Augustinas Silale

Augustinas Silale

@augustsilale.bsky.social

Structural biology, membrane proteins, microbiology. Postdoc. Newcastle upon Tyne. 🧪🧫❄️🔬🇱🇹🏳️‍🌈

197 followers138 following13 posts

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Our study on Bacteroides iron piracy is now out in @pnas.org. We show how surface-exposed lipoproteins bind xenosiderophores with different iron-chelating chemistries and propose a mechanism for xenosiderophore import across the outer membrane. Lots of structures (mostly X-ray this time)!

doi.orgStructural basis of iron piracy by human gut Bacteroides | PNASIron is an essential element that can be growth-limiting in microbial communities, particularly those present within host organisms. To acquire iro...

Augustinas Silale reposted

Are you a motivated researcher interested in bacteria-host interactions? We have postdoc position available in my lab to join our Wellcome Trust funded collaborative team. We will study the role and regulation of the enigmatic sphingolipids in E. coli. Please share. www.jobs.ac.uk/job/DSX115/r...

jobs.ac.ukResearch Assistant/ Associate in Bacteria-Host Interactions at Newcastle UniversityExplore an exciting academic career as a Research Assistant/ Associate in Bacteria-Host Interactions. Don't miss out on other academic jobs. Click to apply and explore more opportunities.

Augustinas Silale reposted

Really pleased to share our latest preprint, the result of a fantastic Anglo-Scots collaboration www.biorxiv.org/content/10.6... We uncover how the bacterial Rhesus protein NeRh50 diverges from canonical ammonium transporters 👇🧵 #CryoEM #MembraneProteins #MassSpectrometry #AmmoniumTransport

Augustinas Silale reposted

Augustinas Silale reposted

Replying to @lislowe.bsky.social

Also #glycotime of course! The enzymes are GH172 arabinofuranosidases that break down mycobacterial cell wall glycans. They multimerise into dimers/trimers/hexamers/dodecamers and they are (I admit I’m biased) beautiful enzymes!

Augustinas Silale reposted

Happy to share our recent story on the Type VII secretion system. Here were present new insights into the regulation of secretion mediated by the central pore. Thanks to all authors involved in the work. 🙂

bioRxiv Microbiology@biorxiv-microbiol.bsky.social

Intrinsic flexibility of Type VII secretion central pore is required for substrate translocation https://www.biorxiv.org/content/10.64898/2026.07.31.742005v1

Augustinas Silale reposted

Augustinas Silale reposted

This has been such a fun collaboration and a great example of team science

Patrick Moynihan@pmoyniha.bsky.social

New paper in collaboration with @proftracypalmer.bsky.social, @lislowe.bsky.social and many more. We show that mycobacteria produce Type VII secreted anti-bacterial protein toxins. Excited to explore this new area of mycobacterial biology. www.nature.com/articles/s41...

Augustinas Silale reposted

Out after a lot of hard work from many people. When we first found arabinanase enzymes in mycobacteria we started looking into their roles in cell remodelling & pathogenesis. Did not expect to find that some species had weaponised them to kill competitors! Myco are endlessly surprising. #glycotime

Patrick Moynihan@pmoyniha.bsky.social

New paper in collaboration with @proftracypalmer.bsky.social, @lislowe.bsky.social and many more. We show that mycobacteria produce Type VII secreted anti-bacterial protein toxins. Excited to explore this new area of mycobacterial biology. www.nature.com/articles/s41...

Augustinas Silale reposted

Check out our latest T7SS toxin story. These reverse toxins aren’t as rare as we thought!

bioRxiv Microbiology@biorxiv-microbiol.bsky.social

A novel reverse lipase toxin substrate of the Staphylococcus aureus type VII secretion system https://www.biorxiv.org/content/10.64898/2026.06.22.733114v1

Augustinas Silale reposted

Augustinas Silale reposted

Augustinas Silale reposted

Augustinas Silale reposted

Augustinas Silale reposted

Augustinas Silale reposted

65 years after Peter Mitchell’s chemiosmotic theory, we report an association between ATP synthase and the electron transport chain. In the preprint led by @longzhou88.bsky.social, we describe a large supercomplex and show how the supramolecular organization contribute to oxidative phosphorylation 🧵

langtaosha.org.cnA Supercomplex Incorporating Both Electron Transport Chain and ATP SynthaseThe mitochondrial oxidative phosphorylation system powering most aerobic organisms is typically depicted as two spatially segregated machineries(1): electron transport chain complexes I-IV (ETC CI-CIV

