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Dissection of Local Ca2+ Signals in Cultured Cells by Membrane-targeted Ca2+ Indicators
Published on: March 22, 2019
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A canonical EF-loop directs Ca(2+) -sensitivity in phospholipase C-η2
Petra Popovics1, Jin Lu, L Nadia Kamil
1School of Medicine, University of St Andrews, St Andrews, UK.
Journal of Cellular Biochemistry
|October 15, 2013
Summary
Phospholipase C-η2 (PLCη2) uses its EF-hand domain to sense calcium (Ca2+), with EF-loop 1 being crucial for this function. EF-loop 2 does not appear to be involved in Ca2+ sensing by PLCη2.
Area of Science:
- Biochemistry
- Molecular Biology
- Cell Signaling
Background:
- Phospholipase C-η (PLCη) enzymes hydrolyze phosphatidylinositol 4,5-bisphosphate, playing a role in intracellular signaling.
- PLCη2 exhibits calcium (Ca2+) sensitivity, suggesting a role in amplifying transient Ca2+ signals.
- PLCη enzymes feature an EF-hand domain with a canonical EF-loop 1 and a non-canonical EF-loop 2.
Purpose of the Study:
- To investigate the role of the EF-hand domain in PLCη2's Ca2+ sensing capabilities.
- To determine which EF-loop within the EF-hand domain is responsible for Ca2+ binding and signal transduction.
- To elucidate the mechanism by which PLCη2 responds to changes in intracellular Ca2+ levels.
Main Methods:
- 2D-[(1)H,(1)H] TOCSY NMR was used to examine Ca2+ binding to synthetic peptides of PLCη2 EF-loops and calmodulin.
- Molecular modeling was employed to construct a model of the PLCη2 EF-hand domain based on calmodulin structure.
- Inositol phosphate accumulation assays were performed in COS7 cells expressing wild-type and mutant PLCη2 proteins to measure enzyme activity and Ca2+ sensitivity.
Main Results:
- Both PLCη2 EF-loop peptides bound Ca2+ similarly to calmodulin EF-loop 1, particularly at the N-terminus.
- Wild-type PLCη2 activity increased 4- to 7-fold with monensin-induced intracellular Ca2+ elevation and showed a ~4-fold increase at 1 µM free Ca2+.
- A D256A mutation in EF-loop 1 significantly reduced Ca2+ sensitivity by ~10-fold and abolished monensin response, confirming EF-loop 1's role in Ca2+ sensing.
- Mutations in EF-loop 2 (D292A, H296A, Q297A, E304A) did not significantly affect monensin response or Ca2+ sensitivity, indicating EF-loop 2 is not involved in Ca2+ sensing.
Conclusions:
- The EF-hand domain of PLCη2 is critical for its ability to sense intracellular Ca2+ levels.
- EF-loop 1 of the PLCη2 EF-hand domain is the primary Ca2+-binding site responsible for mediating Ca2+ sensitivity.
- The non-canonical EF-loop 2 does not play a significant role in the Ca2+-sensing mechanism of PLCη2.
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