Die AG Cabrele

We are interested in the inhibitors of DNA binding and cell differentiation Id1-4 belonging to the family of the helix-loop-helix (HLH) transcription factors. They are important during development, cell fate and lineage determination, neurogenesis and angiogenesis. Also, upregulated Id-protein expression has been observed in several cancer types and has been associated to tumor angiogenesis, migration and invasion. Therefore, the Id proteins can be considered interesting therapeutic targets.

Further, we collaborate with colleagues from the  University of Regensburg (Germany) to develop analogs of the natural peptide hormones NPY and hPP with selective agonistic/antagonistic binding to their G-protein coupled receptors (the NPY Yn-receptors). 

Selected publications:
The Recombinant Inhibitor of DNA Binding Id2 Forms Multimeric Structures via the Helix-Loop-Helix Domain and the Nuclear Export Signal, C. Roschger, M. Schubert, C. Regl, A. Andosch, A. Marquez, T. Berger, C.G. Huber, U. Lütz-Meindl, C. Cabrele (2018) Int. J. Mol. Sci. 19(4). pii: E1105. doi: 10.3390/ijms19041105
Synthesis and Conformational Properties of Protein Fragments Based on the Id Family of DNA-Binding and Cell-Differentiation Inhibitors, S. Kiewitz, C. Cabrele (2005) Biopolymers (Peptide Sci.) 80, 762-774.
Synthesis and Conformational Analysis of Id2 Protein Fragments: Impact of Chain Length and Point Mutations on the Structural HLH Motif, N. Colombo, C. Cabrele (2006) J. Peptide Sci. 12, 550-558.
Stepwise Solid-Phase-Synthesis and Spontaneous Homodimerization of the Helix-Loop-Helix Protein Id3, J. Svobodová, C. Cabrele (2006) ChemBioChem 7, 1164-1168.
Synthesis and Conformation of an Analog of the Helix-Loop-Helix Domain of the Id1 Protein Containing the O-Acyl Iso-Prolyl-Seryl Switch Motif, M. Beißwenger, T. Yoshiya, Y. Kiso, C. Cabrele, (2010) J. Peptide Sci. 16, 303-308.
Wenn Proteine ihren Partner wechseln (When proteins chainge their partner), C. Cabrele (2011) BIOSpektrum (Spektrum Akademischer Verlag) 1, 12.
G protein-coupled receptors function as logic gates for nanoparticle binding and cell uptake, W. Hild, K. Pollinger, A. Caporale, C. Cabrele, M. Keller, N. Pluym, A. Buschauer, R. Rachel, J. Tessmar, M. Breunig, A. Goepferich, (2010) Proc. Natl. Acad. Sci. USA 107, 10667-10672.

We use the chemical approach to prepare polypeptides reproducing the native or modified sequences of the Id proteins (119 up to 165 residues) and other biological targets. Most of our syntheses are carried out on the solid phase by applying Fmoc-chemistry.

Selected publications:
Synthesis and Conformational Analysis of Id2 Protein Fragments: Impact of Chain Length and Point Mutations on the Structural HLH Motif, N. Colombo, C. Cabrele (2006) J. Peptide Sci. 12, 550-558.
Stepwise Solid-Phase-Synthesis and Spontaneous Homodimerization of the Helix-Loop-Helix Protein Id3, J. Svobodová, C. Cabrele (2006) ChemBioChem 7, 1164-1168.

Bioactive peptides are powerful scaffolds for the development of new therapeutic agents. However, it is essential to overcome some drawbacks associated to their low metabolic stability and bioavailability. We are interested in the development of chemically modified bioactive peptides, in order to provide them of proteolytic stability and target specificity. Suitable chemical tools are, among others, unnatural, conformationally restricted amino acids, and macrocyclizations.

Selected publications:
Side-Chain Cyclization Based on Serine Residues: Synthesis, Structure and Activity of a Novel Cyclic Analogue of the Parathyroid Hormone Fragment 1-11, A. Caporale, M. Sturlese, L. Gesiot, F. Zanta, A. Wittelsberger, C. Cabrele, (2010) J. Med. Chem. 53, 8072-8079.

Many proteins exert their action by interacting with specific protein targets and forming active complexes that initiate a signal cascade. Also the Id proteins negatively modulate DNA transcription by sequestering basic-HLH transcription factors in heterodimers that are devoid of the ability to bind the DNA. The Id-HLH domain is essential for protein-protein interaction, thus representing an interesting target for molecular recognition by means of artificial agents to modulate the Id-protein activity. We use two different approaches to target the Id-HLH dimerization domain: (a) identification of peptide-based ligands and (b) application of artificial receptors for amino-acid side-chain recognition (collaboration with  Prof. B. König at the University of Regensburg).
The conformation of a protein depends not only on its primary structure, but also on extrinsic factors such as temperature, ionic strength, pH and hydrophobicity of the solvent. Due to their biological relevance and to their application in different fields spreading from drug formulation to bionanotechnology, it is worthwhile to investigate the behavior of proteins upon environmental changes. Based on the use of peptide models, we are interested in the elucidation of the interplay between different secondary structure motifs and surrounding molecules from the solvent and other additives (collaboration within the Excellence Cluster RESOLV of the Ruhr-University Bochum). 
Selected publications:
Recognition of the Helix-Loop-Helix Domain of the ld Proteins by an Artificial Luminescent Metal Complex Receptor, S. D. Kiewitz, M. Kruppa, A. Riechers, B. König, C. Cabrele (2008) J. Mol. Recognit. 21, 79-88.
Synthetic Peptides Containing a Conserved Sequence Motif of the Id Protein Family Modulate Vascular Smooth Muscle Cell Phenotype, S. Pellegrino, N. Ferri, N. Colombo, E. Cremona, A. Corsini, R. Fanelli, M. L. Gelmi, C. Cabrele (2009) Bioorg. Med. Chem. Lett. 19, 6298-6302.
How Ionic Liquids Can Help to Stabilize Native Proteins, H. Weingärtner, C. Cabrele, C. Herrmann (2011) Phys. Chem. Chem. Phys. 14, 415-426.

  
Selected publications:
Biomimetic Soluble Collagen Purified from Bones, A. M. Ferreira, P. Gentile, S. Sartori, C. Pagliano, C. Cabrele, V. Chiono, G. Ciardelli (2012) Biotechnol. J. doi: 10.1002/biot.201200184.