Primed Conversion Oblique Plane Microscopy
Lead Research Organisation:
Imperial College London
Department Name: Bioengineering
Abstract
One of the most fundamental questions asked by even small children is 'where do I come from?' One interpretation of this question might be to explain how a single fertilized egg can grow into a fully functioning person. The intricate dance of chemical signals and cell motions that governs this process is complex, difficult to understand and, perhaps most surprisingly of all, reliable: for approximately 350,000 generations of humans in the 7 million years or so since humans evolved, this process has proceeded more or less successfully. Clearly, it is worthwhile understanding this process, not only from a medical perspective (in which we seek to treat diseases that occur during the growth of a baby) but also out of simple curiosity; the need to understand how the processes which formed us work.
One crucial aspect of this question is how a ball of cells knows which cells should form which parts of the body; why we don't normally end up with two heads, for example. One way to tackle this question is to label the cells when there are only a few of them, and then watch as this ball of cells develops into an embryo. If the label persists as the cell splits into more and more cells, we can follow the generations back to the original cell by looking for those which have this label. Currently there are a few ways to label a cell in this manner, but one of the most common is to add fluorescent molecules (i.e. molecules which glow when you shine light on them) to the cell; when it splits, these molecules end up in the two 'daughter' cells, and the process repeats. Dr Pantazis has pioneered a way to label individual cells in just this way by a technique called Primed Conversion. In Primed Conversion, the cell produces fluorescent proteins, but these proteins can be switched from green to red by shining two different coloured lights on them at the same time. Only regions where these two colours overlap undergo labelling.
Despite the power of Primed Conversion to label cells, its use has been limited to date, not because the technique is hard to use, but because to work most effectively a new type of microscope needs to be developed. This is where the Rowlands lab can help; this lab specializes in creating new types of microscopes and other optical systems. Dr Rowlands has designed a system that not only can make sure the two coloured lights overlap in exactly the right point in space, but can also image the cells as they split. A particularly powerful advantage of doing both processes on the same microscope is that, ordinarily, the red proteins get diluted when the cell splits. Using the new microscope, the signal can be 'topped up' every generation, so the cells can be traced over much longer periods of time. In addition, because the method for imaging the cells in this microscope (known as light-sheet fluorescence microscopy) is particularly kind to cells (it uses very low light levels so that the cells do not get exposed to too much light) it is very suitable for studying embryos which are very sensitive to light and other perturbations.
Ultimately this microscope will be used for other applications outside of embryology as well. For example, the same system can be used to perform super-resolution imaging, allowing it to see beyond the so-called 'diffraction limit' which prevents microscopes from seeing very small things like viruses. It can be used to track immune cells as they fight off an infection, to quantify blood flow, and investigate how cancer invades the body. The whole system was designed to work as an add-on to a normal microscope, letting scientists work with the kinds of tools they are familiar with, and probably already have in their labs. Finally, because we are strong believers in open access to science, all the plans, software and data will be released for anyone to use.
One crucial aspect of this question is how a ball of cells knows which cells should form which parts of the body; why we don't normally end up with two heads, for example. One way to tackle this question is to label the cells when there are only a few of them, and then watch as this ball of cells develops into an embryo. If the label persists as the cell splits into more and more cells, we can follow the generations back to the original cell by looking for those which have this label. Currently there are a few ways to label a cell in this manner, but one of the most common is to add fluorescent molecules (i.e. molecules which glow when you shine light on them) to the cell; when it splits, these molecules end up in the two 'daughter' cells, and the process repeats. Dr Pantazis has pioneered a way to label individual cells in just this way by a technique called Primed Conversion. In Primed Conversion, the cell produces fluorescent proteins, but these proteins can be switched from green to red by shining two different coloured lights on them at the same time. Only regions where these two colours overlap undergo labelling.
Despite the power of Primed Conversion to label cells, its use has been limited to date, not because the technique is hard to use, but because to work most effectively a new type of microscope needs to be developed. This is where the Rowlands lab can help; this lab specializes in creating new types of microscopes and other optical systems. Dr Rowlands has designed a system that not only can make sure the two coloured lights overlap in exactly the right point in space, but can also image the cells as they split. A particularly powerful advantage of doing both processes on the same microscope is that, ordinarily, the red proteins get diluted when the cell splits. Using the new microscope, the signal can be 'topped up' every generation, so the cells can be traced over much longer periods of time. In addition, because the method for imaging the cells in this microscope (known as light-sheet fluorescence microscopy) is particularly kind to cells (it uses very low light levels so that the cells do not get exposed to too much light) it is very suitable for studying embryos which are very sensitive to light and other perturbations.
