The SARS-CoV-2 coronavirus encodes an essential papain-like protease domain as part of its non-structural protein (nsp)-3, namely SARS2 PLpro, that cleaves the viral polyprotein, but also removes ubiquitin-like ISG15 protein modifications as well as, with lower activity, Lys48-linked polyubiquitin. Structures of PLpro bound to ubiquitin and ISG15 reveal that the S1 ubiquitin-binding site is responsible for high ISG15 activity, while the S2 binding site provides Lys48 chain specificity and cleavage efficiency. To identify PLpro inhibitors in a repurposing approach, screening of 3,727 unique approved drugs and clinical compounds against SARS2 PLpro identified no compounds that inhibited PLpro consistently or that could be validated in counterscreens. More promisingly, noncovalent small molecule SARS PLpro inhibitors also target SARS2 PLpro, prevent self-processing of nsp3 in cells and display high potency and excellent antiviral activity in a SARS-CoV-2 infection model.

32 Coronaviruses, including SARS-CoV-2, encode multifunctional proteases that 33 are essential for viral replication and evasion of host innate immune 34 mechanisms. The papain-like protease PLpro cleaves the viral polyprotein, and 35 reverses inflammatory ubiquitin and anti-viral ubiquitin-like ISG15 protein 36 modifications 1,2 . Drugs that target SARS-CoV-2 PLpro (hereafter, SARS2 37PLpro) may hence be effective as treatments or prophylaxis for COVID-19, 38 reducing viral load and reinstating innate immune responses 3 . 39 We here characterise SARS2 PLpro in molecular and biochemical detail. 40 SARS2 PLpro cleaves Lys48-linked polyubiquitin and ISG15 modifications with 41 high activity. Structures of PLpro bound to ubiquitin and ISG15 reveal that the 42 S1 ubiquitin binding site is responsible for high ISG15 activity, while the S2 43 binding site provides Lys48 chain specificity and cleavage efficiency.44 We further exploit two strategies to target PLpro. A repurposing approach, 45 screening 3727 unique approved drugs and clinical compounds against 46 SARS2 PLpro, identified no compounds that inhibited PLpro consistently or 47 that could be validated in counterscreens. More promisingly, non-covalent 48 small molecule SARS PLpro inhibitors were able to inhibit SARS2 PLpro with 49 high potency and excellent antiviral activity in SARS-CoV-2 infection models. 50 51The COVID-19 pandemic unfolding globally in the first half of 2020 is caused by the 52 novel Coronavirus SARS-CoV-2, and has highlighted, amongst many things, the 53 general lack of antiviral small molecule drugs to fight a global coronavirus pandemic. 54Proteolytic enzymes are critical for viruses expressing their protein machinery as a 55 polyprotein that requires cleavage into functional units. As a result, viruses with 56 blocked protease activity do not replicate efficiently in cells; this concept extends to 57 coronaviruses 4 . Drugging the proteases in SARS-CoV-2 is therefore a current focus 58 of concerted global academic and pharma efforts 3 . 59 60 SARS-CoV-2 encodes two proteases, the papain-like protease (PLpro, encoded 61 within non-structural protein (nsp) 3), and 3-chymotrypsin-like 'main' protease 62 (3CLpro or Mpro, encoded within nsp5). PLpro generates nsp1, nsp2, and nsp3 63 (Figure 1a) and 3CLpro generates the remaining 13 non-structural proteins. After 64 3 their generation, the nsps assemble the viral replicase complex on host membranes, 65 initiating replication and transcription of the viral genome 1,5 . 66 67Viral proteases can have additional functions, and can for example act to inhibit host 68 innate immune responses that are mounted initially as an inflammatory response, 69 and subsequently as an interferon response. The interferon system generates an 70 antiviral state in host cells through transcriptional upregulation of more than 300 71 interferon-stimulated genes (ISGs), to efficiently detect and respond to viral threats 6 . 72Dysregulated inflammatory responses are a hallmark of COVID-19, and substantial 73 morb...

Highlights d USP28 forms an active dimer d USP25 adopts an auto-inhibited tetrameric state d Cancer-associated mutations lead to active USP25 d Neither substrate nor ubiquitin chains disrupt the USP25 tetramer

The pathogen Staphylococcus aureus causes a broad range of severe diseases and is feared for its ability to rapidly develop resistance to antibiotic substances. The increasing number of highly resistant S. aureus infections has accelerated the search for alternative treatment options to close the widening gap in anti-S. aureus therapy. This study analyses the humoral immune response to vaccination of Balb/c mice with sublethal doses of live S. aureus. The elicited antibody pattern in the sera of intravenously and intramuscularly vaccinated mice was determined using of a recently developed protein array. We observed a specific antibody response against a broad set of S. aureus antigens which was stronger following i.v. than i.m. vaccination. Intravenous but not intramuscular vaccination protected mice against an intramuscular challenge infection with a high bacterial dose. Vaccine protection was correlated with the strength of the anti-S. aureus antibody response. This study identified novel vaccine candidates by using protein microarrays as an effective tool and showed that successful vaccination against S. aureus relies on the optimal route of administration.

