary proposal will address a 'technology gap' in 'bioimaging and functional analysis', by making quantitative, high-resolution, 3D, time-resolved, information available from a new class of image data in fluorescence microscopy. We will develop new software tools for the capture and analysis of images to facilitate studies of fast, dynamic and 3D processes in live-cell biology, made accessible by recent optical and algorithmic developments.
The imaging technique involved uses a simple and inexpensive (~£5-6000) microscope attachment that provides between 2 and 9 different specimen planes simultaneously in focus on a single camera.
Spatial resolution better than 10nm has been shown to be routinely available in test measurements and from a single camera frame. The in-focus planes can be designed to cover the full depth of a cell (i.e. ~10 microns).
The technique uses a combination of the microscope attachment described above, with wavefront-sensing techniques derived from the exploitation of 'adaptive optics' in astronomy and a Maximum Likelihood algorithm, for superresolved determination of the depth of particles within the specimen. This will be combined with advanced tracking algorithms previously developed within our group.
We will develop and distribute software that will allow microscopy groups both to design a microscope attachment suitable their particular application and to analyse the data that that imaging system provides.

Planned Impact

The principal academic beneficiaries are microscopists wishing to track fluorescent particles (e.g. vesicles) and fast-dynamic processes with high spatial resolution in live-cell microscopy and for whom the programme will make these technologies easily and openly accessible. In particular, by providing data on the dynamics associated with organelles in both normal and dysfunctional cells this study can make contributions to the understanding of important processes such as exocytosis, endocytosis, the dynamics of cytoskeletal structure and cargo transport.

Benefit will also available to microscopists working on fixed cells where a z-stack is required, but there are problems associated with bleaching of fluorophores.

For biologists working in these areas it is intended that the results from this programme, together will all optical designs, will become openly available shortly after the programme ends and the systems are as bug-free and user-friendly as is practical. For UK biologists we anticipate that dissemination of the results and system through our web site and through the contacts that we have established with biologists involved as investigators will occur rapidly and even during the programme (for those willing to work with systems still under development - indeed such interactions can strengthen our work in the later stages). For non-UK biologists we wish also to make all software and hardware freely available to those who wish to have such information, and will ensure open access at the earliest possible point. We see providing support to companies who in turn provide equipment to microscopists as a valuable method to assist wider dissemination.

Wider benefit from this work will be found in many fluid-flow areas, such as the fluid-flow in heat exchangers, the analysis of mixing in fuel systems and bioreactors, flow in food-drying towers, flow through porous media (in the context of models of such flow based on transparent constructions), applications in contexts such as the oil industry for monitoring the distribution and motion of and oil mixtures in sea-water pumped through wells in the later stages of oil extraction from wells in remote locations (esp the sea bed). In the context of fuel mixing, even minor fuel efficiencies achieved through improved understanding of these issues can lead to very-substantial savings and thus contribute to the reduction in emissions of both CO2 and particulate matter.

In addition, because the techniques considered here are clearly capable of achieving high-precision metrology measurements, the longer-term, prospects of surface-shape measurement may provide a useful tool for manufacturing.

Publications

10 25 50
 
Description The grant enabled the construction of a multifocal microscope at Rutherford Appleton Laboratory and has provided software that enables data from the microscope to be analysed.

This has been used to initiate a collaboration with the University of Manchester to develop a method of determining the effects of shear stress on cellular morphology and calcium expression at the subcellular level. Two publications are currently in progress to disseminate this work.
Exploitation Route This is a new research facility within the Octopus facility, which is made available through the Central Laser Facility's usual peer review process. Commercial and academic users are invited to apply for time on the microscope and initiate new collaborations with us.
Sectors Chemicals,Healthcare,Manufacturing, including Industrial Biotechology,Pharmaceuticals and Medical Biotechnology

 
Description Facility Access to Central Laser Facility
Amount £1,000 (GBP)
Funding ID 16130044 
Organisation Science and Technologies Facilities Council (STFC) 
Sector Public
Country United Kingdom
Start 05/2016 
End 05/2017
 
Description Facility Access to Central Laser Facility
Amount £1,000 (GBP)
Funding ID 16130035 
Organisation Science and Technologies Facilities Council (STFC) 
Sector Public
Country United Kingdom
Start 05/2016 
End 03/2017
 
Description Facility Access to Central Laser Facility
Amount £1,000 (GBP)
Funding ID 15230040 
Organisation Science and Technologies Facilities Council (STFC) 
Sector Public
Country United Kingdom
Start 01/2016 
End 04/2016
 
Title Flow studies 
Description Multifocal imaging is a new method of studying the effects of shear stress on osteoblast cells. Flow fields around cultured cells are measured in 3D using fluorescent beads and correlated with the biochemical effects on the cells. Shear stress is important because it affects bone growth. 
Type Of Material Model of mechanisms or symptoms - in vitro 
Year Produced 2016 
Provided To Others? Yes  
Impact The bone tissue engineering group at the University of Manchester have been awarded time on the Octopus facility at Rutherford Appleton Laboratory to take these experiments further. 
 
Description HW-RAL 
Organisation Heriot-Watt University
Country United Kingdom 
Sector Academic/University 
PI Contribution We share an EngD student. We provide expertise in single-molecule imaging and superresolution imaging to demonstrate the utility of Heriot Watt's multiplane setup.
Collaborator Contribution Heriot Watt co-supervise the student. They provide expertise in multifocal imaging that has allowed their setup to be replicated at RAL.
Impact None as yet
Start Year 2013
 
Description Applied Photonics EngD conference (Edinburgh) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Postgraduate students
Results and Impact ~50 EngD students and ~30 academics and others attended the Centre for Doctoral Training in Applied Photonics Annual Conference. An EngD student who worked on the research covered by this awarded gave a talk, assisting in the training of his fellow postgraduate students by contributing to the demonstration of the wide applications of photonics.
Year(s) Of Engagement Activity 2016
URL http://www.cdtphotonics.hw.ac.uk/sites/www.cdtphotonics.hw.ac.uk/files/CDTAP%20handbook%202016%20.pd...
 
Description Scottish Microscopy Group symposium (Edinburgh) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Professional Practitioners
Results and Impact EngD student gave talk on multifocal microscopy to ~30 members of the Scottish Microscopy Group, which led to questions and discussion about the technique.
Year(s) Of Engagement Activity 2016
URL http://scottishmicroscopygroup.org.uk/symposia/2016-symposium