Dr James E Pease

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Dr James E Pease

Reader in Leukocyte Biology
National Heart & Lung Institute

Tel: +44 (0)20 7594 3162
Email: Email address for Dr James E Pease

Dr James E Pease

James Pease is a Reader in Leukocyte Biology within the Leukocyte Biology Section of the National Heart and Lung Institute of Imperial College and is a principal investigator  within the Medical Research Council/Asthma UK Centre in Allergic Mechanisms of Asthma and the British Heart Foundation Centre of Research Excellence.

James completed his BSc in Biochemistry at the University of Manchester before moving to the University of Sheffield where he studied for a PhD in the Department of Molecular Biology and Biotechnology.  His PhD thesis concerned the characterization of the cell surface receptor for the complement fragment C5a and lead to a keen interest in the role of G protein-coupled receptors (GPCRs) involved in immunity.  After completing a 4-year post-doctoral stint within the same department at the University of Sheffield, James moved to the laboratory of Dr Philip Murphy at the National Institutes of Health in Bethesda, Maryland, where he commenced studies on the recently discovered family of chemokine receptors.  There he developed methodologies to examine the structure/function relationships of the receptors, identifying key domains of the proteins which were involved in binding both chemokine ligands and also HIV-1 envelope proteins.

James moved back to the UK in 1997 to the recently formed Leukocyte Biology Section within the NHLI Division of Imperial College London.  There his interests included the identification of binding sites of prototypic small molecule antagonists of chemokine receptors with obvious therapeutic potential in a wide range of diseases.  Current research interests of the group include other aspects of chemokine biology including regulation and trafficking of receptors, their role in disease and also the efforts of microbes to circumvent the chemokine system. Funding for the research comes from Arthritis UK, BBSRC, British Heart Foundation, MRC, Wellcome Trust and collaborations with pharmaceutical companies both in the UK and abroad.

James makes a significant contribution to undergraduate teaching within the Faculty of Medicine and was awarded his Certificate in Advanced Studies in Learning and Teaching by the college in 2002. He is currently Deputy Theme leader of the Molecules, Cells and Disease of the year 1 MBBS programme and also acts as course leader for the metabolism component. He is a member of the MRC College of Experts and also sits on the editorial board of the publications Journal of Innate Immunity and Inflammation & Allergy – Drug Targets.

 

Selected Publications


Journals

  • Wise EL; Bonner KT; Williams TJ; Pease JE. (Jul 2010). A single nucleotide polymorphism in the CCR3 gene ablates receptor export to the plasma membrane. J Allergy Clin Immunol. 126:150-7.e2. DOI.
  • Meiser A; Mueller A; Wise EL; McDonagh EM; Petit SJ; Saran N; Clark PC; Williams TJ; et alPease JE. (15 May 2008). The chemokine receptor CXCR3 is degraded following internalization and is replenished at the cell surface by de novo synthesis of receptor. JOURNAL OF IMMUNOLOGY. 180:6713-6724. Author weblink.
  • Wise EL; Duchesnes C; da Fonseca PCA; Allen RA; Williams TJ; Pease JE. (21 Sep 2007). Small molecule receptor agonists and antagonists of CCR3 provide insight into mechanisms of chemokine receptor activation. JOURNAL OF BIOLOGICAL CHEMISTRY. 282:27935-27943. Author weblink DOI.
  • Pease JE; Williams TJ. (1 Aug 2006). Chemokines and their receptors in allergic disease. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 118:305-318. Author weblink DOI.
  • Sabroe I; Peck MJ; Van Keulen BJ; Jorritsma A; Simmons G; Clapham PR; Williams TJ; Pease JE. (25 Aug 2000). A small molecule antagonist of chemokine receptors CCR1 and CCR3. Potent inhibition of eosinophil function and CCR3-mediated HIV-1 entry. J Biol Chem. 275:25985-25992. DOI.
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