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Photoactivation Mechanism, Timing of Protein Secondary Structure Dynamics and Carotenoid Translocation in the Orange Carotenoid Protein.
Konold, Patrick E; van Stokkum, Ivo H M; Muzzopappa, Fernando; Wilson, Adjélé; Groot, Marie-Louise; Kirilovsky, Diana; Kennis, John T M.
Afiliación
  • Konold PE; Department of Physics and Astronomy, Faculty of Sciences , Vrije Universiteit , De Boelelaan 1081 , 1081HV Amsterdam , The Netherlands.
  • van Stokkum IHM; Department of Physics and Astronomy, Faculty of Sciences , Vrije Universiteit , De Boelelaan 1081 , 1081HV Amsterdam , The Netherlands.
  • Muzzopappa F; Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS , Universite Paris-Sud, Universite Paris-Saclay , 91198 Gif-sur-Yvette , France.
  • Wilson A; Institut Joliot , Commissariat a l'Energie Atomique (CEA) , 91191 Gif-sur-Yvette , France.
  • Groot ML; Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS , Universite Paris-Sud, Universite Paris-Saclay , 91198 Gif-sur-Yvette , France.
  • Kirilovsky D; Institut Joliot , Commissariat a l'Energie Atomique (CEA) , 91191 Gif-sur-Yvette , France.
  • Kennis JTM; Department of Physics and Astronomy, Faculty of Sciences , Vrije Universiteit , De Boelelaan 1081 , 1081HV Amsterdam , The Netherlands.
J Am Chem Soc ; 141(1): 520-530, 2019 01 09.
Article en En | MEDLINE | ID: mdl-30511841
ABSTRACT
The orange carotenoid protein (OCP) is a two-domain photoactive protein that noncovalently binds an echinenone (ECN) carotenoid and mediates photoprotection in cyanobacteria. In the dark, OCP assumes an orange, inactive state known as OCPO; blue light illumination results in the red active state, known as OCPR. The OCPR state is characterized by large-scale structural changes that involve dissociation and separation of C-terminal and N-terminal domains accompanied by carotenoid translocation into the N-terminal domain. The mechanistic and dynamic-structural relations between photon absorption and formation of the OCPR state have remained largely unknown. Here, we employ a combination of time-resolved UV-visible and (polarized) mid-infrared spectroscopy to assess the electronic and structural dynamics of the carotenoid and the protein secondary structure, from femtoseconds to 0.5 ms. We identify a hereto unidentified carotenoid excited state in OCP, the so-called S* state, which we propose to play a key role in breaking conserved hydrogen-bond interactions between carotenoid and aromatic amino acids in the binding pocket. We arrive at a comprehensive reaction model where the hydrogen-bond rupture with conserved aromatic side chains at the carotenoid ß1-ring in picoseconds occurs at a low yield of <1%, whereby the ß1-ring retains a trans configuration with respect to the conjugated π-electron chain. This event initiates structural changes at the N-terminal domain in 1 µs, which allow the carotenoid to translocate into the N-terminal domain in 10 µs. We identified infrared signatures of helical elements that dock on the C-terminal domain ß-sheet in the dark and unfold in the light to allow domain separation. These helical elements do not move within the experimental range of 0.5 ms, indicating that domain separation occurs on longer time scales, lagging carotenoid translocation by at least 2 decades of time.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Carotenoides / Luz Idioma: En Revista: J Am Chem Soc Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Carotenoides / Luz Idioma: En Revista: J Am Chem Soc Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos