Events

Time: 2pm – 3pm (BST)

Professor Rhian Touyz from the University of Glasgow, and Editor-in-Chief of Clinical Science, will chair this hour-long webinar which will explore Angiotensin converting enzyme 2 (ACE2) – the major enzyme responsible for conversion of Ang II into Ang-(1-7), and receptor for severe acute respiratory syndrome (SARS)-coronavirus (CoV)-2, which causes Coronavirus Disease (COVID)-19.

The programme will cover the historical background and ACE2 discovery, and explore the enzymatic and non-enzymatic functions of ACE2. Other speakers include Professor Anthony Turner from the University of Leeds and Professor Michael Bader from The Max Delbrück Center for Molecular Medicine.

Time: 2-3pm

Professor Matt Dalby, recipient of the Biochemical Society’s Industry and Academic Collaboration Award 2020, will talk about the technology that is being developed towards use for providing osteoinductive cells for cell therapy and cell scale up.

This will be followed by Steve Swioklo, Senior Scientist at Atelerix, a biotechnology company, who provide tools that enable the shipment of cells and cellular therapies at room temperature, thus avoiding the need for cryo-logistics and the subsequent loss of viability, from the freeze-thaw cycle.

The course is aimed at anyone teaching or supporting teaching in bioscience at Higher Education, from early career to experienced lecturers, interested in embedding relevant technology in their practice to improve students’ learning. The course will be informed by evidence and will include case studies and online discussions among participants, who will be encouraged to share their experiences.

The course is composed of five modules:

• E-portfolios for evidencing professional practice
• Supporting assessment and feedback through digital technologies
• Online test: different approaches to enhance student learning
• Using your VLE to support teaching
• Making the most of the tools in your VLE

Discussions among participants and with lead educators will be central to the course, and delegates will have the opportunity to share their experiences by posting case studies outlining how they use technology in their teaching and what works best for them.

Completing this course will help colleagues working towards various levels of fellowship of the HEA.

Without a template, the biosynthesis of glycans heavily relies on the organisation of enzymes in the Golgi apparatus. In addition, glycan functions often feedback on important basic cell biological processes such as membrane trafficking and signalling. Therefore, understanding the interfaces between intracellular organisation and glycobiology is crucial to provide new tools and understanding for the functional investigation of glycans.

This scientific meeting will bring together glycoscientists with cell biologists to foster new ideas and collaborations between both disciplines. A range of topics from traditional cell and glycobiology through analytics and synthetic carbohydrate chemistry all the way to systems level studies will be explored at the event to encourage more joined-up thinking.

DNA Replication is one of the most fundamental processes in life. Every dividing cell has to duplicate its genome before cell division. Mistakes during DNA replication are a major cause of genomic instability that can lead to cancer development. With this in mind, research into the biochemistry of DNA replication is of high interest for many groups around the world and biotech companies.

The Biochemical Society invites you to submit an abstract for an oral or poster presentation to share your work on a variety of themes, which include:

• Origins of replication
• Origin firing
• Elongation and termination
• Replication and chromatin
• Replication and transcription
• Replication stress

This meeting will provide an excellent opportunity to network with colleagues working in this field. At this event, we will also be welcoming Dr Sara Priego Moreno to present her work as the recipient of the Biochemical Society’s Early Career Researcher 2020 award.

R for Biochemists 101 aims to equip early career researchers with the information, tools and techniques to use R. It is suited to beginners that want to use the programming software but have little or no experience.

The course will focus on getting data in R, manipulating and visualizing them using various methods. Each module will use a biochemical experiment and data as a starting point.

The course is divided in 5 modules:

• Draw a protein standard curve using base R and ggplot2
• Extracting data from objects
• Drawing an enzyme kinetics plot
• Customizing and reusing plots with R
• Getting your data into R for exploration

The estimated time of completion for each module is one hour, however, participants will be able to learn at their own pace and will benefit from the interaction with the course lead educator and other fellow participants. Dr Paul Brennan will reply to your comments and queries for five weeks. After this time, you’ll be able to still access the course, but the interaction with the course leader won’t be available.

