Excimer and non-photochemical quenching in LHCII

J Jian-Wei Zou (College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,) D Dan-Hong Li (College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,) R Rong-Yao Gao (Key Laboratory of Advanced Light Conversion Materials and Biophotonics, Department of Chemistry and Life Resources, Renmin University of China 3 , Beijing 100872,) Y Yu-Qian Li (Key Laboratory of Advanced Light Conversion Materials and Biophotonics, Department of Chemistry and Life Resources, Renmin University of China 3 , Beijing 100872,) Q Qi-Rui Yu (College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,) Z Zhi-Hao Yu (College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,) A Alexander V. Ruban (Department of Biochemistry, School of Biological and Behavioural Sciences, Queen Mary University of London 2 , London E1 4NS,) J Jian-Ping Zhang J Junrong Zheng (College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,)

Abstract

The light-harvesting complex of photosystem II (LHCII) plays the dual roles of photosynthetic energy capture and dissipation, where the excitation energy in excess is dissipated safely via non-photochemical quenching (NPQ) to avoid photodamage. Chlorophyll excimer was recently reported to be an intrinsic photophysical intermediate in LHCII, which may serve as an efficient quencher of Chl singlet excitation (1Chl*). We have employed ultrafast transient absorption and broadband two-dimensional electronic spectroscopy to investigate the mechanism of 1Chl* deactivation in quenched and non-quenched LHCII preparations, referred to as Q-F730 and U-F680, respectively. It is found that the photoproduction of carotenoid (Car) triplet excitation in Q-F730 is substantially lower than that in U-F680, implying that intersystem crossing is unlikely to be the major deactivation channel of 1Chl*. In addition to the Chl-to-Car singlet excitation transfer pathway, our data are consistent with 1Chl deactivation via the formation of a Chl excimer and subsequent population of a Chl charge transfer state. Our spectroscopic results provide direct evidence linking the excimer to the Chl singlet excitation in LHCII, shedding light on the mechanistic basis of NPQ.

Article Details

Volume / Issue Vol. 163, Issue 19
Published November 21, 2025
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (9)

J

Jian-Wei Zou

College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,

D

Dan-Hong Li

College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,

R

Rong-Yao Gao

Key Laboratory of Advanced Light Conversion Materials and Biophotonics, Department of Chemistry and Life Resources, Renmin University of China 3 , Beijing 100872,

Y

Yu-Qian Li

Key Laboratory of Advanced Light Conversion Materials and Biophotonics, Department of Chemistry and Life Resources, Renmin University of China 3 , Beijing 100872,

Q

Qi-Rui Yu

College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,

Z

Zhi-Hao Yu

College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,

A

Alexander V. Ruban

Department of Biochemistry, School of Biological and Behavioural Sciences, Queen Mary University of London 2 , London E1 4NS,

J

Jian-Ping Zhang

J

Junrong Zheng

College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University 1 , Beijing 100871,