Dr Roz Jenkins BSc (Hons), PhD
Research Fellow and Lab Manager, CDSS/ITM Proteomics Facility Pharmacology & Therapeutics
- About
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Research
Mass spectrometry applied to drug safety
The CDSS/ITM mass spectrometry facility is equipped with advanced instrumentation, facilitating an integrated, parallel approach to the study of biology and chemistry. Four instruments are dedicated to the analysis of small molecules, with targeted analyses allowing for sensitive and specific absolute quantification of drugs and their metabolites, and of endogenous analytes. One of these instruments is GCLP certified.
A further four instruments are dedicated to the analysis of proteins and peptides, with the capability for both discovery and targeted proteomics pipelines. We have expertise in label-dependent (iTRAQ, ICAT, SILAC) and label-free (SWATH, DIA) quantitative approaches that allow a global view of protein expression in, for instance, health and disease or following drug therapy. We also have instruments that are capable of quantifying peptides of interest at low attomole (femtogram) levels of sensitivity using targeted multiple reaction monitoring. These are particularly useful when good quality antibodies are not available.
A particular expertise of the facility is the characterisation of unconventional protein modifications. These may be as a result of direct drug or metabolite binding, but may also be a result of perturbed physiological processes leading to unexpected biochemical modification of protein. The integration of biology, chemistry and mass spectrometry provides a powerful approach in this area of research.
Biomarker discovery through the application of SWATH-MS
SWATH-MS is a relatively new approach to generating large quantities of reproducible protein expression data. The heterogeneity of human cancers and the unpredictability of drug interventions has made the classification and treatment of this diverse disease very difficult. By combining proteomics datasets acquired using SWATH-MS with whole genome sequencing for a large cohort of patients with clinically characterised disease, we hope to start addressing some of these difficulties.
Research Grants
Understanding the heterogeneity of chronic lymphocytic leukaemia through the elucidation of how genetic alterations influence protein expression at the whole genome level.
NORTH WEST CANCER RESEARCH INCORPORATING CLATTERBRIDGE CANCER RESEARCH (UK)
April 2016 - March 2019
Combined Genetic and Proteomic Screening for early Detection of Pancreatic Cancer.
CANCER RESEARCH UK (UK)
October 2007 - September 2011
Regulated and deregulated secretion from primary myofibroblasts in gastric cancer.
NORTH WEST CANCER RESEARCH FUND
October 2008 - September 2011
Research Collaborations
James Dear
External: Edinburgh University
Plasma biomarkers of drug-induced liver injury
Eithne Costello
Internal
Protein expression profiling in pancreatic cancer and identification of plasma biomarkers capable of distinguishing between cancer, pancreatitis and bile duct obstruction in patients
Andrew Pettitt
Internal
Investigation of chemotherapy resistance in chronic lymphocytic leukaemia (CLL) through proteomic analysis of paired clinical trial samples obtained before treatment and at relapse. In addition, the role of CD40 stimulation in CLL survival and drug response
Ian Prior
Internal
Absolute quantification of Ras isoforms
Andreas Goebel
External: University Hospital Aintree
Molecular mechanisms of CRPS pain