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Zinc-Bacteriochlorophyllide Dimers in de Novo Designed Four-Helix Bundle Proteins. A Model System for Natural Light Energy Harvesting and Dissipation

机译:从头设计的锌-细菌叶绿素二聚体设计为四螺旋束蛋白质。自然光能量收集与耗散的模型系统

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摘要

Photosynthetic organisms utilize interacting pairs of chlorophylls and bacteriochlorophylls as excitation energy donors and acceptors in light harvesting complexes, as photosensitizers of charge separation in reaction centers, and maybe as photoprotective quenching centers that dissipate excess excitation energy under high light intensities. To better understand how the pigment's local environment and spatial organization within the protein tune its ground- and excited-state properties to perform different functions, we prepared and characterized the simplest possible system of interacting bacteriochlorophylls within a protein scaffold. Using HP7, a high-affinity heme-binding protein of the HP class of de novo designed four-helix bundles, we incorporated 13~2-OH-zinc-bacteriochlorophyllide-a (ZnBChlide), a water-soluble bacteriochlorophyll derivative, into specific binding sites within the four-helix bundle protein core. We capitalized on the rich and informative optical spectrum of ZnBChlide to rigorously characterize its complexes with HP7 and two variants, in which a single heme-binding site is eliminated by replacing histidine residues at positions 7 or 42 by phenylalanine. Surprisingly,we found the ZnBChlide binding capacity of HP7 and its variants to be higher than for heme: up to three ZnBChlide pigments bind per HP7, or two per each single histidine variant. The formation of dimers within HP7 results in dramatic quenching of ZnBChlide fluorescence, reducing its quantum yield by about 80%, and the singlet excited-state lifetime by 2 orders of magnitudes compared to the monomer. Thus, HP7 and its variants are the first examples of a simple protein environment that can isolate a self-quenching pair of photosynthetic pigments in pure form. Unlike its complicated natural analogues, this system can be constructed from the ground up, starting with the simplest functional element, increasing the complexity as needed.
机译:光合生物利用相互作用的叶绿素和细菌叶绿素对作为光收集复合体中的激发能供体和受体,用作反应中心电荷分离的光敏剂,并可能作为光保护性猝灭中心,在高光强度下消散多余的激发能。为了更好地了解蛋白质中色素的局部环境和空间组织如何调整其基态和激发态特性以执行不同的功能,我们准备并表征了蛋白质支架中最简单的相互作用细菌叶绿素系统。使用HP 7从头设计的HP类高亲和力血红素结合蛋白设计的四螺旋束,我们将13〜2-OH-锌细菌性叶绿素a(ZnBChlide)(一种水溶性细菌叶绿素衍生物)掺入了特定的四螺旋束蛋白核心内的结合位点。我们利用ZnBChlide丰富而有益的光谱来严格表征其与HP7和两个变体的配合物,其中单个血红素结合位点通过用苯丙氨酸替换7或42位的组氨酸残基而消除。出人意料的是,我们发现HP7及其变体的ZnBChlide结合能力比血红素高:每个HP7最多结合三个ZnBChlide颜料,每个单个组氨酸变体最多结合两个。与单体相比,HP7中二聚体的形成导致ZnBChlide荧光显着淬灭,其量子产率降低了约80%,单线态的激发态寿命降低了2个数量级。因此,HP7及其变体是简单蛋白质环境的第一个实例,可以隔离纯形式的自猝灭光合色素。与复杂的自然类似物不同,该系统可以从头开始构建,从最简单的功能元素开始,根据需要增加复杂性。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第24期|p.9526-9535|共10页
  • 作者单位

    Plant Sciences Department, Weizmann Institute of Science, Rehovot 76100, Israel;

    Max Planck Institute for Bioinorganic Chemistry, Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany Institut fur Physikalische and Theoretische Chemie, Rheinische Friedrich-Wilhelms Universitat Bonn, Bonn, Germany;

    Plant Sciences Department, Weizmann Institute of Science, Rehovot 76100, Israel Group of Biological Physics, Institute of Physics, Polish Academy of Science, Warsaw, Poland.,;

    Plant Sciences Department, Weizmann Institute of Science, Rehovot 76100, Israel;

    Plant Sciences Department, Weizmann Institute of Science, Rehovot 76100, Israel;

    Max Planck Institute for Bioinorganic Chemistry, Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany;

    Plant Sciences Department, Weizmann Institute of Science, Rehovot 76100, Israel;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:14:18

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