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Central functions of the lumenal and peripheral thylakoid proteome of Arabidopsis determined by experimentation and genome-wide prediction

Peltier, Jean-Benoît (författare)
Emanuelsson, Olof (författare)
Stockholms universitet
Kalume, Dário E. (författare)
visa fler...
Ytterberg, Jimmy (författare)
Friso, Giulia (författare)
Rudella, Andrea (författare)
Liberles, David A. (författare)
Söderberg, Linda (författare)
Roepstorff, Peter (författare)
von Heijne, Gunnar (författare)
van Wijk, Klaas J (författare)
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 (creator_code:org_t)
2002-01-01
2002
Engelska.
Ingår i: The Plant Cell. - : Oxford University Press (OUP). - 1040-4651 .- 1532-298X. ; 14:1, s. 211-236
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Experimental proteome analysis was combined with a genome-wide prediction screen to characterize the protein content of the thylakoid lumen of Arabidopsis chloroplasts. Soluble thylakoid proteins were separated by two-dimensional electrophoresis and identified by mass spectrometry. The identities of 81 proteins were established, and N termini were sequenced to validate localization prediction. Gene annotation of the identified proteins was corrected by experimental data, and an interesting case of alternative splicing was discovered. Expression of a surprising number of paralogs was detected. Expression of five isomerases of different classes suggests strong (un)folding activity in the thylakoid lumen. These isomerases possibly are connected to a network of peripheral and lumenal proteins involved in antioxidative response, including peroxiredoxins, m-type thioredoxins, and a lumenal ascorbate peroxidase. Characteristics of the experimentally identified lumenal proteins and their orthologs were used for a genome-wide prediction of the lumenal proteome. Lumenal proteins with a typical twin-arginine translocation motif were predicted with good accuracy and sensitivity and included additional isomerases and proteases. Thus, prime functions of the lumenal proteome include assistance in the folding and proteolysis of thylakoid proteins as well as protection against oxidative stress. Many of the predicted lumenal proteins must be present at concentrations at least 10,000-fold lower than proteins of the photosynthetic apparatus.

Ämnesord

NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)

Nyckelord

SEC-INDEPENDENT INSERTION
PH-DEPENDENT PATHWAY
DISULFIDE-ISOMERASE
MASS-SPECTROMETRY
CHLAMYDOMONAS-REINHARDTII
2-CYSTEINE PEROXIREDOXIN
ASCORBATE PEROXIDASE
POLYACRYLAMIDE-GELS
MEMBRANE-PROTEINS
SIGNAL PEPTIDES

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