Ultimately this microscope will be used for other applications outside of embryology as well. For example, the same system can be used to perform super-resolution imaging, allowing it to see beyond the so-called 'diffraction limit' which prevents microscopes from seeing very small things like viruses. It can be used to track immune cells as they fight off an infection, to quantify blood flow, and investigate how cancer invades the body. The whole system was designed to work as an add-on to a normal microscope, letting scientists work with the kinds of tools they are familiar with, and probably already have in their labs. Finally, because we are strong believers in open access to science, all the plans, software and data will be released for anyone to use.
Technical Summary
We propose development of a unique light-sheet microscope tailored specifically for the needs of Primed Conversion, which is a technique for changing a green photoconvertible protein into a red one with high spatial selectivity and low phototoxicity. While this ability to label an individual cell in a cluster has great promise in cell lineage tracing for embryology (along with many other fields), its adoption has been hampered by a lack of microscopes that can selectively label and image the developing embryo. This proposed system will function as an add-on to a conventional microscope, allowing researchers to maintain their existing sample mounting and culturing protocols, while integrating a highly optimized light-sheet fluorescence illumination modality and the ability to perform Primed Conversion with high three-dimensional resolution.
The project will focus on the construction and characterization of the instrument, as well as its use in embryology. All of the mechanical and optical design work has already been performed, and both the theoretical imaging and Primed Conversion resolutions are below one micron. After the instrument is constructed, it will be characterized using fluorescent nanospheres, as well as HeLa expressing H2B-pr-mEosFP (a photoconvertible protein). A major capability of the instrument will then be developed, that of 'dilution-unlimited' labelling. Unlike in normal labelling for lineage tracing, in which the label gets diluted as the cells divide (consequently reducing the signal to the point where it is lost), this system can photoconvert new proteins in every generation, thus boosting the signal and ensuring that it is not lost. This allows the lineage of a single cell to be traced through arbitrarily-many generations. Once all characterizations are complete and the instrument is ready for use, it will be tested on mouse embryos ordinarily discarded as a part of existing research activities.
The project will focus on the construction and characterization of the instrument, as well as its use in embryology. All of the mechanical and optical design work has already been performed, and both the theoretical imaging and Primed Conversion resolutions are below one micron. After the instrument is constructed, it will be characterized using fluorescent nanospheres, as well as HeLa expressing H2B-pr-mEosFP (a photoconvertible protein). A major capability of the instrument will then be developed, that of 'dilution-unlimited' labelling. Unlike in normal labelling for lineage tracing, in which the label gets diluted as the cells divide (consequently reducing the signal to the point where it is lost), this system can photoconvert new proteins in every generation, thus boosting the signal and ensuring that it is not lost. This allows the lineage of a single cell to be traced through arbitrarily-many generations. Once all characterizations are complete and the instrument is ready for use, it will be tested on mouse embryos ordinarily discarded as a part of existing research activities.
Planned Impact
Aside from the academic beneficiaries of this research, this research will also provide tangible benefits to industry and society. From an industrial perspective, one of the major difficulties in high-tech manufacturing is hiring well-trained workers who are experienced in precision work (such as the alignment of an optical system). This project directly provides this kind of training, as project students in the Department of Bioengineering will take small aspects of its construction under the supervision of the Postdoctoral Research Associate. It also supports the development of programmers in the same way; particularly programmers who are experienced in programming high-performance hardware, which is a niche skill and subject to constraints which are not encountered by the vast majority of software engineers. Training is also supported by the Rowlands lab policy of supporting short visits by external researchers who wish to learn how to build the microscope, some of the intricacies of using it, talk to the people who developed it and so on. Further industrial benefit comes from the availability of the system to other users; interested external users can apply to access the microscope to image their samples, as well as consulting with the researchers who built it. This is particularly suitable for small--to-medium enterprises who may not be able to afford a microscope with these capabilities; measurements taken using primed OPM (or even just normal OPM imaging) help support these companies to the benefit of the whole UK economy.