Augustinas Silale reposted

Unbelievably proud of the work that everyone has put into this paper. Really grateful for such fab colleagues! Mycobacteria continue to be (subjectively) the most interesting bacteria 🤭

Patrick Moynihan@pmoyniha.bsky.social

We've been we've been working on this for quite a while now (hopefully published soon). Grateful to @proftracypalmer.bsky.social for concinving me & @lislowe.bsky.social that mycobacteria produce inter-bacterial toxins. Team science, led by @sambenedict5.bsky.social www.biorxiv.org/content/10.6...

Augustinas Silale reposted

Replying to @lislowe.bsky.social

A GH with an immunity protein that binds with nM affinity and looks like this 🤩. Bacteria are always surprising us

Augustinas Silale reposted

We’ve been sciencing! M abscessus makes a arabinanase toxin to chop up the cell wall of competitor mycobacteria! #glycotime 🦠 thanks to @wellcometrust.bsky.social for the funding that makes this collaborative work possible! Also Sam’s structures are 😍 and Jean-Lou did some lovely biochem

Patrick Moynihan@pmoyniha.bsky.social

We've been we've been working on this for quite a while now (hopefully published soon). Grateful to @proftracypalmer.bsky.social for concinving me & @lislowe.bsky.social that mycobacteria produce inter-bacterial toxins. Team science, led by @sambenedict5.bsky.social www.biorxiv.org/content/10.6...

Augustinas Silale reposted

Augustinas Silale reposted

Great to see Arnaud Basle, facility manager of our structural biology facility @nusbf.bsky.social there representing @newcastleuni.bsky.social 👏

Instruct-ERIC@instruct-eric.bsky.social

The Instruct Best Practices in Cryo-EM Workshop is an opportunity for facility staff and technicians to exchange experiences and the latest developments EM - thank you to all participants for a great meeting so far in Milan! @thermofishersci.bsky.social #IMAGINE @humantechnopole.bsky.social

Augustinas Silale reposted

I’ve officially started my lab at Monash University! 🎉 We’re diving into #cellgrowth and #lysosome biology, through the lens of molecular #structure and mechanism. I’m thrilled to say that PhD student scholarships are available—so please share widely and get in touch if you’re interested. 🤩

Augustinas Silale reposted

Augustinas Silale reposted

Still lots of time to apply for this exciting project with us. Please share and encourage interested students to get in touch.

James Connolly@ruamicro.bsky.social

PhD position available in our team to study how UPEC exploits metals to successfully colonise the host gut. Cool collaboration with @thecopperdoctor.bsky.social and @banzhaflab.bsky.social Please share and get in touch for more details

Augustinas Silale reposted

Augustinas Silale reposted

💊 We are excited to share our preprint that describes an inhibitor of the widespread and highly conserved Two-Partner Secretion (TPS) system that is critical for Gram-negative pathogens to export a multitude of diverse virulence factors. (1/6) www.biorxiv.org/content/10.6...

biorxiv.orgFirst inhibitor of a bacterial two-partner secretion system.Two-partner secretion system transporter proteins (TpsB) are widely conserved across Gram-negative pathogens. TpsB family proteins secrete exoprotein virulence factors that perform a myriad of functions such as adhesion and immune modulation. Despite their incredible importance in bacterial infectious disease, TpsB inhibitors have not yet been discovered. Here, we describe a potent inhibitor of FhaC, a TpsB protein produced by Bordetella spp . FhaC secretes the exoprotein FhaB that is essential for the establishment of whooping cough. We designed a peptide called P1 that we predicted would prevent substrate binding and lock FhaC in a secretion-inactive state. Simulations and biochemical assays supported our hypothesis and identified interactions important for P1 binding to FhaC. Strikingly, we observed that the peptide strongly inhibited FhaB secretion from clinical isolates and broadly reduced correlates of virulence. Together, this work provides a strong case for further development of a novel class of anti-TpsB anti-virulence compounds. ### Competing Interest Statement The authors have declared no competing interest. National Institute of Allergy and Infectious Diseases, R21AI180112

Augustinas Silale reposted

Augustinas Silale reposted