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Updated: Jun 14, 2026

Profiling Thiol Redox Proteome Using Isotope Tagging Mass Spectrometry
Published on: March 24, 2012
Differential proteomic analysis using iTRAQ reveals changes in thylakoids associated with Photosystem II-acquired
John G Rowland1, William J Simon, Yoshitaka Nishiyama
1School of Biological and Biomedical Sciences, University of Durham, Durham, UK.
Abstract:
Growth temperature has a marked influence on the thermotolerance of photosystem II (PSII), which is the most heat-sensitive component of photosynthesis. Using Synechocystis sp. PCC 6803 we have established that thylakoids isolated from cells grown at 38 degrees C have a greater degree of thermotolerance than those isolated from cells grown at 25 degrees C. Reconstitution experiments using Triton X-100 protein extracts of these thylakoids added to Triton-treated thylakoid membranes further indicated that the 38 degrees C Triton extract contains proteins that are directly capable of enhancing PSII thermotolerance. We have used 4-plex iTRAQ, extensive off-line fractionation and sample re-injection to comprehensively identify the differences between these two preparations that may be responsible for the observed effects on PSII thermotolerance. This has resulted in the reproducible identification of 168 proteins out of a total of 385 distinct proteins. Our results have identified 15 proteins whose levels are increased in extracts that result in increased thermotolerance of PSII and 33 proteins whose levels decrease. Notably, components of the cytochrome b(6)/f and NADH dehydrogenase complexes, crucial components in electron transport, are approximately twofold more abundant in 38 degrees C thylakoid extracts. The possible biological importance of these changes is discussed.
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