From the perspective of society, the research opens up interesting questions about how a single unthinking cell can turn into a person. Importantly, it does so in a very visual manner, which helps drive societal engagement. The images and videos produced during this project will be used both for artistic purposes, and to produce media intended for public consumption, with the goal of sharing our discoveries and excitement with a wider community. In this way artists, presenters, government officials and the whole general public can benefit from the resources produced. Finally, because the work studies the development process, it indirectly supports studies into reproductive disorders and developmental abnormalities. In the long term, we anticipate studies supported by this and similar instruments to be incredibly beneficial for couples struggling to have children, people with developmental disorders, and the general population as well.
From the perspective of society, the research opens up interesting questions about how a single unthinking cell can turn into a person. Importantly, it does so in a very visual manner, which helps drive societal engagement. The images and videos produced during this project will be used both for artistic purposes, and to produce media intended for public consumption, with the goal of sharing our discoveries and excitement with a wider community. In this way artists, presenters, government officials and the whole general public can benefit from the resources produced. Finally, because the work studies the development process, it indirectly supports studies into reproductive disorders and developmental abnormalities. In the long term, we anticipate studies supported by this and similar instruments to be incredibly beneficial for couples struggling to have children, people with developmental disorders, and the general population as well.
Publications
Bezer JH
(2020)
Elastic Deformation of Soft Tissue-Mimicking Materials Using a Single Microbubble and Acoustic Radiation Force.
in Ultrasound in medicine & biology
Boualam A
(2021)
Method for assessing the spatiotemporal resolution of structured illumination microscopy (SIM)
in Biomedical Optics Express
Fang C
(2021)
Editorial: Mechanisms of Fluorescent Proteins.
in Frontiers in molecular biosciences
Howe GA
(2023)
Tailored photoacoustic apertures with superimposed optical holograms.
in Biomedical optics express
Sesen M
(2021)
Thermally-actuated microfluidic membrane valve for point-of-care applications
in Microsystems & Nanoengineering
Whiteley I
(2023)
DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
in Biomedical Optics Express
Wright N
(2023)
mtFRC: depth-dependent resolution quantification of image features in 3D fluorescence microscopy.
in Bioinformatics advances
Description | Despite some serious challenges, the instrument has been constructed and aligned, and is able to take 3D image stacks. Currently the system is able to steer two focussed laser beams to any location within a small 3D volume, for use in primed conversion illumination, and software for all components has been created, barring the "infinite lineage tracing" code which is being written. The project will be taken forward by a PhD student for completion as part of their thesis, who will make further refinements for use in cancer tissue mapping and neurobiology. |
Exploitation Route | The instrument will form the basis of a PhD project to explore novel contrast mechanisms in Oblique Plane Microscopy, and the primed conversion aspect of the instrument can also be used separately (without the OPM imaging) for testing of new primed-convertible proteins. Once fully complete, the system is expected to form part of the Department of Bioengineering's microscopy suite (available for use by anyone), and work is almost complete upgrading the system to perform high-throughput spontaneous Raman mapping of tissue samples. Work is also progressing on using the system for neurobiological studies of flies. |
Sectors | Agriculture Food and Drink Chemicals Education Environment Healthcare Culture Heritage Museums and Collections Pharmaceuticals and Medical Biotechnology |
Description | After establishing that there is limited freedom to operate if we patent this instrument, we have decided to open-source all the design and characterization data for anyone to use. Additionally, we have opened up the use of the instrument to anyone interested in trying it. |
First Year Of Impact | 2023 |
Sector | Healthcare,Other |
Impact Types | Societal Economic |
Description | Cancer Led Optical Ultrasound Detection |
Amount | £99,998 (GBP) |
Organisation | Cancer Research UK |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 08/2022 |
End | 08/2023 |
Description | DORMOUSE: Detection Of Reflected Microscopic Optical UltraSound Emission |
Amount | £60,000 (GBP) |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 09/2021 |
End | 09/2025 |
Description | Deep Tissue Short-Wave Infrared Multiphoton Microscopy |
Amount | $1,000,000 (USD) |
Organisation | Chan Zuckerberg Initiative |
Sector | Private |
Country | United States |
Start | 01/2021 |
End | 06/2023 |
Description | Development of a portable, low-cost Raman spectrometer prototype for skin cancer diagnosis |
