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mTOR direct interactions with Rheb-GTPase and raptor: sub-cellular localization using fluorescence lifetime imaging

mTOR direct interactions with Rheb-GTPase and raptor: sub-cellular localization using fluorescence lifetime imaging
mTOR direct interactions with Rheb-GTPase and raptor: sub-cellular localization using fluorescence lifetime imaging
Background: The mammalian target of rapamycin (mTOR) signalling pathway has a key role in cellular regulation and several diseases. While it is thought that Rheb GTPase regulates mTOR, acting immediately upstream, while raptor is immediately downstream of mTOR, direct interactions have yet to be verified in living cells, furthermore the localisation of Rheb has been reported to have only a cytoplasmic cellular localization.

Results: In this study a cytoplasmic as well as a significant sub-cellular nuclear mTOR localization was shown , utilizing green and red fluorescent protein (GFP and DsRed) fusion and highly sensitive single photon counting fluorescence lifetime imaging microscopy (FLIM) of live cells. The interaction of the mTORC1 components Rheb, mTOR and raptor, tagged with EGFP/DsRed was determined using fluorescence energy transfer-FLIM. The excited-state lifetime of EGFP-mTOR of ~2400 ps was reduced by energy transfer to ~2200 ps in the cytoplasm and to 2000 ps in the nucleus when co-expressed with DsRed-Rheb, similar results being obtained for co-expressed EGFP-mTOR and DsRed-raptor. The localization and distribution of mTOR was modified by amino acid withdrawal and re-addition but not by rapamycin.

Conclusions: The results illustrate the power of GFP-technology combined with FRET-FLIM imaging in the study of the interaction of signalling components in living cells, here providing evidence for a direct physical interaction between mTOR and Rheb and between mTOR and raptor in living cells for the first time.
3
Yadav, Rahul B.
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Burgos, Pierre
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Parker, Anthony W.
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Iadevaia, Valentina
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Proud, Christopher G.
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Allen, Rodger A.
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O'Connell, James P.
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Jeshtadi, Ananya
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Stubbs, Christopher D.
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Botchway, Stanley W.
bd1cc68e-124c-4e7f-a022-b286791edcfc
Yadav, Rahul B.
86c6411f-0fce-4da8-a8a7-5a65b76e72eb
Burgos, Pierre
1ec95bec-014f-491c-886b-c3014817da62
Parker, Anthony W.
9b5a0329-1ffe-4595-b330-861677c0e9f0
Iadevaia, Valentina
1124252e-5709-4a5e-8a4b-956ced0c9611
Proud, Christopher G.
59dabfc8-4b44-4be8-a17f-578a58550cb3
Allen, Rodger A.
d8716211-0fa9-474d-b860-afb99201d175
O'Connell, James P.
a503ece4-ca73-477e-b75b-b182947e86f7
Jeshtadi, Ananya
5b15295d-74a7-4aaa-984e-88bdbc328103
Stubbs, Christopher D.
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Botchway, Stanley W.
bd1cc68e-124c-4e7f-a022-b286791edcfc

Yadav, Rahul B., Burgos, Pierre, Parker, Anthony W., Iadevaia, Valentina, Proud, Christopher G., Allen, Rodger A., O'Connell, James P., Jeshtadi, Ananya, Stubbs, Christopher D. and Botchway, Stanley W. (2013) mTOR direct interactions with Rheb-GTPase and raptor: sub-cellular localization using fluorescence lifetime imaging. BMC Cell Biology, 14 (1), 3. (doi:10.1186/1471-2121-14-3). (PMID:23311891)

Record type: Article

Abstract

Background: The mammalian target of rapamycin (mTOR) signalling pathway has a key role in cellular regulation and several diseases. While it is thought that Rheb GTPase regulates mTOR, acting immediately upstream, while raptor is immediately downstream of mTOR, direct interactions have yet to be verified in living cells, furthermore the localisation of Rheb has been reported to have only a cytoplasmic cellular localization.

Results: In this study a cytoplasmic as well as a significant sub-cellular nuclear mTOR localization was shown , utilizing green and red fluorescent protein (GFP and DsRed) fusion and highly sensitive single photon counting fluorescence lifetime imaging microscopy (FLIM) of live cells. The interaction of the mTORC1 components Rheb, mTOR and raptor, tagged with EGFP/DsRed was determined using fluorescence energy transfer-FLIM. The excited-state lifetime of EGFP-mTOR of ~2400 ps was reduced by energy transfer to ~2200 ps in the cytoplasm and to 2000 ps in the nucleus when co-expressed with DsRed-Rheb, similar results being obtained for co-expressed EGFP-mTOR and DsRed-raptor. The localization and distribution of mTOR was modified by amino acid withdrawal and re-addition but not by rapamycin.

Conclusions: The results illustrate the power of GFP-technology combined with FRET-FLIM imaging in the study of the interaction of signalling components in living cells, here providing evidence for a direct physical interaction between mTOR and Rheb and between mTOR and raptor in living cells for the first time.

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Published date: January 2013
Organisations: Centre for Biological Sciences

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Local EPrints ID: 350247
URI: http://eprints.soton.ac.uk/id/eprint/350247
PURE UUID: 08751b75-1849-43cc-9bab-6361aa8d831a

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Date deposited: 20 Mar 2013 12:25
Last modified: 14 Mar 2024 13:23

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Contributors

Author: Rahul B. Yadav
Author: Pierre Burgos
Author: Anthony W. Parker
Author: Valentina Iadevaia
Author: Christopher G. Proud
Author: Rodger A. Allen
Author: James P. O'Connell
Author: Ananya Jeshtadi
Author: Christopher D. Stubbs
Author: Stanley W. Botchway

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