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在超高磁场下通过固态核磁共振光谱对均匀[13C,15N]标记的光捕获复合物中B800和B850细菌叶绿素进行选择性化学位移归属。

Selective chemical shift assignment of B800 and B850 bacteriochlorophylls in uniformly [13C,15N]-labeled light-harvesting complexes by solid-state NMR spectroscopy at ultra-high magnetic field.

作者信息

van Gammeren Adriaan J, Buda Francesco, Hulsbergen Frans B, Kiihne Suzanne, Hollander Johan G, Egorova-Zachernyuk Tatjana A, Fraser Niall J, Cogdell Richard J, de Groot Huub J M

机构信息

Leiden Institute of Chemistry, Gorlaeus Laboratoria, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands.

出版信息

J Am Chem Soc. 2005 Mar 9;127(9):3213-9. doi: 10.1021/ja044215a.

Abstract

The electronic ground states of the bacteriochlorophyll a type B800 and type B850 in the light-harvesting 2 complex of Rhodopseudomonas acidophila strain 10050 have been characterized by magic angle spinning (MAS) dipolar (13)C-(13)C correlation NMR spectroscopy. Uniformly [(13)C,(15)N] enriched light-harvesting 2 (LH2) complexes were prepared biosynthetically, while [(13)C,(15)N]-B800 LH2 complexes were obtained after reconstitution of apoprotein with uniformly [(13)C,(15)N]-enriched bacteriochlorophyll cofactors. Extensive sets of isotropic (13)C NMR chemical shifts were obtained for each bacteriochlorin ring species in the LH2 protein. (13)C isotropic shifts in the protein have been compared to the corresponding shifts of monomeric BChl a dissolved in acetone-d(6). Density functional theory calculations were performed to estimate ring current effects induced by adjacent cofactors. By correction for the ring current shifts, the (13)C shift effects due to the interactions with the protein matrix were resolved. The chemical shift changes provide a clear evidence for a global electronic effect on the B800 and B850 macrocycles, which is attributed to the dielectrics of the protein environment, in contrast with local effects due to interaction with specific amino acid residues. Considerable shifts of -6.2 < Deltasigma < +5.8 ppm are detected for (13)C nuclei in both the B800 and the B850 bacteriochlorin rings. Because the shift effects for the B800 and B850 are similar, the polarization of the electronic ground states induced by the protein environment is comparable for both cofactors and corresponds with a red shift of approximately 30 nm relative to the monomeric BChl dissolved in acetone-d(6). The electronic coupling between the B850 cofactors due to macrocycle overlap is the predominant mechanism behind the additional red shift in the B850.

摘要

嗜酸性红假单胞菌10050菌株捕光2复合物中细菌叶绿素a的B800型和B850型的电子基态已通过魔角旋转(MAS)偶极(13)C - (13)C相关核磁共振光谱进行了表征。通过生物合成制备了均匀富集[(13)C,(15)N]的捕光2(LH2)复合物,而在用均匀富集[(13)C,(15)N]的细菌叶绿素辅因子重组载脂蛋白后获得了[(13)C,(15)N] - B800 LH2复合物。对于LH2蛋白中每个细菌叶绿素环物种,获得了大量的各向同性(13)C NMR化学位移。已将蛋白中的(13)C各向同性位移与溶解在氘代丙酮中的单体BChl a的相应位移进行了比较。进行了密度泛函理论计算以估计相邻辅因子引起的环电流效应。通过校正环电流位移,解析了与蛋白质基质相互作用引起的(13)C位移效应。化学位移变化为蛋白质环境对B800和B850大环的全局电子效应提供了明确证据,这归因于蛋白质环境的介电常数,与与特定氨基酸残基相互作用产生的局部效应形成对比。在B800和B850细菌叶绿素环中的(13)C核检测到相当大的位移 - 6.2 < Δσ < +5.8 ppm。由于B800和B850的位移效应相似,蛋白质环境诱导的电子基态极化对于两种辅因子是可比的,并且相对于溶解在氘代丙酮中的单体BChl对应于约30 nm的红移。B850辅因子之间由于大环重叠引起的电子耦合是B850中额外红移背后的主要机制。

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