Unveiling the molecular mechanisms to modulate peroxisome dynamics and abundance for improvement of cell performance

Lead Research Organisation: University of Exeter
Department Name: Biosciences

Abstract

One of the hallmarks of eukaryotic cells is the presence of membrane-bound compartments (organelles), which create different optimised environments to promote various metabolic reactions required to sustain life. To adapt to the changing physiological requirements of a cell or organism, organelles have to constantly adjust their number, shape, position, and metabolic functions accordingly. This requires dynamic processes which modulate organelle abundance by organelle formation (biogenesis), degradation (autophagy), or inheritance (cell division). Peroxisomes are multifunctional subcellular organelles that are essential for human health and development. Vital, protective roles of peroxisomes in lipid metabolism, signalling, the combat of oxidative stress and ageing have emerged recently. Our work has revealed that peroxisomes are extremely dynamic and can form from pre-existing organelles in a multistep process which requires remodelling of the peroxisomal membrane, the formation of tubular membrane extensions which subsequently constrict and divide into several new peroxisomes. Defects in peroxisome dynamics and multiplication have been linked to age related disorders involving neurodegeneration, loss of sight and deafness. Despite their fundamental importance to cell physiology, the mechanisms that mediate and regulate peroxisome membrane dynamics and abundance in humans are poorly understood and a biophysical model is missing. Understanding these mechanisms is not only important for comprehending fundamental physiological processes but also for understanding pathogenic processes in disease etiology. The overall aim of this project is to acquire novel insights into the mechanism and regulation of peroxisome abundance, membrane dynamics and organelle cooperation in normal and disease conditions.
In this research project, we will (1) assess the role of key proteins in peroxisome division to unveil the molecular mechanisms modulating peroxisome abundance, (2) apply biophysical approaches to investigate protein-lipid interaction and membrane remodelling, (3) identify mechanisms to modulate expression of key proteins and peroxisome dynamics for improvement of cell performance, and (4) develop a biophysical/mathematical model to understand and predict peroxisome dynamics in health and disease conditions.
In summary, in this interdisciplinary project we will combine unique complementary expertise in organelle-biology and organelle-based disorders with biophysical and mathematical approaches as well as novel tools and models in human cell biology. We will apply molecular cell biology, biophysical, biochemical and screening approaches, mathematical modelling and cutting edge imaging techniques to reveal the molecular mechanisms and pathways that mediate and regulate organelle membrane dynamics and organelle abundance. Specifically, this research project will improve our understanding of organelle dynamics/abundance and its impact on healthy ageing and common, degenerative disorders. We will generate new tools and models for assessing and modulating organelle dynamics, which may help to improve cell performance. Understanding how to modulate organelle dynamics and abundance and to use the protective functions of organelles will be of significant biological and medical importance. It may contribute to the development of new therapeutic approaches in healthy ageing and age-related disorders.

Technical Summary

In this project we will address fundamental open questions related to the molecular mechanisms and pathways that mediate and regulate organelle dynamics and abundance. The overall aim of this project is to acquire novel insights into the mechanism and regulation of peroxisome abundance, membrane dynamics and organelle cooperation in normal and disease conditions. Peroxisomes have vital, protective roles in lipid metabolism, signalling, and the combat of oxidative stress, thus influencing developmental and ageing processes. We will now apply novel tools and cellular models to assess and modulate organelle dynamics and abundance, which may improve cell performance in health and disease.
In this project we will (1) combine molecular cell biology, biochemical and microscopic approaches to determine the molecular mechanisms modulating peroxisome membrane dynamics and abundance in humans. We will (2) apply biophysical approaches to investigate membrane remodelling and lipid interaction of key proteins. Furthermore, we will (3) combine screening approaches with physiological studies to identify mechanisms to modulate expression of key proteins and peroxisome dynamics for improvement of cell performance, and (4) apply mathematical and computational modelling to develop a biophysical/mathematical model to understand and predict peroxisome dynamics in health and disease conditions.
This interdisciplinary project applies molecular cell biology, biophysical, biochemical and screening approaches, mathematic modelling and cutting edge imaging techniques to reveal the molecular mechanisms and pathways that mediate and regulate organelle membrane dynamics and organelle abundance. It will improve our understanding of organelle dynamics/abundance and its impact on healthy ageing and common, degenerative disorders.

