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Main acceptance window for Samsung Peptide's PolyPeptide tender ends today

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Photo: Ryan McGuire / StockSnap (CC0) / own upload

Samsung Biologics, through its Swiss subsidiary Samsung Peptide AG, set the main offer period for its public tender for all publicly held shares of PolyPeptide Group AG to run from 15 September to 12 October 2026 at 4 p.m. Swiss time. The offer price is CHF 44.31 net cash per share (about CHF 1.46 billion equity value), with a minimum acceptance threshold of 66â…”% on a fully diluted basis, regulatory approvals and other customary conditions. PolyPeptide's board recommended acceptance; the largest individual shareholder undertook to tender its stake. Settlement, if conditions are met, is expected by the end of 2026.

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Automated OSAR platform assembles large NRPS clusters without custom DNA synthesis

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Photo: André Robillard / StockSnap (CC0) / own upload

Researchers at the Shenzhen Institute of Synthetic Biology, Jinan University and UC Berkeley reported in Nature Communications on 11 October OSAR, an automated one-step assembly and refactoring workflow that uses algorithmic primer design and yeast homologous recombination to clone large non-ribosomal peptide synthetase clusters without de novo DNA synthesis. Of 34 bacterial NRPS clusters (7–78 kb), 31 assembled successfully, and Bacillus subtilis expression yielded 29 peptides from 10 clusters, including products consistent with cryptic module skipping or premature release.

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Opsonic peptide OP18 helps macrophages clear radiation-linked extracellular traps in vitro

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Photo: Greg Rakozy / StockSnap (CC0) / own upload

Researchers at the Feinstein Institutes for Medical Research reported in Frontiers in Immunology on 12 October that the opsonic peptide OP18, which targets damage-associated molecular patterns including histone H3 and HMGB1, increased uptake of radiation-associated macrophage extracellular traps by cultured macrophages via αvβ3 integrin and endo-lysosomal trafficking. Clearance was linked to lower MET-driven mitochondrial stress, restored metabolic readouts and a trend toward higher IL-10. The study is cell-culture work.

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Gold–titania Janus particles enrich modified peptides and capture serum exosomes for MS

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Photo: Free Nature Stock / StockSnap (CC0) / own upload

Researchers at Jilin University and SCIEX reported in Analytical Chemistry on 9 October an Au–TiO₂ Janus material whose gold face enriches palmitoylated peptides via Au–S bonding while the titania face enriches phosphorylated peptides and captures serum exosomes. Coupled to mass spectrometry, the workflow showed strong selectivity for both peptide modification classes and, in a serum profiling experiment, flagged four dual-modified proteins that differed between non-small-cell lung cancer samples and controls. The paper is an analytical methods report.

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Modular synthesis builds antimicrobial peptidomimetics that disrupt bacterial membranes

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Photo: Tohm Brigitte / StockSnap (CC0) / own upload

Researchers at the University of Parma and the Helmholtz Centre for Infection Research reported in the Journal of Medicinal Chemistry on 8 October a library of antimicrobial peptidomimetics inspired by magainin-related and brilacidin-like designs. Side-chain length proved important for insertion into phospholipid bilayers. A modular route produced diverse analogues for structure–activity work; compounds were tested against clinically relevant pathogens in laboratory assays, with preliminary data pointing to a membranolytic mechanism. The study is synthetic and in vitro microbiology.

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De novo miniproteins designed to block bacterial adhesins behind urinary tract infections

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Photo: Wil Stewart / StockSnap (CC0) / own upload

A Nature Communications paper published online on 9 October describes de novo–designed miniprotein binders to the chaperone-usher pili adhesins FimH from uropathogenic Escherichia coli and Abp from Acinetobacter baumannii. The antagonists showed high specificity and stability, disrupted recognition of host receptors and blocked biofilm formation in laboratory assays, and were evaluated in murine models of uncomplicated and catheter-associated urinary tract infection. The work is preclinical protein design.

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