Fabian Hink

ORCID: 0000-0003-3483-2596
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About
Contact & Profiles
Research Areas
  • Chemical Synthesis and Analysis
  • RNA and protein synthesis mechanisms
  • Computational Drug Discovery Methods
  • S100 Proteins and Annexins
  • Cell Image Analysis Techniques
  • Click Chemistry and Applications
  • Monoclonal and Polyclonal Antibodies Research
  • Viral Infectious Diseases and Gene Expression in Insects
  • Protein purification and stability
  • Pancreatic function and diabetes

University of Copenhagen
2022-2024

Abstract Many peptide hormones form an alpha-helix upon binding their receptors 1–4 , and sensitive detection methods for them could contribute to better clinical management. De novo protein design can now generate binders with high affinity specificity structured proteins 5,6 . However, the of interactions between short helical peptides is unmet challenge. Here, we describe parametric generation deep learning-based designing address this We show that RF diffusion generative model, picomolar...

10.1101/2022.12.10.519862 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-12-10

Interactions between proteins and α-helical peptides have been the focus of drug discovery campaigns. However, large interfaces formed multiple turns an α-helix a binding protein represent significant challenge to inhibitor discovery. Modified featuring helix-stabilizing macrocycles shown promise as inhibitors these interactions. Here, we tested ability N-terminal side-chain thioether-cyclized inhibit Mcl-1, by screening trillion-scale library. The enriched were lariats small,...

10.1021/jacs.4c05378 article EN other-oa Journal of the American Chemical Society 2024-08-25

Interactions between proteins and α-helical peptides are abundant in the human cell. Many of these interactions linked to disease have been focus drug discovery campaigns. However, large interfaces formed multiple turns α-helix a binding protein represent significant challenge inhibitor discovery. Modified featuring helix-stabilizing macrocycles shown promise as inhibitors interactions. Here, we tested ability N-terminal side-chain thioether-cyclized inhibit Mcl-1, by screening...

10.26434/chemrxiv-2024-nkfv0 preprint EN cc-by-nc-nd 2024-04-02
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