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Econo-Column® Chromatography Columns, 1.0 × 30 cm

公司名称: Bio-Rad Laboratories
产品编号: 7371032
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In vitro Assays for Eukaryotic Leading/Lagging Strand DNA Replication
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Date:
2017-09-20
[Abstract]  The eukaryotic replisome is a multiprotein complex that duplicates DNA. The replisome is sculpted to couple continuous leading strand synthesis with discontinuous lagging strand synthesis, primarily carried out by DNA polymerases ε and δ, respectively, along with helicases, polymerase α-primase, DNA sliding clamps, clamp loaders and many other proteins. We have previously established the mechanisms by which the polymerases ε and δ are targeted to their ‘correct’ strands, as well as quality control mechanisms that evict polymerases when they associate with an ‘incorrect’ strand. Here, we ... [摘要]  真核生物复制品是重复DNA的多蛋白复合物。 复制品被雕刻成连续的前导链合成与不连续的滞后链合成,主要通过DNA聚合酶ε和δ以及解旋酶,聚合酶α-引发酶,DNA滑动夹,夹带载体和许多其它蛋白质进行。 我们以前已经建立了聚合酶ε和δ靶向其“正确”链的机制,以及在与“不正确”链相关联时驱赶聚合酶的质量控制机制。 在这里,我们提供了使用纯蛋白质在体外差异测定前导和滞后链复制的实用指南。
Using pure proteins from Saccharomyces cerevisiae, our lab was the first to reconstitute a functional eukaryotic DNA replisome, a ~2 MDa complex that includes the 11-subunit CMG helicase (complex of Cdc45, Mcm2-7, GINS heterotetramer), the 4-subunit DNA polymerase (Pol) ε, the 4-subunit Pol α-primase, the PCNA (Proliferating Cell Nuclear Antigen) clamp homotrimer ring shaped processivity factor that ...

Liposome Disruption Assay to Examine Lytic Properties of Biomolecules
Author:
Date:
2017-08-05
[Abstract]  Proteins may have three dimensional structural or amino acid features that suggest a role in targeting and disrupting lipids within cell membranes. It is often necessary to experimentally investigate if these proteins and biomolecules are able to disrupt membranes in order to conclusively characterize the function of these biomolecules. Here, we describe an in vitro assay to evaluate the membrane lytic properties of proteins and biomolecules. Large unilamellar vesicles (liposomes) containing carboxyfluorescein at fluorescence-quenching concentrations are treated with the biomolecule ... [摘要]  蛋白质可以具有三维结构或氨基酸特征,其表明在细胞膜内靶向和破坏脂质的作用。通常有必要进行实验研究,如果这些蛋白质和生物分子能够破坏膜,以确定性地表征这些生物分子的功能。在这里,我们描述了一种体外实验来评估蛋白质和生物分子的膜裂解性质。用荧光猝灭浓度含有羧基荧光素的大单层囊泡(脂质体)用感兴趣的生物分子进行处理。由于染料从脂质体泄漏而导致的荧光增加,随后在缓冲液中的稀释表明生物分子足以破坏脂质体和膜。另外,由于脂质体破裂可能通过孔形成或通过类似于洗涤剂的脂类的一般溶解而发生,因此我们提供了区分这两种机制的方法。可以通过检查与适合孔的葡聚糖分子的羧基荧光素释放的封锁来鉴定和评估孔形成。这里描述的方法用于确定疟疾疫苗候选人CelTOS和促凋亡Bax通过孔形成破坏脂质体(Saito等人,2000; Jimah等人,2016) )。由于生物分子的膜脂质结合先于膜破裂,我们推荐使用伴侣方案:Jimah等人,2017。
【背景】该方案提出了评估蛋白质和其他生物分子的膜裂解性质的程序。该方案旨在清楚地描述研究生物分子的膜破坏性质所需的各种实验步骤。最后,该方案描述了膜破坏的定量测量,可用于提供对脂质体破坏的动力学和机制的了解。该方案成功地用于研究疟疾疫苗候选人CelTOS,其提供了对CelTOS的第一次体外功能测定的清楚描述。该方案的应用揭示,对于不饱和脂肪酸和多孔元素的CelTOS(透明性蛋白质)破坏了含有磷脂酸的膜。这一见解表明,CelTOS由入侵宿主细胞内的疟疾寄生虫分泌,以破坏宿主细胞膜并使寄生虫出现(Jimah等人,2016)。最后,该测定可以容易地应用于研究小分子,抗体或肽对CelTOS介导的脂质体破坏的抑制。当为CelTOS设计时,该协议易于泛化,适用于任何其他感兴趣的生物分子。 ...

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