Planned Impact

This project seeks to deliver ongoing national and international i) academic, ii) medical, iii) political, iv) economic and v) social impact from multi-disciplinary research by building knowledge around the link between organelle dynamics/abundance, cell performance and dysregulation which may result in disease (i, ii, iii, iv), and by improving understanding of associated proteins, their impact on healthy ageing, age-related disorders and diagnostics (i, ii, iv, v). By focusing on the topic of organelle dynamics and regulation of organelle abundance, its findings are highly relevant given the current importance of cellular redox balance and lipid/energy regulation in maintaining normal cellular homeostasis and in the ageing process. In the longer term, this new knowledge will also help inform on risk factors for the initiation and progression of common, age-related diseases such as obesity, diabetes, cardiovascular disease, neurodegeneration and cancer. The research proposed is novel and highly important to aid our understanding of how organelle dynamics and multiplication impact on normal and disease processes; it is therefore envisaged that this work will be beneficial for academics and clinicians as well as health professionals, charitable bodies and others engaged with health promotion by enhancing quality of life, health, wellbeing and healthy ageing. The work aims to understand fundamental processes in human cell biology, organelle biogenesis and cell physiology which have the potential to impact upon developments within both the biological and medical research communities and could enable the identification of new drugs and approaches to modulate organelle dynamics, which may help to improve cell performance in health and disease. This in turn has the potential to benefit understanding of healthy ageing, degenerative and other age-related diseases with the potential to be exploited in both the pharmacological and public health sectors. The fusion of multiple disciplines that constitutes this work will help to highlight to the general community the potential benefits of systems-led and inter- and multi-disciplinary research that UKRC are championing. The reason for this potential is that the mechanisms of organelle dynamics and regulation of abundance are poorly understood, but are essential for cellular viability and development of the organism. An additional outcome of this research will be the development of new tools and models for assessing and modulating organelle dynamics to improve cell performance in health and disease, which will be of benefit to the scientific community as a whole and impact on the development of both biological and medical science in this field.
Through cooperation with industry (Novatis, CH) this research has potential impact on the identification of drugs and the development of novel therapeutic approaches for healthy ageing and treatment of age-related disorders (of benefit to the UK and European pharmaceutical and health sectors) as well as in the diagnosis of pathophysiological conditions and disorders (public health sector). The project team and the University of Exeter's (UoE) Innovation, Impact and Business Team (UoE IIB) have established networks of industry contacts, and research findings will be formally reviewed annually, to explore and coordinate links with business and key project partners. The UoE has excellent links with the wider public with regular events with contributions from research staff. Researchers make regular school visits to explain their research and run events as part of National Science week. Programmes such as this and other outreach activities are critical for the long-term maintenance of the UK science base. This is also aided by the transfer of knowledge and skills between academia and industry. The PDRA and Technician will both receive full and relevant training. Several former PhD students are now working within the biotechnology or biomedical sector.

Publications

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Taatjes DJ (2019) Histochemistry and Cell Biology: 61 years and not tired at all. in Histochemistry and cell biology

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Schrader M (2019) Organelle interplay-peroxisome interactions in health and disease in Journal of Inherited Metabolic Disease

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Schrader M (2019) Zellweger UK - a glimmer of hope in SciTech Europa Quarterly

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Schrader M (2019) Peroxisomes - cellular team players in SciTech Europa Quarterly

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Silva BSC (2020) Maintaining social contacts: The physiological relevance of organelle interactions. in Biochimica et biophysica acta. Molecular cell research

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Passmore JB (2020) Mitochondrial fission factor (MFF) is a critical regulator of peroxisome maturation. in Biochimica et biophysica acta. Molecular cell research

 
Description We are addressing fundamental open questions related to the molecular mechanisms and pathways that mediate and regulate organelle dynamics and abundance. The overall aim of this project is to acquire novel insights into the mechanism and regulation of peroxisome abundance, membrane dynamics and organelle cooperation in normal and disease conditions. Peroxisomes have vital, protective roles in lipid metabolism, signalling, anti-viral defence and the combat of oxidative stress, thus influencing developmental and ageing processes. We are applying novel tools and cellular models to assess and modulate organelle dynamics and abundance, which may improve cell performance in health and disease.

