The pharmacological relevance of pro-peptide of GDNF family members

Lead Research Organisation: University of Cambridge
Department Name: Biochemistry

Abstract

Theme: Bioscience for Health

Type 2 Diabetes and metabolic diseases more generally together with cardiovascular diseases affect increasing numbers of people. There is interest in regenerative approaches for both pancreaticbeta-cells and cardiomyocytes. TGFbfamily proteins play an important part in cell development and differentiation as well as in disease and BMP2 has been successfully developed and is marketed as a regenerative factor for bone growth. GDNF subfamily of growth factors are normally used as neurotrophic factors, but neurturin in particular has been shown to have beneficial effect on diabetic animals, lowering their glucose levels in insulin dependent manner. While the mechanism for this is unknown, the use of neurturin as therapeutic agent is compromised by its poor pharmacodynamic properties and limited tissue distribution. As neurturin, like all GDNF-like proteins, is synthesised as larger precursors. We have recently shown how activin A has very different properties when complexed with its pro-peptide. We hypothesise that the precursor forms of neurturin are similarly different from the mature protein so far used in the assessment of therapeutic potential. The aim of this project is to produce pre-cursor forms of neurturin and analyse its biochemical, biological and structural activities. At the same time we will analyse the effect of the pro-peptide on the bioavailability and tissue distribution of the growth factor, with an aim of developing more effective therapeutic agents.

Publications

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Studentship Projects

Project Reference Relationship Related To Start End Student Name
BB/M011194/1 01/10/2015 31/03/2024
1800648 Studentship BB/M011194/1 01/10/2016 31/03/2021 Matthew Ratcliff
 
Description The aim of this project was to produce pre-cursor forms of neurturin and analyse its biochemical, biological and structural activities. Pre-cursor forms of neurturin have now been produced and biological activity has been assessed using cell based assays. This work has been replicated for another pharmaceutically relevant protein. A model for the shape and structure of the pre-cursor form of neurturin has been generated and information on domain interactions has been obtained.
Exploitation Route Infomation on the properties of both growth factor proteins studied here could inform future directions at Medimmune/AstraZeneca (our collaboators) and others that would be interested in these proteins as therapeutics.
Sectors Pharmaceuticals and Medical Biotechnology

 
Description Medimmmune (AstraZeneca) 
Organisation AstraZeneca
Department MedImmune
Country United Kingdom 
Sector Private 
PI Contribution Samples for this project were produced at the University of Cambridge by award holder (Matthew Ratcliff) using expertise in protein production. Results/data were shared with collaborators.
Collaborator Contribution Medimmune facilities were then used to analyse samples by award holder (Matthew Ratcliff). Training and expertise in the use of the facilities to perform the assays developed at Medimmune were provided.
Impact Collaboration is not multi-disciplinary. Activity of different protein samples produced has been assessed through this collaboration.
Start Year 2016