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Stephen John Hill

University of Nottingham - Division of Physiology

United Kingdom

University of Nottingham - Cell Signalling Research Group

SCHOLARLY PAPERS

5

DOWNLOADS

168

TOTAL CITATIONS

0

Scholarly Papers (5)

1.

Monitoring Ligand-Induced Changes in Receptor Conformation with NanoBiT Conjugated Nanobodies

Number of pages: 40 Posted: 21 Apr 2020
University of Nottingham - Division of Physiology, VU University Amsterdam, University of Nottingham, University of Nottingham - Division of Physiology, VU University Amsterdam, University of Nottingham - Division of Physiology and University of Nottingham - Division of Physiology
Downloads 61 (951,658)

Abstract:

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Nanobodies, chemokine receptor, CXCR4, NanoBiT, NanoLuciferase, conformational selectivity, extracellular loop 2.

2.

Probing the Binding of Interleukin-23 to Individual Receptor Components and the IL23 Heteromeric Receptor Complex in Living Cells Using NanoBRET

Number of pages: 48 Posted: 08 Jan 2021
University of Nottingham - Division of Physiology, GlaxoSmithKline - Protein and Cellular Sciences, University of Nottingham - Division of Physiology, University of Nottingham - Division of Physiology, GlaxoSmithKline - Protein and Cellular Sciences, GlaxoSmithKline - Medicine Design, Medicinal Science and Technology and University of Nottingham - Division of Physiology
Downloads 34 (1,263,436)

Abstract:

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Interleukin-23, IL23R, IL12Rβ1, cytokine receptor, receptor oligomerisation, IL23p19, IL12p40, NanoBRET, ligand-binding

3.

The Interleukin-23 Receptor Exists as a Heteromer of IL2Rβ1 and IL23R Under Basal Conditions and Does Not Undergo Ligand-Induced Dimerization on Activation by Cytokine

Number of pages: 29 Posted: 07 Feb 2022
Charles Lay, Peter D. Craggs and Stephen John Hill
University of Nottingham - Division of Physiology, GlaxoSmithKline - Medicine Design, Medicinal Science and Technology and University of Nottingham - Division of Physiology
Downloads 28 (1,345,526)

Abstract:

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Interleukin-23, IL23R, IL12Rβ1, cytokine receptor, receptor oligomerisation, IL23p19, IL12p40, NanoBRET, NanoBiT

4.

NanoB 2: Monitoring Interactions of Ligands with Membrane Proteins by Combining Nanobodies and NanoBRET

Number of pages: 116 Posted: 23 Dec 2022
VU University Amsterdam - Division of Medicinal Chemistry, VU University Amsterdam - Division of Medicinal Chemistry, VU University Amsterdam - Division of Medicinal Chemistry, VU University Amsterdam - Division of Medicinal Chemistry, University of Nottingham - Cell Signalling Research Group, VU University Amsterdam - Division of Medicinal Chemistry, VU University Amsterdam - Division of Medicinal Chemistry, University of Nottingham - Cell Signalling Research Group, University of Nottingham - Division of Bimolecular Science and Medicinal Chemistry, University of Nottingham - Division of Physiology, VU University Amsterdam - Division of Medicinal Chemistry, VU University Amsterdam - Division of Medicinal Chemistry and VU University Amsterdam - Division of Medicinal Chemistry
Downloads 23 (1,411,822)

Abstract:

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GPCRs, RTKs, membrane receptors, NanoBRET, binding, nanobodies, real-time, homogenous, therapeutic potential, fluorescent probes

5.

Probing Ligand-Induced Changes in Cell Surface Expression of E-Selectin Using CRISPR/Cas9-Mediated Protein Tagging with HiBiT in Primary Human Endothelial Cells

Number of pages: 33 Posted: 27 Dec 2022
University of Nottingham - Division of Physiology, University of Nottingham - Division of Physiology, University of Nottingham - Division of Molecular Therapeutics and Formulation, University of Nottingham - Division of Physiology, University of Nottingham - Division of Physiology, University of Nottingham - Division of Physiology and University of Nottingham - Division of Bimolecular Science and Medicinal Chemistry
Downloads 22 (1,424,331)

Abstract:

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NanoLuc, NanoBiT, E-selectin, Inflammatory mediators, E-selectin binding peptide