We have so far produced a co-regulation map of the human proteome, which was able to capture relationships between proteins that do not physically interact or co-localize. This will enable the prediction and assignment of functions to uncharacterised human proteins. The co-regulation map can be explored at www.proteomeHD.net.

Exploring the map revealed unexpected co-regulation partners, namely the peroxisomal membrane protein PEX11ß with mitochondrial respiration factors.
This led to the identification of a novel interaction between two crucial cellular organelles in human cells - mitochondria and peroxisomes.

Peroxisomes and mitochondria in mammals are intimately linked and cooperate in the breakdown of fatty acids and cellular energy balance. Using live cell imaging we revealed that PEX11ß mediates the formation of membrane protrusions, which emanate from peroxisomes and interact with mitochondria. They likely function in the metabolic cooperation and crosstalk between both organelles, and may facilitate transfer of metabolites during mitochondrial energy (ATP) production.

We provided expertise in human cell biology and organelle dynamics to examine the mode of action of new fungicides in a cooperative approach at the University of Exeter to join the fight against plant pathogenic fungi. Our studies resulted in the identification of novel mono-alkyl chain lipophilic cations (MALCs) in protecting crops against Septoria tritici blotch in wheat and rice blast disease. We discovery that MALCs inhibit the activity of fungal mitochondria. Mitochondria are the cellular "power-house", required to provide the "fuel" for all essential processes in the pathogen. By inhibiting an essential pathway in mitochondria, MALCs cut down the cellular energy supply, which eventually kills the pathogen. A synthesised MALC named C18-SMe2+ showed unexpected additional modes of action. Firstly, C18-SMe2+ generated aggressive molecules inside the mitochondria, which targeted life-essential fungal proteins, and in turn initiated a "self-destruction" programme, which ultimately resulted in "cellular suicide" of the fungus.
Secondly, when applied to crop plants, C18-SMe2+ "alerted" the plant defence system, which prepared the crop for subsequent attack, thereby increasing the armoury of the plant against the intruder. Most importantly, the Exeter researchers demonstrated that C18-SMe2+ showed no toxicity to plants and is less toxic to aquatic organisms and human cells than existing fungicides used in the field today. The University has filed a patent (GB 1904744.8), in recognition of the potential of this novel chemistry in the perpetual fight against fungi.

We established MFF-deficient cells as a model system to study peroxisome dynamics. Defects in MFF (a fission protein) block the division of mitochondria and peroxisomes and result in highly elongated organelles unable to divide. Patients with MFF deficiency present with developmental and neurological abnormalities. The majority of studies into MFF-deficiency have focused on mitochondrial dysfunction, but the contribution of peroxisomal alterations to the pathophysiology is largely unknown. We have now shed light on peroxisome alterations and their contribution to the disease.

We revealed that MFF-deficiency impacts on the maturation of peroxisomes. Loss of MFF function results in an altered distribution of peroxisomal proteins and causes the accumulation of extremely long pre-peroxisomal membrane structures inside the cell, which have reduced import-competency for peroxisomal enzymes. Furthermore, we show that peroxisomes in MFF-deficient cells display alterations in peroxisomal redox state and intra-peroxisomal pH.

Previous studies have shown that the peroxisomes in MFF-deficiency are largely functional, leading to the general assumption that defects in peroxisomal dynamics and division results only in elongated peroxisomes, which are otherwise unaltered. We have now revealed in MFF-deficient cells that this is not the case.

Interestingly, we observed that the highly elongated peroxisomes in MFF-deficient cells are not fully static; their dynamics can be modulated, for example through the induction of organelle degradation (autophagic processes).

These experiments have provided us with new insights into the pathophysiology of MFF-deficiency and related disorders with impaired peroxisome plasticity. In peroxisomal disorders, we often see altered numbers, different shapes or even different distributions of peroxisomes in patient cells. We also developed a mathematical modelling approach to help understand this. Understanding why this happens and how to modulate peroxisome numbers or distribution can provide new possibilities to improve cell performance in those patients. This might also be relevant to age-related conditions like dementia, deafness and blindness, as peroxisomal dynamics are known to have important protective functions within sensory cells.

As outlined, how changes in peroxisome dynamics and number are mediated and regulated in humans is not fully understood. As deficiencies in peroxisome proliferation have been associated with a variety of disease states, including liver diseases and neurological dysfunction, as well as cellular aging, a clearer understanding of the mechanisms and signalling pathways that control peroxisome plasticity could allow for modulation of peroxisome abundance to improve cellular function in health and disease. We therefore developed and applied a cell-based peroxisome proliferation assay to investigate the ability of different stimuli to induce peroxisome proliferation. We determined that serum stimulation, long-chain fatty acid supplementation and TGFß (Transforming growth factor beta) application all increased peroxisome elongation, a prerequisite for proliferation.

Examination of mRNA levels during peroxisome proliferation suggested differential regulation of peroxisomal genes correlating with their cellular function. Specifically, we identified differential regulation and functions of the PEX11 isoforms PEX11a and PEX11ß in peroxisome dynamics. An initial map of putative regulatory motif sites in the respective gene promoters showed a difference between transcription factor binding sites in PEX11a and PEX11ß, suggesting that these genes may be regulated by distinct pathways.

We identified a functional SMAD2/3 binding site in the promoter of PEX11ß, which suggests a novel link between the TGFß signalling pathway and the induction of peroxisome proliferation, potentially via PEX11ß expression, providing new insights into the regulation of peroxisome dynamics in humans.

To mitigate the impact of Covid on our research activities, we performed bioinformatics analyses and combined them with molecular cell biology to reveal the ?rst comprehensive inventory of zebrafish (Danio rerio) peroxisomal proteins, which we systematically compared with those of human peroxisomes.

Through bioinformatics analysis of peroxisomal targeting signals we revealed novel candidate peroxisomal proteins in zebrafish, and revealed similarities and differences in comparison to the human peroxisomal protein inventory and associated metabolic pathways. Our ?ndings con?rm the suitability of zebra?sh as a vertebrate model for peroxisome research and open possibilities for the study of novel peroxisomal candidate proteins in zebra?sh and humans.

Peroxisome membrane dynamics and division are essential to adapt the peroxisomal compartment to cellular needs. The peroxisomal membrane protein PEX11ß, and the tail-anchored adaptor proteins FIS1 (mitochondrial fission protein 1) and MFF (mitochondrial fission factor), which recruit the fission GTPase DRP1 (dynamin-related protein 1) to both peroxisomes and mitochondria, are key factors of peroxisomal division. The current model suggests MFF is essential for peroxisome division, whereas the role of FIS1 is unclear.

We now discovered that PEX11ß can promote peroxisome division in the absence of MFF in a DRP1-dependent manner. We show that PEX11ß requires FIS1 to induce peroxisome division in the absence of MFF, and that MFF can restore peroxisome division in PEX11ß-deficient patient fibroblasts. Interestingly, targeting of PEX11ß to mitochondria induces mitochondrial division revealing the potential for PEX11ß to modulate mitochondrial dynamics. Our findings indicate that MFF and FIS1 can act independently in peroxisome division, and suggest the existence of an alternative, MFF-independent pathway in peroxisome division which depends on PEX11ß and FIS1.

Our observations suggest that modulation of MFF or PEX11ß protein levels may represent a therapeutic option to overcome the defects in peroxisome dynamics. Pharmacological agents that up-regulate MFF or PEX11ß may therefore be of therapeutic value to restore peroxisome dynamics in certain disease conditions.

To identify those molecular compounds, we used CRISPR/Cas technology and established a reporter cell line expressing a fusion of nano-Luciferase and PEX11ß under control of the endogenous promoter. The cell line also stably expresses Renilla Luciferase as a control to allow ratio measurements based on luminescence. The reporter cell line is used in cooperation with our industrial partner Novartis to establish assays to perform small and large scale compound screens to identify compounds which modulate the expression of human PEX11ß. This work has important implications for the fundamental understanding of how peroxisomal proteins are regulated and may reveal the therapeutic potential of modulating peroxisomal protein expression to improve cell performance (assay evaluation is ongoing as delayed due to the impact of Covid on our research activities; a manuscript about the generation of those reporter cell lines and their application is in press).
Exploitation Route The project has high potential to contribute to therapeutic approaches, not only for the treatment of organelle-based disorders but also for pathological conditions associated with oxidative stress, cellular energy regulation, anti-viral defence and cellular ageing.
Sectors Communities and Social Services/Policy,Education,Healthcare,Pharmaceuticals and Medical Biotechnology

URL http://www.exeter.ac.uk/news/research/title_763295_en.html
 
Description Our findings have so far contributed to a better understanding of peroxisome-mitochondria interplay and co-regulation of human proteins which is medically relevant. Our findings have been used by other scientists to identify new proteins within the human proteome, which are co-regulated. This resulted in the association of new functions with human proteins and greatly supported our concept of the peroxisome-mitochondria connection which is of biological and medical importance. Our findings allow the identification of new relationships between human proteins and thus, the identification of new protein functions. Our findings have led to the development of tools to identify co-regulation of human proteins (co-regulation map). Our findings have supported diagnostics of peroxisome-organelle based disorders (e.g. peroxisome-mitochondria). Our studies have contributed to the identification of a new chemistry and mode of action to protect our crops from fungal disease. The University has filed a patent (GB 1904744.8), in recognition of the potential of this novel chemistry in our perpetual fight against fungi. Our findings have provided new insights into the pathophysiology of MFF-deficiency and related disorders with impaired peroxisome plasticity. In peroxisomal disorders, we often see altered numbers, different shapes or even different distributions of peroxisomes in patient cells. We also developed a mathematical modelling approach to help understand this. Understanding why this happens and how to modulate peroxisome numbers or distribution can provide new possibilities to improve cell performance in those patients. This might also be relevant to age-related conditions like dementia, deafness and blindness, as peroxisomal dynamics are known to have important protective functions within sensory cells. Our findings have led to the identification of stimuli and new signalling pathways which regulate and modulate peroxisome proliferation in humans. As deficiencies in peroxisome proliferation have been associated with a variety of disease states, including liver diseases and neurological dysfunction, as well as cellular aging, a clearer understanding of the mechanisms and signalling pathways that control peroxisome plasticity could allow for modulation of peroxisome abundance to improve cellular function in health and disease. Our recent observations also suggest that modulation of MFF or PEX11ß protein levels may represent a therapeutic option to overcome the defects in peroxisome dynamics. Pharmacological agents that up-regulate MFF or PEX11ß may therefore be of therapeutic value to restore peroxisome dynamics in certain disease conditions.
Sector Education,Healthcare
Impact Types Cultural,Societal

 
Description IB syllabus
Geographic Reach Multiple continents/international 
Policy Influence Type Contribution to new or Improved professional practice
 
Title Cell-based peroxisome proliferation assay 
Description We developed a cell-based assay which allows to identify stimuli and mechanisms which modulate peroxisome dynamics and proliferation in human cells. 
Type Of Material Model of mechanisms or symptoms - human 
Year Produced 2020 
Provided To Others? Yes  
Impact The cell-based assay has been successfully applied to identify novel stimuli and signalling pathways which modulate peroxisome proliferation in human cells. This has increased our understanding of this process in humans which is still unclear. 
URL https://pubmed.ncbi.nlm.nih.gov/33195217/
 
Title Reporter cell line 
Description We created a dual reporter cell line for luminescence -based reporter assays to identify components which will modulate peroxisome abundance in human cells. 
Type Of Material Cell line 
Year Produced 2019 
Provided To Others? No  
Impact The reporter cell line will be used in cooperation with our industry partner to perform a large scale compound screen to identify novel compound to modulate organelle/peroxisome abundance. This will be beneficial for the development of therapies to treat organelle/peroxisome-based disorders (including age-related disorders, neurodegeneration). 
 
