Dr Roz Jenkins BSc (Hons), PhD

Research Fellow and Lab Manager, CDSS/ITM Proteomics Facility Pharmacology & Therapeutics

    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