Crystal structure of Psb31, a novel extrinsic protein of photosystem II from a marine centric diatom and implications for its binding and function

Ryo Nagao, Michihiro Suga, Ayako Niikura, Akinori Okumura, Faisal Hammad Mekky Koua, Takehiro Suzuki, Tatsuya Tomo, Isao Enami, Jian Ren Shen

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

Psb31 is a fifth extrinsic protein found in photosystem II (PSII) of a centric diatom, Chaetoceros gracilis. The protein has been shown to bind directly to PSII in the absence of other extrinsic proteins and serves in part as a substitute for PsbO in supporting oxygen evolution. We report here the crystal structure of Psb31 at a resolution of 1.55 Å. The structure of Psb31 was composed of two domains, one major, N-terminal four helical domain and one minor, flexible C-terminal domain. The four helices in the N-terminal domain were arranged in an up-down-up-down fold, which appeared unexpectedly to be similar to the structure of spinach PsbQ, in spite of their low sequence homology. This suggests that the centric diatom PSII contains another PsbQ-type extrinsic protein in addition to the original PsbQ protein found in the organism. On the other hand, the C-terminal domain of Psb31 has a unique structure composed of one loop and one short helix. Based on these structural analysis and chemical cross-linking experiments, residues responsible for the binding of Psb31 to PSII intrinsic proteins were suggested. The results are discussed in relation to the copy number of extrinsic proteins in higher plant PSII.

Original languageEnglish
Pages (from-to)6646-6652
Number of pages7
JournalBiochemistry
Volume52
Issue number38
DOIs
Publication statusPublished - Sept 24 2013

ASJC Scopus subject areas

  • Biochemistry

Fingerprint

Dive into the research topics of 'Crystal structure of Psb31, a novel extrinsic protein of photosystem II from a marine centric diatom and implications for its binding and function'. Together they form a unique fingerprint.

Cite this