Title Co-regulation map of the human proteome 
Description We supported our cooperation partner in generating/validating a machine learning algorithm to reveal functional associations between co-regulated human proteins. 
Type Of Material Computer model/algorithm 
Year Produced 2019 
Provided To Others? Yes  
Impact The new co-regulation map identifies new relationships between human proteins, and thereby enables functional annotation of human proteins. Co-regulation was able to capture relationships between proteins that do not physically interact or colocalize. Based on co-regulation data, we discovered a new mechanism of organelle interaction/interface between peroxisomes and mitochondria in human cells mediated by PEX11ß with mitochondrial respiration factors. 
URL http://www.proteomeHD.net
 
Description Co-regulation map 
Organisation Technical University Berlin
Country Germany 
Sector Academic/University 
PI Contribution We provided experimental evidence/proof-of-principle for a new machine learning algorithm to reveal-regulated proteins in the human proteome.
Collaborator Contribution The partner shared unpublished information and research data and provided access to a novel prediction tool (co-regulation map). Furthermore, protein/organelle samples were analysed by the partner.
Impact The cooperation resulted in a cooperative high-impact publication in Nature Biotechnology and in a new tool/algorithm, a co-regulation map for human proteins, which is publicly available.
Start Year 2018
 
Description Organelle contacts and oxidative stress 
Organisation University of Leuven
Country Belgium 
Sector Academic/University 
PI Contribution Analysis of the impact of oxidative stress on membrane contacts sites/organelle cooperation in human cells using molecular cell biology and ultrastructural studies/quantitative EM.
Collaborator Contribution The partner generated samples using a sophisticated cell model generated by the partner, which allows generation of H202/oxidative stress in different cellular compartments.
Impact The collaboration generated data for publication and upcoming grant proposals. It contributed to skills training and closer cooperation with the partner. This is a multi-disciplinary cooperation which combines biochemical and cell biological/ultrastructural approaches.
Start Year 2021
 
Description Targeting analysis of peroxisomal proteins 
Organisation Medical University of Vienna
Department Center for Brain Research
Country Austria 
Sector Academic/University 
PI Contribution We have performed bioinformatics analyses and combined them with molecular cell biology to provide a first comprehensive inventory of peroxisomal proteins and their metabolic pathways in the zebrafish Danio rerio.
Collaborator Contribution The partner has performed a comprehensive bioinformatics analysis of the peroxisomal targeting signals and experimental verification of peroxisomal targeting.
Impact A manuscript with the combined data from both partners has been published (in press). Another manuscript is in preparation. The collaboration is multidisciplinary as it combines bioinformatics with molecular cell biology.
Start Year 2020
 
Description Biosciences Research Conference 2022 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Professional Practitioners
Results and Impact Our research team participated in the Biosciences Research Conference (28-29 June 20220 at the University. The conference brought together the diverse and dynamic research that is done in the Biosciences department. BBSRC-funded researchers were selected for an oral presentation and talked about the ongoing research in our lab or presented posters. A BBSRC-funded PDRA from our team was also a member of the organising committee.
This sparked questions and discussions afterwards, informed others about our BBSRC-funded research and resulted in requests for more information or collaboration. It supported networking activities and contributed to the skills training of the BBSRC-funded team members (e.g., organisation, oral and poster presentation, communication).
Year(s) Of Engagement Activity 2022
 
Description Chatting with school students about science 
Form Of Engagement Activity Engagement focused website, blog or social media channel
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Schools
Results and Impact Participation in the MRC Medical Research Zone on the 'I'm a Scientist' platform. 'I'm a Scientist' allows school students to meet scientists through live text-based chats. The students can ask the scientists anything, about their research, science in general, career, as well as hobbies and favourite food, so that they discover that scientists are 'real' human beings and that live sciences are fascinating and worthwhile to engage with. This sparked questions about science/UKRI funded research, generated interest in scientific research and careers in life sciences.
Year(s) Of Engagement Activity 2020
 