Based on the similarity between the active sites of the deubiquitylating and deneddylating enzyme ChlaDub1 (Cdu1) and the evolutionarily related protease adenain, a target-hopping screening approach on a focused set of adenain inhibitors was investigated. The cyanopyrimidine-based inhibitors identified represent the first active-site-directed small-molecule inhibitors of Cdu1. High-resolution crystal structures of Cdu1 in complex with two covalently bound cyanopyrimidines, as well as with its substrate ubiquitin, were obtained. These structural data were complemented by enzymatic assays and covalent docking studies to provide insight into the substrate recognition of Cdu1, active-site pocket flexibility and potential hotspots for ligand interaction. Combined, these data provide a strong basis for future structure-guided medicinal chemistry optimization of this cyanopyrimidine scaffold into more potent and selective Cdu1 inhibitors.

The COVID-19 pandemic continues unabated, emphasizing the need for additional antiviral treatment options to prevent hospitalization and death of patients infected with SARS-CoV-2. The papain-like protease (PLpro) domain is part of the SARS-CoV-2 non-structural protein (nsp)-3, and represents an essential protease and validated drug target for preventing viral replication. PLpro moonlights as a deubiquitinating (DUB) and deISGylating enzyme, enabling adaptation of a DUB high throughput (HTS) screen to identify PLpro inhibitors. Drug repurposing has been a major focus through the COVID-19 pandemic as it may provide a fast and efficient route for identifying clinic-ready, safe-in-human antivirals. We here report our effort to identify PLpro inhibitors by screening the ReFRAME library of 11,804 compounds, showing that none inhibit PLpro with any reasonable activity or specificity to justify further progression towards the clinic. We also report our latest efforts to improve piperidine-scaffold inhibitors, 5c and 3k, originally developed for SARS-CoV PLpro. We report molecular details of binding and selectivity, as well as in vitro absorption, distribution, metabolism and excretion (ADME) studies of this scaffold. A co-crystal structure of SARS-CoV-2 PLpro bound to inhibitor 3k guides medicinal chemistry efforts to improve binding and ADME characteristics. We arrive at compounds with improved and favorable solubility and stability characteristics that are tested for inhibiting viral replication. Whilst still requiring significant improvement, our optimized small molecule inhibitors of PLpro display decent antiviral activity in an in vitro SARS-CoV-2 infection model, justifying further optimization.

The phylum Apicomplexa contains several parasitic species of medical and agricultural importance. The ubiquitination machinery remains, for the most part, uncharacterised in apicomplexan parasites, despite the important roles that it plays in eukaryotic biology. Bioinformatic analysis of the ubiquitination machinery in apicomplexan parasites revealed an expanded ovarian tumour domain–containing (OTU) deubiquitinase (DUB) family inToxoplasma, potentially reflecting functional importance in apicomplexan parasites. This study presents comprehensive characterisation ofToxoplasmaOTU DUBs. AlphaFold-guided structural analysis not only confirmed functional orthologues found across eukaryotes, but also identified apicomplexan-specific enzymes, subsequently enabling discovery of a cryptic OTU DUB inPlasmodiumspecies. Comprehensive biochemical characterisation of 11ToxoplasmaOTU DUBs revealed activity against ubiquitin- and NEDD8-based substrates and revealed ubiquitin linkage preferences for Lys6-, Lys11-, Lys48-, and Lys63-linked chain types. We show that accessory domains inToxoplasmaOTU DUBs impose linkage preferences, and in case of apicomplexan-specific TgOTU9, we discover a cryptic ubiquitin-binding domain that is essential for TgOTU9 activity. Using the auxin-inducible degron (AID) to generate knockdown parasite lines, TgOTUD6B was found to be important forToxoplasmagrowth.

The Front Cover shows a covalent inhibitor (orange) simultaneously addressing the active sites of the Chlamydia trachomatis deubiquitylase 1 (Cdu1, green) and the adenovirus protease (adenain, red). The covalent bond is highlighted in yellow. The structural similarities of evolutionarily related proteases have been successfully harnessed for the repurposing of adenain inhibitors on Cdu1, demonstrating the potential of target‐hopping for the development of deubiquitylase (DUB) inhibitors. More information can be found in the Full Paper by Caroline Kisker, Christoph Sotriffer et al. on page 2014 in Issue 19, 2018 (DOI: 10.1002/cmdc.201800364).