4.4 Article

A practical process for the preparation of [P-32]S1P and binding assay for S1P receptor ligands

Journal

APPLIED RADIATION AND ISOTOPES
Volume 102, Issue -, Pages 5-9

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.apradiso.2015.04.010

Keywords

Competitive binding assay; Phosphorus-32; Radioligand; Sphingosine 1-phosphate; Sphingosine 1-phosphate Receptors; Sphingosine kinase 1

Funding

  1. Department of Energy [DESC0008432]
  2. National Institute of Neurological Disorders and Stroke (NINDS) [R01NS075527]
  3. National Institute of Mental Health (NIMH) of the National Institutes of Health [MH092797]
  4. NATIONAL INSTITUTE OF MENTAL HEALTH [R33MH092797, R21MH092797] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R21NS061025, R01NS075527] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Sphingosine-1-phosphate receptors (S1PRs) are important regulators of vascular permeability, inflammation, angiogenesis and vascular maturation. Identifying a specific S1PR PET radioligand is imperative, but it is hindered by the complexity and variability of current for binding affinity measurement procedures. Herein, we report a streamlined protocol for radiosynthesis of [P-32]S1P with good radiochemical yield (36-50%) and high radiochemical purity (>99%). We also report a reproducible procedure for determining the binding affinity for compounds targeting S1PRs in vitro. (C) 2015 Elsevier Ltd. All rights reserved.

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