Description EU ITN presentation 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact Presentation about "Organelle Dynamics in Health and Disease" at an EU ITN training event about organelles in health and disease. The presentation sparked questions and discussions afterwards and contributed to the training of an international cohort of PhD students working on organelle biology. The event informed about recent developments in the field and about our BBSRC funded research. The presentation and discussion was very well received and contributed to the overall success of the training event, which was highly rated by the participants afterwards.
Year(s) Of Engagement Activity 2020
 
Description First Person Interview 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Professional Practitioners
Results and Impact Tina A. Schrader and Ruth Carmichael, joint first authors of a research paper published in J Cell Sci, were interviewed by the journal. The interview was afterwards published by the journal. This increased interest in our research, sparked question and discussions.
Year(s) Of Engagement Activity 2022
URL https://journals.biologists.com/jcs/article/135/13/jcs260359/275956/First-person-Tina-Angelika-Schra...
 
Description MFF deficiency 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Public/other audiences
Results and Impact Press release to inform and increase awareness of new discoveries in molecular cell biology with link to biomedicine/human disease with respect to organelle plasticity and defects in organelle multiplication. Our study has shed new light on how a group of novel organelle-based disorders affect cells. It sparked questions and discussions, increased awareness and interest.
Year(s) Of Engagement Activity 2020
URL https://lifesciences.exeter.ac.uk/news/articles/newresearchgivesinsightsi.html
 
Description Organelle division 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Media (as a channel to the public)
Results and Impact Press release to inform and increase awareness of new discoveries in molecular cell biology with link to biomedicine/human disease with respect to organelle dynamics and defects in organelle division and multiplication. Our study has revealed an alternative pathway for organelle/peroxisome division, which may be of therapeutic benefit. It sparked questions and discussions, increased awareness and interest.
Year(s) Of Engagement Activity 2022
URL http://www.exeter.ac.uk/research/news/articles/newresearchgivesinsightsi.html
 
Description Orientation workshop 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach Regional
Primary Audience Postgraduate students
Results and Impact The workshop contained a presentation and discussion about tips & tricks for a good scientific presentation with focus on PhD students in a regional program and covered oral and poster presentations at workshops/conferences and during interview situations. This contributed to the skills training (presentation, communication, employability) of the participating PhD students. The workshop was very well received and sparked questions and discussions afterwards, with increased interest in similar activities.
Year(s) Of Engagement Activity 2020
 
Description Press release - fungal disease 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Media (as a channel to the public)
Results and Impact Press release to inform and increase awareness of new chemistry to protect crops against fungal pathogens by multiple modes of action of a lipophilic cation, which acts on fungal mitochondria. It sparked questions and discussions, increased awareness and interest. Aim is to seek partners/investors to take this development to the field and prove its usefulness under 'real agricultural conditions'. The long-term aim is to foster greater food security, in particular in developing nations.
Year(s) Of Engagement Activity 2020
URL http://www.exeter.ac.uk/news/research/title_784511_en.html
 
Description Press release - protein co-regulation map 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Public/other audiences
Results and Impact Press release to inform and increase awareness of new discoveries and tool in cell biology/bioinformatics with link to biomedicine/human disease with respect to co-regulation of human proteins and identification of protein functions. It sparked questions and discussions, increased awareness and interest.
Year(s) Of Engagement Activity 2019
URL http://www.exeter.ac.uk/research/newsandevents/news/title_763295_en.html
 
Description Research Highlight 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Professional Practitioners
Results and Impact Based on our published research article in J Cell Sci, a Research Highlight "A new pathway for peroxisome division" was published, which increased interest in our research on organelle dynamics and in our research group, and sparked questions and discussions.
Year(s) Of Engagement Activity 2022
URL https://journals.biologists.com/jcs/article/135/13/e135_e1303/275978/A-new-pathway-for-peroxisome-di...
 
