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Insertion of PsaK into the Thylakoid membrane in a "Horseshoe" conformation occurs in the absence of signal recognition particle, nucleoside triphosphates, or functional albino3

Insertion of PsaK into the Thylakoid membrane in a "Horseshoe" conformation occurs in the absence of signal recognition particle, nucleoside triphosphates, or functional albino3
Insertion of PsaK into the Thylakoid membrane in a "Horseshoe" conformation occurs in the absence of signal recognition particle, nucleoside triphosphates, or functional albino3

The photosystem I subunit PsaK spans the thylakoid membrane twice, with the N and C termini both located in the lumen. The insertion mechanism of a thylakoid membrane protein adopting this type of topology has not been studied before, and we have used in vitro assays to determine the requirements for PsaK insertion into thylakoids. PsaK inserts with high efficiency and we show that one transmembrane span (the C-terminal region) can insert independently of the other, indicating that a "hairpin"-type mechanism is not essential. Insertion of PsaK does not require stromal extract, indicating that signal recognition particle (SRP) is not involved. Removal of nucleoside triphosphates inhibits insertion only slightly, both in the presence and absence of stroma, suggesting a mild stimulatory effect of a factor in the translation system and again ruling out an involvement of SRP or its partner protein, FtsY. We, furthermore, find no evidence for the involvement of known membrane-bound translocation apparatus; proteolysis of thylakoids destroys the Sec and Tat translocons but does not block PsaK insertion, and antibodies against the Oxa1/YidC homolog, Alb3, block the SRP-dependent insertion of Lhcb1 but again have no effect on PsaK insertion. Because YidC is required for the efficient insertion of every membrane protein tested in Escherichia coli (whether SRP-dependent or -independent), PsaK is the first protein identified as being independent of YidC/Alb3-type factors in either thylakoids or bacteria. The data raise the possibility of a wholly spontaneous insertion pathway.

0021-9258
36200-36206
Mant, Alexandra
63319e45-deeb-45ad-a30d-e05b42052a0d
Woolhead, Cheryl A.
8107283b-4e29-4dff-be86-4798ee40d5df
Moore, Misty
49c13654-0b50-4d86-985e-4d12cd83004e
Henry, Ralph
9b49c6f0-a0e5-459a-a223-420f44f85236
Robinson, Colin
678e0157-d628-44e8-83de-3591b07c673f
Mant, Alexandra
63319e45-deeb-45ad-a30d-e05b42052a0d
Woolhead, Cheryl A.
8107283b-4e29-4dff-be86-4798ee40d5df
Moore, Misty
49c13654-0b50-4d86-985e-4d12cd83004e
Henry, Ralph
9b49c6f0-a0e5-459a-a223-420f44f85236
Robinson, Colin
678e0157-d628-44e8-83de-3591b07c673f

Mant, Alexandra, Woolhead, Cheryl A., Moore, Misty, Henry, Ralph and Robinson, Colin (2001) Insertion of PsaK into the Thylakoid membrane in a "Horseshoe" conformation occurs in the absence of signal recognition particle, nucleoside triphosphates, or functional albino3. The Journal of Biological Chemistry, 276 (39), 36200-36206. (doi:10.1074/jbc.M102914200).

Record type: Article

Abstract

The photosystem I subunit PsaK spans the thylakoid membrane twice, with the N and C termini both located in the lumen. The insertion mechanism of a thylakoid membrane protein adopting this type of topology has not been studied before, and we have used in vitro assays to determine the requirements for PsaK insertion into thylakoids. PsaK inserts with high efficiency and we show that one transmembrane span (the C-terminal region) can insert independently of the other, indicating that a "hairpin"-type mechanism is not essential. Insertion of PsaK does not require stromal extract, indicating that signal recognition particle (SRP) is not involved. Removal of nucleoside triphosphates inhibits insertion only slightly, both in the presence and absence of stroma, suggesting a mild stimulatory effect of a factor in the translation system and again ruling out an involvement of SRP or its partner protein, FtsY. We, furthermore, find no evidence for the involvement of known membrane-bound translocation apparatus; proteolysis of thylakoids destroys the Sec and Tat translocons but does not block PsaK insertion, and antibodies against the Oxa1/YidC homolog, Alb3, block the SRP-dependent insertion of Lhcb1 but again have no effect on PsaK insertion. Because YidC is required for the efficient insertion of every membrane protein tested in Escherichia coli (whether SRP-dependent or -independent), PsaK is the first protein identified as being independent of YidC/Alb3-type factors in either thylakoids or bacteria. The data raise the possibility of a wholly spontaneous insertion pathway.

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Published date: 28 September 2001

Identifiers

Local EPrints ID: 414028
URI: http://eprints.soton.ac.uk/id/eprint/414028
ISSN: 0021-9258
PURE UUID: 836dbabc-f100-4b1b-829b-750fda6038c1
ORCID for Alexandra Mant: ORCID iD orcid.org/0000-0001-7169-209X

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Date deposited: 12 Sep 2017 16:32
Last modified: 16 Mar 2024 03:40

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Contributors

Author: Alexandra Mant ORCID iD
Author: Cheryl A. Woolhead
Author: Misty Moore
Author: Ralph Henry
Author: Colin Robinson

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