2001
DOI: 10.1083/jcb.200105149
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Thylakoid ΔpH-dependent precursor proteins bind to a cpTatC–Hcf106 complex before Tha4-dependent transport

Abstract: The thylakoid ΔpH-dependent pathway transports folded proteins with twin arginine–containing signal peptides. Identified components of the machinery include cpTatC, Hcf106, and Tha4. The reaction occurs in two steps: precursor binding to the machinery, and transport across the membrane. Here, we show that a cpTatC–Hcf106 complex serves as receptor for specific binding of twin arginine–containing precursors. Antibodies to either Hcf106 or cpTatC, but not Tha4, inhibited precursor binding. Blue native gel electr… Show more

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Cited by 264 publications
(368 citation statements)
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“…Imported Tha4 migrated at 240 kDa (lane 3). These are the same profiles obtained for endogenous components solubilized under comparable conditions [8].…”
Section: Association Of In Vitro Translated Components With Endogenousupporting
confidence: 77%
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“…Imported Tha4 migrated at 240 kDa (lane 3). These are the same profiles obtained for endogenous components solubilized under comparable conditions [8].…”
Section: Association Of In Vitro Translated Components With Endogenousupporting
confidence: 77%
“…Lanes were loaded with enriched fractions on an equal protein basis (lanes 1-4) and also in the approximate stoichiometric ratio that these membranes are present in chloroplasts (lanes 5-8). Both Tha4 and Hcf106 are primarily localized in thylakoids (lanes [5][6][7][8] but are also present in envelope fractions. This is especially apparent when equal amounts of protein are compared (lanes [1][2][3][4].…”
Section: Resultsmentioning
confidence: 99%
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