Kinaxo Biotechnologies has announced that it has entered into a two-year collaboration with Boehringer Ingelheim.
Under the agreement, Kinaxo will apply its platform technologies to studies on drug mode of action and target identification.
Building on its existing quantitative Cellular Target profiling capabilities, Kinaxo will employ high-end mass spectrometry technologies to quantitatively analyse post-translational modifications of proteins.
This new service will make it possible to determine the effects of compounds on proteome-wide signal transduction pathways, providing a detailed picture of their in-vivo mode of action in cultured cells or animal tissue.
Such analyses will also facilitate identifying new biomarkers and drug targets.
In the initial phase of this collaboration, Kinaxo will undertake two studies on behalf of Boehringer Ingelheim.
The first will be a cell line analysis project to measure the effects of an enzyme inhibitor on the acetylation status of the cellular proteome.
In the second study, Kinaxo will use its phosphoproteomics platform to determine differences in the signal transduction pathway activation status of a specific neuronal tissue when comparing wild type with a genetically-modified mouse strain modelling a defined disease state.
The aim of this study is to identify new drug targets.
Kinaxo's addition of post-translational modification profiling to the current Cellular Target profiling service helps generate a comprehensive picture of a compound's mode of action.
Most protein kinases are positively or negatively regulated through phosphorylation by other kinases.
Therefore, differential analysis of the complete cellular 'phosphoproteome' upon kinase inhibitor treatment provides a highly informative and direct insight into the compound's mode of action.
Kinaxo's new services combine a mass spectrometry platform with Stable Isotope Labelling by Amino acids in Cell culture (SILAC) technology, as developed in the laboratory of professor Matthias Mann at the Max-Planck Institute of Biochemistry, Martinsried, Germany.
With the creation of a 'SILAC mouse' Matthias Mann and colleagues recently extended the technology to analysing tissue samples from animal models.
'The SILAC platform is a powerful tool that enables one to quantitatively compare post-translational modifications across multiple biological samples.
'Initially applied to cell lines we have developed the "SILAC mouse", which significantly extends the capability, since we can now also analyse and compare any mouse tissue,' said professor Mann.
Dr Andreas Jenne, Kinaxo's chief executive officer, added: 'Among other applications, our customers will now be able to determine the quantitative effect of their compounds on cellular signalling pathways, as well as identify and quantify compound target interactions, all in a proteome-wide fashion.
'This will provide critical cell-based and in-vivo information on a compound's mechanism of action to support drug programme decision making.'