Description Research presentation (Tuebingen) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact I was invited for an online presentation at the University of Tuebingen, Dept. of Biochemistry to talk about peroxisome-organelle interaction, dynamics and cooperation in health and disease. This sparked questions and discussions afterwards and resulted in an increased interest in the subject. It informed about our BBSRC-funded research activities, increased outreach and engagement.
Year(s) Of Engagement Activity 2021
 
Description Research presentation (Washington) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact I was invited to give an online presentation at the Dept. of Biology, The Catholic University of America, Washington DC, USA about peroxisome-organelle interplay and dynamics in health and disease. This sparked intensive questions and discussions afterwards, informed a broader audience about organelle cooperation and organelle dynamics in health and disease, increased interest in the subject area as well as in international cooperation.
Year(s) Of Engagement Activity 2021
 
Description Widening paricipation -work experience placement 2019 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Schools
Results and Impact Work experience placement week for yr 10 students from a local school; the pupils spend a week in the research team performing experiments related to molecular cell biology, organelle biology/peroxisomes, analysed data, discussed results and obtained insight into the day-to-day work of scientists, academics, experimental officers and students. Several research facilities in the Dept. were visited and the students took part in demonstrations. Overall, this generated increased interest in and understanding of Biosciences and science in general, sparked questions and discussions and supported decision-making for future careers.
Year(s) Of Engagement Activity 2019
 
Description Work experience/internship (school) 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Schools
Results and Impact A student from a local College performed a work experience/internship in my research group. Due to Covid-19 restrictions, the project was performed remotely with focus on bioinformatics analyses of membrane protein targeting to organelles. The student really enjoyed the project and engaged with UG and PG students at University as well as with academics. The internship contributed to the skills training of the student, who is interested in Biosciences/Medical Biosciences and will support his UK University application. It also informed about our BBSRC funded research in organelle biology and disease.
Year(s) Of Engagement Activity 2020
 
Description ZUK Charity activity 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Undergraduate students
Results and Impact A member of the Zellweger UK charity and parent/carer of a Zellweger patient informed UG/PG students and academic staff about the work and aims of the ZUK charity and the day-to-day life with a Zellweger patient. This patient-centred online session complemented learning activities on the underlying biological science and diagnostics. The session was very well received and sparked questions and discussions afterwards. It greatly increased awareness of organelle/peroxisome-based disorders and our BBSRC funded research.
Year(s) Of Engagement Activity 2020
URL https://www.zellweger.org.uk/
 
Description ZUK charity session 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Undergraduate students
Results and Impact A member of the Zellweger UK charity and parent/carer of a Zellweger patient informed UG/PG students and academic staff about the work and aims of the ZUK charity and the day-to-day life with a Zellweger patient. This patient-centred session complemented learning activities on the underlying biological science and diagnostics. The session was very well received and sparked questions and discussions afterwards. It greatly increased awareness of peroxisome-based disorders and our BBSRC funded research.
Year(s) Of Engagement Activity 2019
URL http://www.zellweger.org.uk
 
Description Zellweger Charity Event 2022 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Undergraduate students
Results and Impact A member of the Zellweger UK charity and parent/carer of a Zellweger patient informed UG/PG students and academic staff about the work and aims of the ZUK charity and the day-to-day life with a Zellweger patient. This patient-centred online session complemented learning activities on the underlying biological science and diagnostics. The session was very well received and sparked questions and discussions afterwards. It greatly increased awareness of organelle/peroxisome-based disorders and our BBSRC funded research.
Year(s) Of Engagement Activity 2022
URL https://www.zellweger.org.uk/
 
Description Zellweger UK Charity Family Conference 2019 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Patients, carers and/or patient groups
Results and Impact Family Meeting/Conference with patients and carers dealing with peroxisome biogenesis disorders/Zellweger Syndrome Disorders as well as researchers and national/international medical experts (USA, The Netherlands). Presentation about peroxisome biology, role in health and disease and peroxisome/organelle research in the UK sparked questions and discussions afterwards, and plans to increase awareness of PBDs (in the UK and internationally) were further developed.
Year(s) Of Engagement Activity 2019
URL http://www.zellweger.org.uk/