Amount | £4,200 (GBP) |
Funding ID | IES\R2\222231 |
Organisation | The Royal Society |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 11/2022 |
End | 10/2023 |
Description | Employing Raman in the Short-wave Infrared |
Amount | $2,200,000 (USD) |
Funding ID | DTI2-0000000206 |
Organisation | Chan Zuckerberg Initiative |
Sector | Private |
Country | United States |
Start | 03/2024 |
End | 02/2028 |
Description | Megapixel Ultrasound Scanners for Deep Tissue Cellular Imaging |
Amount | $1,000,000 (USD) |
Organisation | Chan Zuckerberg Initiative |
Sector | Private |
Country | United States |
Start | 01/2021 |
End | 06/2023 |
Description | Single Shot Spectroscopy Seeing Sensory Stimulation |
Amount | £38,775 (GBP) |
Organisation | Biotechnology and Biological Sciences Research Council (BBSRC) |
Sector | Public |
Country | United Kingdom |
Start | 02/2024 |
End | 06/2024 |
Description | The Computerized Chemist |
Amount | £60,000 (GBP) |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 09/2021 |
End | 09/2025 |
Title | Enhanced axial resolution temporal focusing microscope |
Description | Temporal focusing enables wide-field illumination with axial resolution through a single microscope objective. Because the axial resolution relies on second order dispersion it rarely achieves similar results to point-scanning methods. The new upgrade overcomes this issue by using a Diffractive Optical Element (DOE) to increase the dispersion by a factor of 11. |
Type Of Material | Improvements to research infrastructure |
Year Produced | 2024 |
Provided To Others? | Yes |
Impact | None yet |
Title | Raman OPM |
Description | Oblique plane microscopy is a method of performing light-sheet imaging (a photon-efficient illumination technique) whereby the sample is illuminated from the microscope objective by a tilted, focussed laser beam. The resulting signal from the sample is imaged by a novel arrangement of microscope objectives. In Raman-OPM, instead of exciting fluorescence in the sample, the system images uses a high-power narrow-bandwidth laser and images the resulting wavelength-shifted (Raman scattered) light. Raman scattering provides information on the chemical composition of a sample, and can be used in biomedical applications to assess whether a cell is a tumour cell or not, for example. The main advantage of Raman-OPM is photon efficiency. Normally Raman scattering is a very weak effect - most photons pass through the sample unchanged. In a light sheet geometry, these photons are 're-used' and can undergo scattering in the region behind the focus, increasing throughput and ultimately improving imaging speed while minimizing photodamage. OPM is merely a very convenient means of performing light-sheet microscopy - the same objective is used to excite and image the sample, and it can be mounted on a conventional, familiar microscope frame. |
Type Of Material | Improvements to research infrastructure |
Year Produced | 2022 |
Provided To Others? | No |
Impact | Preprint to be filed imminently, followed by submission to Nature Methods. |
Title | Parameter-free estimation of the achievable optical penetration depth in a variety of sample types. |
Description | The technique uses a single focal stack to estimate the smallest observable features at each plane and then construct a map of imaging depth vs maximum resolution. |
Type Of Material | Data analysis technique |
Year Produced | 2024 |
Provided To Others? | Yes |
Impact | None yet |
Title | Temporal analysis for super-resolution imaging |
Description | A method for analysing the temporal resolution of an imaging technique, particularly a super-resolution imaging technique such as Structured Illumination Microscopy. The method effectively performs a Fourier analysis in the time domain, modulating the average intensity of the image at a certain rate and assessing whether the imaging system is able to resolve it. In this way, it is possible to assess whether an imaging technique can actually resolve the temporal frequencies claimed, as opposed to crude extrapolation based on factors like camera frame rate. |
Type Of Material | Data analysis technique |
Year Produced | 2020 |
Provided To Others? | Yes |
Impact | Publication of a paper describing the technique |
URL | https://www.imperial.ac.uk/rowlands-lab/resources/ |
Description | High-speed fluorescence voltage sensors |
Organisation | Imperial College London |
Department | Faculty of Medicine |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | Development of a novel high-speed microscope for recording high-speed information from a live mouse brain |
Collaborator Contribution | Biological support - provision of GEVI-labelled mice, neurobiology advice, brain slicing expertise |
Impact | Invited talk given by my PhD student |
Start Year | 2020 |
Description | Low-cost Raman imaging for resource-constrained environments |
Organisation | Federal University of São Francisco Valley |
Country | Brazil |
Sector | Academic/University |
PI Contribution | This research program aims to develop a low-cost Raman spectrometer for use in countries such as Brazil which don't have easy access to high-performance analytical tools. We are developing the instrumentation, software and analytical routines needed to use the instrument effectively. |
