Kirk Taylor

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100
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Lecturer
Areas of interest
Kirk is interested in all aspects of platelet and megakaryocyte, with particular focus on the role of ion channels in regulating pathological thrombus formation. His PhD studies focussed on the role of platelet Pannexin-1 channels and electrophysiological characterisation of megakaryocyte TMEM16F channels. Kirk has developed assays to evaluate platelet function responses in clinical trials evaluating the pharmacokinetic profiles of HIV therapeutics.
Expertise
Biochemical (immunohistochemistry, Western blotting), biophysical (whole-cell patch clamp), cell isolation & culture (platelet & primary MK isolation and cell culture), functional (aggregometry, Ca2+ imaging, flow cytometry, ATP release & dye efflux), imaging (confocal and fluorescence microscopy), in vivo (cardiac puncture, vessel cannulation, tissue isolation) and molecular (cloning, PCR) assays.
Research centres and groups
- Member of the Platelet Society executive Committee
- Serves on the editorial board of the journal Platelets as social media and Equality, Diversity & Inclusion Officer.
- He is also actively engaged in public engagement initiatives, such as Pint of Science and LGBT STEM Day.
Background
Kirk completed his PhD at the University of Leicester under the mentorship of Prof Mahaut-Smith. His studies focussed on the role of ion channels in regulating platelet and megakaryocyte function. He has completed postdoctoral posts at Anglia Ruskin University (Dr Nick Pugh) and Imperial College London (Dr Mike Emerson) studying mechanisms of zinc-induced platelet activation and pharmacological effects of HIV therapies upon platelet function, respectively. Kirk joined the ÌÇÐÄ̽»¨ Platelet Lab to investigate the role of platelet and megakaryocyte gap junction proteins in regulating blood clot formation. Kirk has previously secured funding from the Wellcome Trust and National Heart and Lung Institute to evaluate the therapeutic potential of ion channels in platelet-related disorders.Awards and honours
- NHLI Pilot Award; Imperial College London, 2020 (PI: £4,615)
- British Heart Foundation Small Meeting Fund; (Co-applicant: £1,900)
- Wellcome Trust Vacation Scholarship; Imperial College London, 2019 (Co-I: £2,768)
- Wellcome Trust Vacation Scholarship; Anglia Ruskin University, 2016 (Co-I: £2,768)
- Best Oral Presentation; UK Platelet Society, Manchester Metropolitan University, 2018 (£100)
- Travel scholarships (£5,648)
Websites/blogs
Connections
Selected publications
- Boustani K & Taylor KA (2020). Navigating LGBTQ+ discrimination in academia: where do we go from here? The Biochemist. .
- Taylor KA & Machlus KR (2020). Blood and Bone: The Quarantine Chronicles. Research and Practice in Thrombosis and Haemostasis. .
- ≠Taylor KA & Mahaut-Smith MP (2019). Whole cell recordings of megakaryocyte Ca2+ activated currents sensitive to the TMEM16F inhibitor CaCCinh-A01 reveal an interspecies difference in ionic selectivity. Platelets. 22:1-5
- Taylor KA, Smyth E, Rauzi F, Cerrone M, Khawaja AA, Gazzard B, Nelson M, Boffito M & Emerson M (2019). Pharmacological impact of antiretroviral therapy on platelet function to investigate human immunodeficiency virus-associated cardiovascular risk. Br J Pharmacol. 176(7):879-889.
- Ahmed NS, Lopes-Pires ME, Taylor KA & Pugh N (2019). Agonist-evoked increases in intra-platelet zinc couple to functional responses. Thromb Haemost. 119(1):128-139.
- Taylor KA & Emerson, M (2018). Refinement of a mouse cardiovascular model: Development, application and dissemination. F1000res, 7: 593
- Gillespie S, Holloway PM, Becker F, Rauzi F, Vital SA, Taylor KA, Stokes KY, Emerson M & Gavins FNE (2018). The isothiocyanate sulforaphane modulates platelet function and protects against cerebral thrombotic dysfunction. Br J. Pharm.; 175(16): 3333-3346
- *Taylor KA, Wilson DGS, Harper MT & Pugh N (2017). Extracellular chloride is required for efficient platelet aggregation. Platelets; 29(1): 79-83
- Pugh N, Maddox B, Bihan D, Taylor KA, Mahaut-Smith MP & Farndale RW (2017). Discrete platelet collagen receptor engagement differentially influences intracellular calcium signalling, integrin activation and thrombus morpholog