Thiol redox reactions are implicated in a diverse range of physiological processes and are often dysregulated in human pathologies such as cancer, neurodegeneration and metabolic disorders. Low-molecular-weight (LMW) thiols play an essential role in maintaining the cellular redox homeostasis and exert important functions in cell growth, metabolism and detoxification pathways.

In the last decade, there have been significant advances in our understanding of redox biology, facilitated by the development of cutting-edge technologies and research tools. This conference will be one of the first to focus on the versatile family of LMW thiols in health and disease, a family which contains structurally and functionally diverse molecules with a range of evolutionary histories.

The programme will give attendees the chance to learn about the most recent developments on the role of LMW thiols in redox regulation, signalling, and health and disease from leading experts in the field, and provide networking opportunities to encourage new collaborative interactions between participants and further advance research in this field.

FREE for members

To communicate beyond the lab requires a different set of skills. In this online course ‘Introduction to Public Engagement and Science Policy’, we will explore how the molecular biosciences can contribute to UK policy, and share tools that can be used to engage the public effectively.

This course is ideal for early to late career bioscientists who wish to learn more about science policy and public engagement. Each module will be around 2 hours.

The course modules will cover:

• Introduction to science communication
• Science in policy-making – a guide to the UK landscape
• Public engagement activities
• Evaluation of impact

You will have access to the module for one year, and lead educators will reply to your comments in the first 6 weeks, so you’re encouraged to complete the course during this time.

The purpose of this training event is to familiarise participants with approaches and computational programmes to generate 3D models of proteins where no structural data is available. Additionally, an introduction to molecular docking will be given. An emphasis will be placed on critically evaluating the usefulness of models and modelling in general for solving scientific problems.

This hands-on course is aimed at early career scientists, such as PhD students and PostDocs, and established scientists who are interested in applying computational approaches to their research in the fields of protein science, molecular health, medicinal chemistry and structural biology.

Mutations in Leucine-Rich Repeat Kinase 2 (LRRK2) are the most common genetic cause of Parkinson’s disease (PD), responsible for up to 2-3% of all PD cases in the UK and up to 40% in some populations. Coupled with its clear genetic links to PD, LRRK2’s status as a complex, multi-domain kinase has led to this protein being flagged as one of the most promising drug targets for Parkinson’s disease.

The field is witnessing major advances in our understanding of the function of LRRK2 and its role in human disease and is the focus for this year’s biennial scientific meeting on LRRK2.

The conference programme will explore the genetic forms of PD, the LRRK2 gene and the LRRK2 protein, as well as the basic LRRK2 signalling mechanisms and physiological and pathological functions of LRRK2. In addition, non-neuronal LRRK2 signalling, particularly with respect to neuroinflammation and the immune system in PD, will be covered, as well as the role of LRRK2 in non-PD conditions.

We are welcoming abstracts for both oral communications and poster presentations, from both industry and academia and across all career stages. The meeting will be of particular interest to those working in biochemistry, neuroscience, biotechnology and pharmaceuticals.

From bacteria to eukaryotes, cells have evolved a remarkable battery of enzymes to deal with the mechanical and topological challenges presented by nucleic acid production, processing and maintenance. A clear view of the biology of the genetic material requires a molecular understanding of how these enzymes function. Such an understanding will enhance our ability to manipulate genome structure and gene expression.

The theme of this meeting revolves around the mechanisms of these enzymes, with particular emphasis on research that integrates structural, biochemical, biophysical and computational approaches. With recent technological advances in imaging (i.e., single-molecule and cryo-electron microscopies), we expect to witness a flourish of key biological systems to be characterised with unprecedented detail.

