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De novo design of proteins housing excitonically coupled chlorophyll special pairs.
Ennist, Nathan M; Wang, Shunzhi; Kennedy, Madison A; Curti, Mariano; Sutherland, George A; Vasilev, Cvetelin; Redler, Rachel L; Maffeis, Valentin; Shareef, Saeed; Sica, Anthony V; Hua, Ash Sueh; Deshmukh, Arundhati P; Moyer, Adam P; Hicks, Derrick R; Swartz, Avi Z; Cacho, Ralph A; Novy, Nathan; Bera, Asim K; Kang, Alex; Sankaran, Banumathi; Johnson, Matthew P; Phadkule, Amala; Reppert, Mike; Ekiert, Damian; Bhabha, Gira; Stewart, Lance; Caram, Justin R; Stoddard, Barry L; Romero, Elisabet; Hunter, C Neil; Baker, David.
Afiliação
  • Ennist NM; Institute for Protein Design, University of Washington, Seattle, WA, USA. ennist@uw.edu.
  • Wang S; Department of Biochemistry, University of Washington, Seattle, WA, USA. ennist@uw.edu.
  • Kennedy MA; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Curti M; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Sutherland GA; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Vasilev C; Division of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Redler RL; Institute of Chemical Research of Catalonia (ICIQ-CERCA), Barcelona Institute of Science and Technology (BIST), Tarragona, Spain.
  • Maffeis V; School of Biosciences, University of Sheffield, Sheffield, UK.
  • Shareef S; School of Biosciences, University of Sheffield, Sheffield, UK.
  • Sica AV; Department of Cell Biology and Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY, USA.
  • Hua AS; Institute of Chemical Research of Catalonia (ICIQ-CERCA), Barcelona Institute of Science and Technology (BIST), Tarragona, Spain.
  • Deshmukh AP; Institute of Chemical Research of Catalonia (ICIQ-CERCA), Barcelona Institute of Science and Technology (BIST), Tarragona, Spain.
  • Moyer AP; Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, Tarragona, Spain.
  • Hicks DR; Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, CA, USA.
  • Swartz AZ; Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, CA, USA.
  • Cacho RA; Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, CA, USA.
  • Novy N; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Bera AK; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Kang A; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Sankaran B; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Johnson MP; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Phadkule A; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Reppert M; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Ekiert D; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Bhabha G; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Stewart L; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Caram JR; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Stoddard BL; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Romero E; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Hunter CN; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Baker D; Molecular Biophysics and Integrated Bioimaging, Berkeley Center for Structural Biology, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Nat Chem Biol ; 20(7): 906-915, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38831036
ABSTRACT
Natural photosystems couple light harvesting to charge separation using a 'special pair' of chlorophyll molecules that accepts excitation energy from the antenna and initiates an electron-transfer cascade. To investigate the photophysics of special pairs independently of the complexities of native photosynthetic proteins, and as a first step toward creating synthetic photosystems for new energy conversion technologies, we designed C2-symmetric proteins that hold two chlorophyll molecules in closely juxtaposed arrangements. X-ray crystallography confirmed that one designed protein binds two chlorophylls in the same orientation as native special pairs, whereas a second designed protein positions them in a previously unseen geometry. Spectroscopy revealed that the chlorophylls are excitonically coupled, and fluorescence lifetime imaging demonstrated energy transfer. The cryo-electron microscopy structure of a designed 24-chlorophyll octahedral nanocage with a special pair on each edge closely matched the design model. The results suggest that the de novo design of artificial photosynthetic systems is within reach of current computational methods.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Clorofila Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Clorofila Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos