The DDCB expertise includes drug discovery, chemical biology, assay development, high throughput screening (HTS), high content screening (HCS), virtual screening (VS), molecular modeling, chemoinformatics and ADMET studies.
The DDCB network provides following services:
Project and assay guidance and development support – all sites
- Joint advisory panel to help scientists with drug discovery technologies, processes and strategies
- Assay development and optimization is often a bottleneck in drug discovery and chemical biology so we provide this support, both in terms of hands-on support as well as guidance and access to the best possible instrumentation and technologies
Chemical screening – FIMM and Faculty of Pharmacy, UH, BioCity Turku
- World-class medium to high throughput screening and targeted HTS/HCS support
- Access to high throughput screening (HTS) automation and related instruments
- Emerging technologies and approaches include high content screening, label-free detection, ultra-miniaturized assay formats to allow screening with rare reagents and specimens as well as qPCR and lysate microarray readouts
- Development of novel technologies and miniaturized assay formats to reduce costs for end-users
Drug sensitivity and resistance screening (DSRT) and drug repurposing – FIMM, UH
- The DSRT platform at FIMM allows users to profile cellular model systems and ex vivo clinical samples against an annotated set of signal transduction inhibitors and approved oncology drugs
- The current platform offers a set of more than 500 clinical compounds (with translational implications)
- Analysis and interpretation support is provided by the DDCB network
- The DSRT platform is poised to provide opportunities for exciting translational outcomes, such as unexpected therapeutic benefits to diseases, as seen in our studies of leukemia samples
Imaging-based high throughput screening – FIMM, UH, BioCity Turku
Chemoinformatics, molecular modeling, and virtual screening – Biocenter Kuopio, Faculty of Pharmacy, UH, and BioCity Turku
- The DDCB network brings together nationwide expertise in virtual screening using different technologies and different target class experience
- DDCB network offers cherry-picking of hit compounds by chemoinformatics from the national chemical collection and confirmatory testing at screening sites, making follow-up testing affordable to the user
- Chemoinformatics for hit compound evaluation and optimization is also supported
Synthesis of novel drug candidates and hit/lead optimisation – Biocenter Kuopio
- Synthesis and optimization of novel target-based active compounds in close collaboration with molecular modelling and drug design laboratory
- Synthesis of novel transporter-utilizing tissue-, cell-, or organelle-targeted compounds/prodrugs to optimize ADMET properties of drug candidates
- Complimentary evaluation of drug delivery to the target sites (in vitro / in vivo)
Follow-up screening and testing – all sites
- Hit analoging, structure activity relationships, secondary screens, compound QC, prediction of in vivo properties for proof-of-concept
- Assay expertise at the participating partner sites all bring capacity to support users in follow-up testing beyond screening to take screening hits towards a proof-of-principle compound
- In particular, Faculty of Pharmacy offers world-class expertise in in vitro and in silico pharmacological profiling of compounds
- Faculty of Pharmacy also provides the capacity and expertise to validate integrity, stability and metabolism of chemicals with mass spectrometry
Access to large national chemical collections – FIMM, UH, BioCity Turku
- Compound libraries comprising more than 300 000 compounds
- Automated nanoscale dispensing systems allows for the users to access the compounds as part of pre-defined or in user-defined sets
- A collection of drugs and state-of-the-art bioactive tool compounds are also available one-at-a-time or in small subsets for biologists interested an affordable source for best-in-class inhibitors and other bioactives