Abstract
Inositol 1,4,5-trisphosphate (IP3) receptors (IP3R) are intracellular Ca2+ channels. Their opening is initiated by binding of IP3 to the IP3-binding core (IBC; residues 224–604 of IP3R1) and transmitted to the pore via the suppressor domain (SD; residues 1–223). The major conformational changes leading to IP3R activation occur within the N terminus (NT; residues 1–604). We therefore developed a high-throughput fluorescence polarization (FP) assay using a newly synthesized analog of IP3, fluorescein isothiocyanate (FITC)-IP3, to examine the thermodynamics of IP3 and adenophostin A binding to the NT and IBC. Using both single-channel recording and the FP assay, we demonstrate that FITC-IP3 is a high-affinity partial agonist of the IP3R. Conventional [3H]IP3 and FP assays provide similar estimates of the KD for both IP3 and adenophostin A in cytosol-like medium at 4°C. They further establish that the isolated IBC retains the ability of full-length IP3R to bind adenophostin A with ∼10-fold greater affinity than IP3. By examining the reversible effects of temperature on ligand binding, we established that favorable entropy changes (TΔS) account for the greater affinities of both ligands for the IBC relative to the NT and for the greater affinity of adenophostin A relative to IP3. The two agonists differ more substantially in the relative contribution of ΔH and TΔS to binding to the IBC relative to the NT. This suggests that different initial binding events drive the IP3R on convergent pathways toward a similar open state.
Footnotes
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↵ The online version of this article (available at http://molpharm.aspetjournals.org) contains supplemental material.
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This work was supported by the Wellcome Trust [Grants 085295, 082837]; the Biotechnology and Biological Sciences Research Council [Grant BB/E004660]; and the Isaac Newton Trust (Cambridge).
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Article, publication date, and citation information can be found at http://molpharm.aspetjournals.org.
doi:10.1124/mol.109.062596.
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ABBREVIATIONS:
- IP3R
- inositol 1,4,5-trisphosphate receptor
- IBC
- IP3-binding core (residues 224–604 of IP3R1)
- SD
- suppressor domain (residues 1–223 of IP3R1)
- NT
- N-terminal (residues 1–604 of IP3R1)
- FP
- fluorescence polarization
- FITC
- fluorescein 5-isothiocyanate
- GST
- glutathione transferase
- TEAB
- triethylammonium bicarbonate
- TEM
- Tris/EDTA medium
- CLM
- Ca2+-free cytosol-like medium
- PIPES
- piperazine-N,N′-bis(2-ethanesulfonic acid)
- Po
- single channel open probability
- τo
- mean channel open time
- A
- anisotropy
- Bmax
- concentration of binding sites.
- Received November 19, 2009.
- Accepted March 9, 2010.
- Copyright © 2010 The American Society for Pharmacology and Experimental Therapeutics
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