Ultrafast infrared spectroscopy reveals a key step for successful entry into the photocycle for photoactive yellow protein

L. van Wilderen, M.A. Horst, K.J. Hellingwerf, I.H.M. van Stokkum, R. van Grondelle, M.L. Groot

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Photoactive proteins such as PYP (photoactive yellow protein) are generally accepted as model systems for studying protein signal state formation. PYP is a blue-light sensor from the bacterium Halorhodospira halophila. The formation of PYP's signaling state is initiated by trans-cis isomerization of the p-coumaric acid chromophore upon the absorption of light. The quantum yield of signaling state formation is ≈0.3. Using femtosecond visible pump/mid-IR probe spectroscopy, we investigated the structure of the very short-lived ground state intermediate (GSI) that results from an unsuccessful attempt to enter the photocycle. This intermediate and the first stable GSI on pathway into the photocycle, I
Original languageEnglish
Pages (from-to)15050-15055
JournalProceedings of the National Academy of Sciences of the United States of America
Volume103
Issue number41
DOIs
Publication statusPublished - 2006

Bibliographical note

Ultrafast infrared spectroscopy reveals a key step for successful entry into the photocycle for photoactive yellow protein

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