Collaborator Contribution | The partners bring real-world experience of working in a resource-constrained environment, access to medical and agricultural applications and guidance on what would actually have an impact on their community. |
Impact | Collaborators were awarded a grant by the Brazilian government to continue the collaboration, spend time at Imperial and ultimately learn the skills to develop these spectrometers themselves. |
Start Year | 2023 |
Description | Mouse glioblastoma xenografts - Raman imaging |
Organisation | Imperial College London |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | This collaboration is at an early stage, but it emerged from the Raman oblique-plane microscopy work that was carried out as a backup for if the light-sheet illumination for cell identification didn't go according to plan. Once it became clear that the prototype was able to measure several Raman spectra simultaneously, I reached out to Dr Syed to see if it could be used to map her glioblastoma animal models. We have submitted a number of joint PhD proposals together; my lab is offering the Raman imaging technology (OPM-Raman and point-scanning instrumentation). |
Collaborator Contribution | As mentioned above, this collaboration is at the early stages but Dr Syed is contributing biological expertise and access to mouse xenografts of human glioblastomas. |
Impact | Applications for PhD studentships; currently two have been rejected, one is outstanding. The collaboration is multidisciplinary, combining Raman instrumentation and mouse xenograft models. |
Start Year | 2021 |
Description | Multiplexed fluorescence imaging |
Organisation | Imperial College London |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | We provide the optical imaging technology to spectroscopically distinguish many fluorophores within a sample; the technology is derived from a Raman OPM design |
Collaborator Contribution | The Higgins lab (Claire Higgins, Leah Redmond) are staining samples using many quantum dots, reporting the distribution of many different cell types in a skin sample. We can use these samples to test our microscope and demonstrate utility. |
Impact | Work currently ongoing. |
Start Year | 2022 |
Description | Organoid metabolic imaging with ICR |
Organisation | Institute of Cancer Research UK |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | We provide imaging hardware, analytical support, and guidance on image interpretation |
Collaborator Contribution | ICR provides samples, guidance on experimental design and help interpreting the results |
Impact | The collaboration has lead to a PhD studentship being awarded between my group, the Pantazis lab and the Maier lab. The student is expected to start in October. |
Start Year | 2022 |
Description | Primed conversion microscopy |
Organisation | Imperial College London |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | Development and construction of the optical design. We have designed a custom oblique plane microscope that can both image and photoconvert proteins at arbitrary locations in a sample volume. |
Collaborator Contribution | Provision of biological support - fluorescently-labelled organisms, fluorescent proteins, animal handling. |
Impact | We are in the process of preparing a high-profile paper on our joint work. |
Start Year | 2020 |
Description | Zebrafish imaging |
Organisation | Imperial College London |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | We developed a hyperspectral Raman microscope for label-free tissue imaging, and provide the expertise to maintain and use it. |
Collaborator Contribution | The collaborators provide live zebrafish samples along with the expertise to interpret the recorded data. |
Impact | Preprint released - currently submitted to PNAS. |
Start Year | 2022 |
Title | Common-Path Interferometer |
Description | The invention is a common-path interferometer which can be reconfigured (into multiple different interference patterns and phases) using a single galvanometric mirror. The design is photon-efficient, achromatic and able to be reconfigured within a millisecond. |
IP Reference | Not yet assigned |
Protection | Patent / Patent application |
Year Protection Granted | |
Licensed | No |
Impact | NDAs have been signed with Nikon and Olympus, and Zeiss is in progress. Olympus has expressed an informal interest in licensing the technology. |
Title | Hyperspectral OPM design |
Description | CAD model and alignment details for a hyperspectral Raman microscope |
Type Of Technology | Systems, Materials & Instrumental Engineering |
Year Produced | 2023 |
Open Source License? | Yes |
Impact | None yet |
Title | Single-moving-part Structured Illumination Microscope design |
Description | The design implements a SIM instrument with a single low-cost moving part, enabling high-speed super-resolution imaging over large fields of view. |
Type Of Technology | Systems, Materials & Instrumental Engineering |
Year Produced | 2024 |
Impact | Released at the same time as the pre-print |
URL | https://www.biorxiv.org/content/10.1101/2024.02.29.582785v1 |