Redox Regulation in Health and Disease Coordinated and Hosted by Prof

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Autumn 2020 ISMB Seminar Series Redox regulation in health and disease Coordinated and hosted by Prof. Ivan Gout and Dr. Amandine Marechal, except where noted. Talks take place on Wednesdays from 1-2pm on Microsoft Teams via the link in promotional emails. Towards Understanding Cellular Redox Regulation 30th September Prof. Helmut Sies, Institute for Biochemistry and Molecular Biology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany Redox regulation in ageing 7th October Dr. Helena Cochemé, Redox Biology Group, Imperial College, London, UK A new twist on type IV pili - cryoEM reveals two distinct filaments assembled by the same bacterium 14th October Dr. Vicki Gold, University of Exeter, Exeter, UK Special host: Prof. Helen Saibil Glutathione: an antioxidant or a signalling molecule? 21st October Prof. Pietro Ghezzi, Brighton and Sussex Medical School, Brighton, UK Cryo-EM: From Blobology to Drug Design 28th October Dr. Basil Greber, Institute of Cancer Research, London, UK Special host: Dr. Jerome Gouge Redox regulation of selective autophagy 4th November Dr. Viktor Korolchuk, Newcastle University, Newcastle upon Tyne, UK Targeting redox-regulated metabolons in Alzheimer's disease 11th November Prof. Myra Conway, University of the West of England, Bristol, UK The role of redox-regulated PKG in pulmonary hypertension 18th November Dr. Olena Rudyk, School of Cardiovascular Medicine & Sciences, Kings College, London, UK Persulfidation in control of cell function 25th November Prof. Elias Arnér, Karolinska Institutet, Sweden Redox signaling in vascular endothelial cells under defined ambient oxygen levels 2nd December Prof. Giovanni Mann, Free Radical Biology & Medicine, Kings College, London, UK The Type VII protein secretion system of Staphylococcus aureus 9th December Prof. Tracy Palmer, Newcastle University, Newcastle upon Tyne, UK Special host: Prof. Helen Saibil www.ismb.lon.ac.uk/seminar.html .

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Microbial Musings – December 2020
EDITORIAL Thomas, Microbiology 2020;166:1107–1109 DOI 10.1099/mic.0.001019 OPEN ACCESS Microbial Musings – December 2020 Gavin H. Thomas* As we end this extraordinary year, the importance of micro- resistance (AMR)’ to our ‘Antimicrobials and AMR’ theme. biology continues to be demonstrated in our daily lives in Next month I will be announcing a significant number of new ways that we would never have predicted 12 months ago. This editors to handle submissions within our revised topic areas. month in the UK, the identification of a new variant of severe The first paper from this issue to highlight is one that would acute respiratory syndrome coronavirus 2 (SARS- CoV-2) fit nicely into the new Plant microbiology and soil health through the continuing work of the COVID-19 Genomics topic, as it is around the biology of two Bacillus species strains Consortium (@CovidGenomicsUK) led to an almost imme- that are currently used as biocontrol agents in China, and diate change in government policy, and while the manifesta- more specifically are used to protect oil seed rape crop from tions of the new variant are being uncovered, it is an example a pathogenic fungal infections. The work from Alex Mullins of evolution occurring in real time in front of the eyes of the (@AlexJMullins), collaborating with Eshwar Mahenthiral- general public. The development and delivery of multiple new ingam and Gordon Webster at the University of Cardiff, UK, vaccines against the virus are a true illustration that biology and colleagues at the Oil Crops Research Institute of Chinese has the potential to be the greatest technology of the 21st Academy of Agricultural Sciences, Wuhan, PR China, aimed century.
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Dr. Annika Guse [email protected]
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The Tata Component of the Twin-Arginine Protein Transport System Forms Channel Complexes of Variable Diameter
The TatA component of the twin-arginine protein transport system forms channel complexes of variable diameter Ulrich Gohlke*†, Lee Pullan*‡, Christopher A. McDevitt§, Ida Porcelli§, Erik de Leeuw§, Tracy Palmer¶ʈ, Helen R. Saibil*, and Ben C. Berks§ *Institute of Structural Molecular Biology, School of Crystallography, Birkbeck College, Malet Street, London WC1E 7HX, United Kingdom; §Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, United Kingdom; ¶School of Biological Sciences, University of East Anglia, Norwich NR4 7TJ, United Kingdom; and ʈDepartment of Molecular Microbiology, John Innes Centre, Norwich NR4 7UH, United Kingdom Edited by William T. Wickner, Dartmouth Medical School, Hanover, NH, and approved June 8, 2005 (received for review April 29, 2005) The Tat system mediates Sec-independent transport of folded diameter (15, 17). TatBC has been shown to act as the receptor precursor proteins across the bacterial plasma membrane or the element of the translocation pathway (13, 16, 18), and TatC has chloroplast thylakoid membrane. Tat transport involves distinct been shown to contain the primary binding site for the signal high-molecular-weight TatA and TatBC complexes. Here we report peptide (18). The function of TatA is less clear. It is known that the 3D architecture of the TatA complex from Escherichia coli TatA is required subsequent to substrate recognition by the obtained by single-particle electron microscopy and random con- TatBC complex (16, 18, 19), and this has led to the suggestion ical tilt reconstruction. TatA forms ring-shaped structures of vari- that TatA constitutes the protein-conducting channel of the Tat able diameter in which the internal channels are large enough to system.
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Complete Dissertation
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Declarations of Interest
DECLARATIONS OF INTEREST Please refer to the attached guidance notes before completing this register entry. In addition to guidance on each section, examples of information required are also provided. Where you have no relevant interests in the relevant category, please enter ‘none’ in the register entry. Please return this form by e-mail and also a printed signed copy in addition to the e-mailed version; updates after this need only be provided electronically. Name: Professor Tracy Palmer Please list all MRC bodies you are a member of: E.g. Council, Strategy Board, Research Board, Expert Panel etc and your position (e.g. chair, member). • Infection and Immunity Board Main form of employment: Name of University and Department or other employing body (include location), and your position. Professor of Molecular Microbiology College of Life Sciences University of Dundee Dundee DD1 5EH Research group/department web page: Provide a link to any relevant web pages for your research group or individual page on your organisation’s web site. • http://www.lifesci.dundee.ac.uk/people/tracy-palmer Please give details of any potential conflicts of interests arising out of the following: 1. Personal Remuneration: Including employment, pensions, consultancies, directorships, honoraria. See section 1 for further guidance. Employed by the University of Dundee, funded by the Scottish Higher Education Funding Council. Please note that I am also partly funded by a Royal Society Wolfson Merit Award from 2011 - 2016 I am an editor for the journal Molecular Microbiology. This pays an honorarium. External examiner at Imperial College for the Wellcome Trust funded Mres ‘Molecular & Cellular Basis of Infection’ - honorarium 2.
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A Complete Bibliography of Publications in the Journal of Cell Biology: 2010–2014
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