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Liepe, J.

Publications and source records attributed to Liepe, J..

3 recordsLinked to original sources

PMGen: From Peptide-MHC Prediction to Neoantigen Generation

Accurate structural modeling of peptide-MHC (pMHC) complexes is a prerequisite for understanding adaptive immunity and developing data-driven immunotherapies. However, current tools are often limited by narrow class coverage, restricted peptide lengths, or insufficient accuracy for downstream design tasks. Here, we introduce PMGen (Peptide MHC Generator), an integrated framework for structure prediction and structure-guided design of variable-length peptides across MHC class I and II. By introducing Initial Guess and Template Engineering as strategies to enforce anchor constraints in AlphaFold2, PMGen achieves state-of-the-art structural fidelity with median peptide core RMSDs of 0.54 [A] for MHC-I and 0.33 [A] for MHC-II, outperforming five state-of-the-art methods. We further demonstrate that PMGen captures the subtle structural impact of single-point neoantigen mutations and that model confidence (pLDDT) reliably correlates with structural accuracy. We investigated two potential applications of our framework: structure-aware peptide design and generating data for machine learning (ML) models. To this end, we introduced a framework to sample peptides with preserved structures and improved binding affinity. As an example for ML application, we fine-tuned ProteinMPNN on PMGen-modeled structures. This improved sequence recovery from 0.19 to 0.40 compared to the baseline. Ultimately, PMGen bridges the gap between high-fidelity structural prediction and downstream sequence design, offering a scalable solution to generate the large-scale, high-quality structural datasets required to train advanced predictive models in immunology. Available at https://github.com/soedinglab/PMGen.

bioinformatics↗

Chemical crosslinking extends and complements UV crosslinking in analysis of RNA/DNA nucleic acid-protein interaction sites by mass spectrometry

UV (ultra-violet) crosslinking with mass spectrometry (XL-MS) has been established for identifying RNA- and DNA-binding proteins along with their domains and amino acids involved. Here, we explore chemical XL-MS for RNA-protein, DNA-protein, and nucleotide-protein complexes in vitro and in vivo. We introduce a specialized nucleotide-protein-crosslink search engine, NuXL, for robust and fast identification of such crosslinks at amino acid resolution. Chemical XL-MS complements UV XL-MS by generating different crosslink species, increasing crosslinked protein yields in vivo almost four-fold, and thus it expands the structural information accessible via XL-MS. Our workflow facilitates integrative structural modelling of nucleic acid-protein complexes and adds spatial information to the described RNA-binding properties of enzymes, for which crosslinking sites are often observed close to their cofactor-binding domains. In vivo UV and chemical XL-MS data from E. coli cells analysed by NuXL establish a comprehensive nucleic acid-protein crosslink inventory with crosslink sites at amino acid level for more than 1500 proteins. Our new workflow combined with the dedicated NuXL search engine identified RNA crosslinks that cover most RNA-binding proteins, with DNA and RNA crosslinks detected in transcriptional repressors and activators.

biochemistry↗

Phosphoproteomics identifies targets of Mos-MAPK regulating translation and spindle organization in oocyte meiosis

The Mos kinase activates the ERK/MAPK pathway during oocyte meiosis, controlling essential meiotic functions in species across metazoa. However, despite its significance, the molecular targets of Mos-MAPK remain largely unidentified. Here, we addressed this question using starfish oocytes ideally suited to combine cellular assays with phosphoproteomics. This revealed CPE-mediated mRNA polyadenylation as a prominent target of Mos-MAPK, and we show that translation is required to drive the second meiotic division. Secondly, we identify a well-defined subset of cytoskeletal regulators as targets of Mos-MAPK. We show that this regulation is critical to ensure the asymmetry of meiotic divisions primarily by reducing the growth of astral microtubules. This allows positioning of the spindle directly beneath the cortex and prevents the separation of spindle poles in anaphase, thereby minimizing polar body size. Thus, by phosphoproteomics we reveal molecular modules controlled by Mos-MAPK explaining how this single, conserved kinase can act as a switch between the mitotic and meiotic division programs.

cell biology↗