Biogenic Amine Transporters: Mechanisms of Ligand Interaction.

描述(申请人提供)：多巴胺转运体(DAT)清除细胞外多巴胺，从而限制其释放后的寿命。清除过程包括DAT将多巴胺从外部转移到多巴胺能神经元内部。DAT是精神刺激药物的靶标，这些药物如DA，是被DAT(苯丙胺)摄取的底物，或者是抑制底物转位的阻滞剂(可卡因)。其他生物胺转运体是5-羟色胺转运体(SERT)和去甲肾上腺素转运体(NET)，这是许多不同抗抑郁药物的靶标。对这些蛋白质的结构洞察最近来自于细菌同源物亮氨酸转运体Leut的结晶，显示了底物结合位置(以下称为S1)，这是DAT、SERT和NET之间高度相似的区域。新的证据表明，在Leut的外前庭中存在一个次级底物位点(S2)，在底物摄取中起着重要作用。在反向摄取(外排)中，一个人可以假设S3位置在内前庭，与S2对称摄取。尚不清楚DAT、SERT或NET中是否存在S2或S3站点。我们将在结合(解离)实验以及摄取和外排试验中研究这些位点。将评估通过突变关键残基扰乱S2或S3位点的影响。Leut在初步实验中显示出DAT样的性质，它将与携带两个DA“头”的二价配体共结晶，使它们能够桥接S1和S2位点。此外，Leut将与二价亮氨酸共结晶，化合物也将被设计用于连接S1和S3。二价配体的结合，如果需要对Leut进行额外的修饰，可能会促进Leut的内向状态，到目前为止，对其结构的阐明一直难以捉摸。据我们所知，目前还没有观察到以S2为衬底的Leut晶体。虽然大量的证据表明DAT和其他生物胺转运体的寡聚体组装，但它们的功能作用尚不清楚。我们将检验寡聚DAT组装中的单个原型不独立发挥作用的假设，并建立积极或消极的合作相互作用。有证据表明生物胺转运蛋白的寡聚化和糖基化密切相关，但有相反的证据表明，在转运蛋白从细胞核到内质网再到高尔基体再到表面的成熟过程中，哪一个最先成熟。我们将研究寡聚、糖基化和DAT转运之间的关系。工具将是产生部分糖基化转运蛋白的Lec 4细胞，这种结构缺乏三个N连接的糖基化位点，以及一系列具有编码变异的DAT突变，我们已经证明在人类中与多巴胺转运蛋白缺乏综合征(DTDS)有关，DTDS是一种遗传性早发性婴儿帕金森氏症-肌张力障碍。该项目的长期目标是更好地了解生物胺转运体的结构和功能，这对靶向DAT、SERT和NET的化合物的作用非常重要：滥用药物、治疗注意力缺陷多动障碍的药物、环境毒素和抗抑郁药物。

DESCRIPTION (provided by applicant): The dopamine transporter (DAT) clears extracellular dopamine thereby limiting its lifetime after release. The clearance process consists of DAT translocating dopamine from the outside to the inside of dopaminergic neurons. The DAT is a target for psychostimulant drugs which, as DA, are substrates taken up by DAT (amphetamine), or are blockers inhibiting substrate translocation (cocaine). Other biogenic amine transporters are the serotonin transporter (SERT) and the norepinephrine transporter (NET), targets for many different antidepressant drugs. Structural insight into these proteins has recently come from crystallization of a bacterial homolog, the leucine transporter LeuT, showing the location of the substrate binding site (termed S1 in the following), a region with high similarity among DAT, SERT, and NET. Novel evidence indicates the presence in LeuT of a secondary substrate site (S2) in the outer vestibule, playing a fundamental role in substrate uptake. In reversed uptake (efflux), one can postulate an S3 site in the inner vestibule, in symmetry to S2 in uptake. It is nt known whether S2 or S3 sites exist in DAT, SERT, or NET. We will study these sites in binding (dissociation) experiments, and in uptake and efflux assays. The impact will be assessed of disrupting S2 or S3 sites by mutating key residues. LeuT, which in preliminary experiments shows DAT-like properties, will be co-crystallized with bivalent ligands carrying two DA "heads" enabling them to bridge S1 and S2 sites. In addition, LeuT will be co-crystallized with bivalent leucine, and compounds will also be designed for bridging S1 and S3. Binding of bivalent ligands, if needed with additional modifications of LeuT, may promote an inward-facing state of leuT, the structural elucidation of which has been elusive so far. No LeuT crystals with substrate in S2 have yet been visualized to our knowledge. Although abundant evidence points to oligomeric assemblies of DAT and other biogenic amine transporters, their functional role is not clear. We will test the hypothesis that individual protomers in an oligomeric DAT assembly are not functioning independently, and establish positive or negative cooperative interactions. There is evidence that oligomerization and glycosylation of biogenic amine transporters are intimately linked, but there is contrasting evidence as to which comes first in maturation of the transporter as it moves from nucleus to endoplasmic reticulum to Golgi to surface. We will study the relationship between oligomerization, glycosylation, and trafficking of DAT. Tools will be Lec 4 cells that produce partially glycosylated transporter, a construct that lacks the three N-linked glycosylation sites, and an assortment of DAT mutants with coding variations in humans we have shown to be linked with Dopamine Transporter Deficiency Syndrome (DTDS), an inherited early-onset infantile parkinsonism-dystonia. The long-term objectives of the project are to better understand biogenic amine transporter structure-function, important for the action of compounds that target DAT, SERT, and NET: drugs of abuse, medications for attention-deficit hyperactivity disorder, environmental toxins, and antidepressants.