Department of Chemistry, University of Connecticut, Storrs, CT 06269-3060, USA.
Instituto de Ciencia y Tecnología de Alimentos Córdoba (ICYTAC-CONICET), Ciudad Universitaria, Córdoba X5000HUA, Argentina.
Molecules. 2021 Apr 22;26(9):2441. doi: 10.3390/molecules26092441.
The increased interest in sequencing cyanobacterial genomes has allowed the identification of new homologs to both the N-terminal domain (NTD) and C-terminal domain (CTD) of the Orange Carotenoid Protein (OCP). The N-terminal domain homologs are known as Helical Carotenoid Proteins (HCPs). Although some of these paralogs have been reported to act as singlet oxygen quenchers, their distinct functional roles remain unclear. One of these paralogs (HCP2) exclusively binds canthaxanthin (CAN) and its crystal structure has been recently characterized. Its absorption spectrum is significantly red-shifted, in comparison to the protein in solution, due to a dimerization where the two carotenoids are closely placed, favoring an electronic coupling interaction. Both the crystal and solution spectra are red-shifted by more than 50 nm when compared to canthaxanthin in solution. Using molecular dynamics (MD) and quantum mechanical/molecular mechanical (QM/MM) studies of HCP2, we aim to simulate these shifts as well as obtain insight into the environmental and coupling effects of carotenoid-protein interactions.
对蓝藻基因组进行测序的兴趣日益浓厚,这使得人们能够鉴定出与橙色类胡萝卜素蛋白(OCP)的 N 端结构域(NTD)和 C 端结构域(CTD)都具有同源性的新基因。N 端结构域的同源物被称为螺旋类胡萝卜素蛋白(HCP)。尽管已经报道其中一些旁系同源物可以作为单线态氧猝灭剂,但它们的具体功能作用仍不清楚。其中一个旁系同源物(HCP2)专门结合角黄素(CAN),其晶体结构最近已被表征。由于两个类胡萝卜素紧密排列形成二聚体,导致其吸收光谱与溶液中的蛋白质相比发生明显红移,从而促进了电子耦合相互作用。与溶液中的角黄素相比,晶体和溶液光谱都发生了超过 50nm 的红移。通过对 HCP2 进行分子动力学(MD)和量子力学/分子力学(QM/MM)研究,我们旨在模拟这些位移,并深入了解类胡萝卜素-蛋白质相互作用的环境和耦合效应。