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Protein-specific energy requirements for protein transport across or into thylakoid membranes: Two lumenal proteins are transported in the absence of ATP

*Corresponding author for this work
  • University of Florida
    ,
  • University of California, Davis
Research Output:
Contribution to journal
Article
Peer-review

Abstract

Cytosolically synthesized thylakoid proteins must be translocated across the chloroplast envelope membranes, traverse the stroma, and then be translocated into or across the thylakoid membrane. Protein transport across the envelope requires ATP hydrolysis but not electrical or proton gradients. The energy requirements for the thylakoid translocation step were studied here for the light-harvesting chlorophyll a/b protein (LHCP), an integral membrane protein, and for several thylakoid lumen-resident proteins: plastocyanin and OE33, OE23, and OE17 (the 33-, 23-, and 17-kDa subunits of the oxygen-evolving complex, respectively). Dissipation of the thylakoid protonmotive force during an in organello protein import assay partially inhibited the thylakoid localization of LHCP and OE33, totally inhibited localization of OE23 and OE17, and had no effect on localization of plastocyanin. We used reconstitution assays for LHCP insertion and for OE23 and OE17 transport into isolated thylakoids to investigate the energy requirements in detail. The results indicated that LHCP insertion absolutely requires ATP hydrolysis and is enhanced by a transthylakoid ΔpH and that transport of OE23 and OE17 is absolutely dependent upon a ΔpH. Surprisingly, OE23 and OE17 transport occurred maximally in the complete absence of ATP. These results establish the thylakoid membrane as the only membrane system in which a ΔpH can provide all of the energy required to translocate proteins across the bilayer. They also demonstrate that the energy requirements for integration into or translocation across the thylakoid membranes are protein-specific.

Bibliographic Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 2688-2696 (9 pages)

Journal (Volume, Issue Number)

Journal of Biological Chemistry (Volume 267, Issue 4)

Publication milestones

  • Published - 05/02/1992

Publication status

Published - 05/02/1992

ISSN

0021-9258

Publication IDs

  • Scopus: 0026787702
  • PubMed: 1733965