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Structures of bacterial homologues of SWEET transporters in two distinct conformations

机译:两种不同构型的SWEET转运蛋白细菌同源物的结构

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摘要

SWEETs and their prokaryotic homologues are monosaccharide and disaccharide transporters that are present from Archaea to plants and humans. SWEETs play crucial roles in cellular sugar efflux processes: that is, in phloem loading, pollen nutrition and nectar secretion. Their bacterial homologues, which are called SemiSWEETs, are among the smallest known transporters. Here we show that SemiSWEET molecules, which consist of a triple-helix bundle, form symmetrical, parallel dimers, thereby generating the translocation pathway. Two SemiSWEET isoforms were crystallized, one in an apparently open state and one in an occluded state, indicating that SemiSWEETs and SWEETs are transporters that undergo rocking-type movements during the transport cycle. The topology of the triple-helix bundle is similar yet distinct to that of the basic building block of animal and plant major facilitator superfamily (MFS) transporters (for example, GLUTs and SUTs). This finding indicates two possibilities: that SWEETs and MFS transporters evolved from an ancestral triple-helix bundle or that the triple-helix bundle represents convergent evolution. In SemiSWEETs and SWEETs, two triple-helix bundles are arranged in a parallel configuration to produce the 6- and 6 + 1-transmembrane-helix pores, respectively. In the 12-transmembrane-helix MFS transporters, four triple-helix bundles are arranged into an alternating antiparallel configuration, resulting in a much larger 2×2 triple-helix bundle forming the pore. Given the similarity of SemiSWEETs and SWEETs to PQ-loop amino acid transporters and to mitochondrial pyruvate carriers (MPCs), the structures characterized here may also be relevant to other transporters in the MtN3 clan. The insight gained from the structures of these transporters and from the analysis of mutations of conserved residues will improve the understanding of the transport mechanism, as well as allow comparative studies of the different superfamilies involved in sugar transport and the evolution of transporters in general.
机译:SWEET及其原核同源物是从古细菌到植物和人类的单糖和二糖转运蛋白。 SWEET在细胞糖流出过程中起着至关重要的作用:即在韧皮部负载,花粉营养和花蜜分泌中。它们的细菌同源物称为SemiSWEET,是已知的最小转运蛋白。在这里,我们显示由三重螺旋束组成的SemiSWEET分子形成对称的平行二聚体,从而产生易位途径。两种SemiSWEET亚型均已结晶,一种处于明显开放状态,一种处于闭塞状态,这表明SemiSWEET和SWEET是在运输周期中经历摇摆型运动的转运蛋白。三螺旋束的拓扑与动植物主要易化子超家族(MFS)转运蛋白(例如,GLUT和SUT)的基本构建基块的拓扑结构相似但又截然不同。这一发现表明了两种可能性:SWEET和MFS转运蛋白从祖先的三螺旋束演化而来,或者说三螺旋束代表融合演化。在SemiSWEET和SWEET中,两个三螺旋束以平行配置排列,分别产生6和6 + 1跨膜螺旋孔。在12个跨膜螺旋MFS转运蛋白中,四个三螺旋束排列成交替的反平行构型,导致形成孔的更大的2×2三螺旋束。鉴于SemiSWEET和SWEET与PQ环氨基酸转运蛋白和线粒体丙酮酸载体(MPC)相似,此处表征的结构也可能与MtN3家族中的其他转运蛋白有关。从这些转运蛋白的结构和保守残基突变的分析中获得的见识将增进对转运机理的理解,并允许对糖转运中涉及的不同超家族以及转运蛋白的总体进化进行比较研究。

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  • 来源
    《Nature》 |2014年第7527期|448-452|共5页
  • 作者单位

    Department of Molecular and Cellular Physiology, 279 Campus Drive, Stanford University School of Medicine, Stanford, California 94305, USA;

    Department of Molecular and Cellular Physiology, 279 Campus Drive, Stanford University School of Medicine, Stanford, California 94305, USA;

    Department of Plant Biology, Carnegie Institution for Science, 260 Panama Street, Stanford, California 94305, USA;

    Department of Molecular and Cellular Physiology, 279 Campus Drive, Stanford University School of Medicine, Stanford, California 94305, USA;

    Department of Plant Biology, Carnegie Institution for Science, 260 Panama Street, Stanford, California 94305, USA;

    Department of Biology, Stanford University, Stanford, California 94305, USA;

    NE-CAT and Department of Chemistry and Chemical Biology, Cornell University, Building 436E, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60439, USA;

    Department of Plant Biology, Carnegie Institution for Science, 260 Panama Street, Stanford, California 94305, USA,Department of Biology, Stanford University, Stanford, California 94305, USA;

    Department of Molecular and Cellular Physiology, 279 Campus Drive, Stanford University School of Medicine, Stanford, California 94305, USA;

  • 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 02:53:16

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