The meeting will cover many of the molecular mechanisms by which large macromolecular machines carry out a diverse range of nucleic acid processes including DNA replication and repair, gene transcription and regulation, RNA processing and splicing, translation, nucleic acids structures and chromatin structure and epigenetic mechanisms. The meeting will also explore new quantitative techniques as well as theoretical approaches.

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Collaborating societies

Kinases and pseudokinases fulfil allosteric, scaffolding, molecular switch and decoy roles in cell signalling. The recent attention on pseudokinases has shone a light on under-appreciated non-catalytic functions that can be mediated by kinases, raising the prospect that novel and specific therapeutics could target these functions.

2021 marks the 30th anniversary of the publication of the first protein kinase structure (Knighton et al, Science 1991). Much of our understanding of these diverse proteins has emanated from this structure, providing an important context for this meeting and a milestone to be celebrated.

This topic is the theme of the 88th Harden Conference, an event series unique to the Biochemical Society, providing residential research conferences covering a specialist topic. These events are widely recognised for their emphasis on free and open discussion to encourage the exchange of the latest data and a critical discussion of the technical challenges that these developments face.

Translation is an essential highly conserved process which is required for the synthesis of proteins in both prokaryotic and eukaryotic cells. This unique annual UK scientific meeting enable discussing the latest progress in this field and fostering collaborations between researchers.

This year’s meeting will cover a wide range of topics related to translation, including:

• mechanistic basis of regulation
• upstream signal transduction cascades
• genomic architecture
• ribosome structure and function
• structure of translation factors/complexes and regulatory factor
• genome-wide investigation of translation
• RNA/tRNA modifications and localisation

The conference is also an important forum for young researchers at PhD and postdoctoral levels, providing opportunities for to deliver oral and poster presentations to promote their research. As part of the programme, we will host a dedicated Early Career Researcher event to promote further networking amongst this group.

Ribosome profiling is still a relatively new technique. Although many people perform these types of experiments, there is still a small number of groups that have successfully published results and there are currently no standard analysis pipelines in the field.

This one-day workshop is aimed at PhD students and postdoctoral researchers and will provide an excellent training platform for scientists who are planning their ribosome profiling experiments, and those struggling with either wet lab or computational trouble shooting. It will offer a collaborative environment to share knowledge on many of the technical aspects of ribosome profiling, both practical and bioinformatic.

The course will combine short technical presentations with discussions and questions aimed to help both individuals planning or just starting experiments, and those that are in the middle of analysis and would like further support.

*Please note that delegates are required to bring their own laptops.

This three-day training event for early career researchers will focus on the function on biological membranes and on the biophysical techniques available to study their components in the context of biology and biotechnology. The event will comprise lectures, computer and laboratory-based practical sessions. Participants will leave the event with new knowledge and protocols that will allow them to use biophysical techniques for studying components of biological membranes in their research.

Topics include:

• High throughput membrane protein expression
• Solubilisation strategies
• Membrane protein purification
• Structural determination via circular dichroism, crystallography and EM
• Lipid nanoparticles and their analysis.
• Lipidomics via mass spectroscopy
• Biophysical analyses including NMR and neutron scattering.

This training event will be followed by the ‘European SMALP meeting 2020’.

The application of styrene-maleic acid (SMA) co-polymers to extract small discs of membrane, termed SMA lipid particles (SMALPs), has changed the established landscape of research in biological membranes. Membrane proteins play a vital role in cellular communication and the control of transport  across the membrane, making them key therapeutic targets for many human diseases. Their location within the membrane, tightly packed with so many different proteins and lipids has, until now, made them extremely challenging to study. By allowing membrane proteins to be purified and studied whilst maintaining their lipid environment, the SMALP methodology enables the study of membrane protein structure and function using techniques that were previously impractical.

New applications of SMALPs are rapidly emerging making membrane protein study more accessible and widespread. This meeting will explore the latest developments within the field, including novel polymers, techniques and targets, bringing together a wide range of researchers to share their findings.