A method for the selective isolation of multiply-charged peptides applicable in the quantitative proteomics
    55.
    发明公开
    A method for the selective isolation of multiply-charged peptides applicable in the quantitative proteomics 审中-公开
    过程用于定量蛋白质组学适用多电荷肽的选择性分离

    公开(公告)号:EP1785729A2

    公开(公告)日:2007-05-16

    申请号:EP06076889.2

    申请日:2006-10-16

    IPC分类号: G01N33/68

    摘要: The present invention describes a method that combines the blocking of primary amino groups and the cation exchange chromatography, to simplify peptide mixtures that can be generated or not by proteolytic or chemical treatments. This method allows the selective isolation of an average of 4 multiply-charged peptides (RH peptides) per protein and the study of 90% of the proteins of the analyzed proteomes. It is applicable to studies of quantitative proteomics without the usage of two-dimensional electrophorsis, it is compatible with any type of isotopic labeling and it is very useful to determine the differential expression of proteins present in multiple conditions (3 to 6 conditions) when using different isotopic labeling in a single experiment. The chromatographic system used also allows the fractionation fraction of the RH peptides to achieve the identification of a greater number of proteins.

    摘要翻译: 本发明描述了做了方法结合伯氨基和阳离子交换层析的阻塞,为了简化肽混合物也可以通过蛋白水解或化学处理来产生与否。 此方法允许将平均每蛋白4多电荷肽(RH肽)和所分析的蛋白质组中的蛋白质的90%的研究的选择性分离。 它适用于无二维electrophorsis的使用定量蛋白质组学研究中,它是与任何类型的同位素标记的兼容,它是非常有用的确定性矿存在于多个条件(3至6个条件)的蛋白质的差异表达当使用 不同同位素标记在单次实验。 使用这样的色谱系统允许RH肽的分馏部分,以实现蛋白的更大数量的识别。

    FO66 transgenic mice that express pathogenic mutants of the sca2 gene
    56.
    发明公开
    FO66 transgenic mice that express pathogenic mutants of the sca2 gene 审中-公开
    FO66转基因Mäuse,死亡病原菌Mutante des sca2 Gens exprimieren

    公开(公告)号:EP1704778A1

    公开(公告)日:2006-09-27

    申请号:EP05077830.7

    申请日:2005-12-09

    摘要: The present invention is related with the neurobiology and the transgenic animals, more specifically with obtaining a model to study the SCA2 genetic disease. The genome of one mice line has been modified through the introduction of a DNA segment that contains the necessary information for the synthesis of the human ataxin 2. In particular the invention is related with the transgenic mice F066 and the cellular lines able to express the human sca2 gene under the regulation of its self promoter. The F066 transgenic mice reproduce the features of the disease.
    The homozygous transgenic mouse line for the new gene was obtained through matting. This transgenic line is useful to study the mechanism that produce the disease and also will permit to prove new therapeutics that contributes to minimize the clinical symptoms in the patients.

    摘要翻译: 本发明涉及神经生物学和转基因动物,更具体地涉及获得研究SCA2遗传病的模型。 一条小鼠系的基因组已通过引入含有合成人ataxin2的必需信息的DNA片段进行修饰。特别地,本发明涉及转基因小鼠F066和能够表达人类的细胞系 sca2基因在其自身启动子的调节下。 F066转基因小鼠复制该疾病的特征。 通过消光获得新基因的纯合转基因小鼠品系。 该转基因系可用于研究产生该疾病的机制,并且还将允许证明有助于最小化患者临床症状的新治疗剂。

    ARTIFICIAL PROMOTER FOR THE EXPRESSION OF DNA SEQUENCES IN VEGETAL CELLS
    58.
    发明公开
    ARTIFICIAL PROMOTER FOR THE EXPRESSION OF DNA SEQUENCES IN VEGETAL CELLS 审中-公开
    人造的启动为DNA序列,植物细胞中表达

    公开(公告)号:EP1577395A1

    公开(公告)日:2005-09-21

    申请号:EP03767379.5

    申请日:2003-12-19

    IPC分类号: C12N15/82

    CPC分类号: C12N15/8216

    摘要: An artificial promoter characterized for been a chimerical recombinant DNA molecule such that, when introduced in any class of plant cells, promotes high expression levels of any DNA molecule fused to its 3' end. The basic genetic elements of the molecule described here are: a core promoter with a consensus TATA box, followed by an Exon/Intron/Exon region and a translation enhancer element, all of them artificially constructed. Transcription regulatory elements can be inserted upstream of the promoter here described to confer temporal-, organ- or tissue-specificity to the expression. The designed artificial genetic elements can be functionally inserted between any promoter active in plant cells and any DNA sequence to increase its transcription/translation levels.

    VECTOR FOR THE PRODUCTION OF TRANSPLASTOMIC ANGIOSPERM PLANTS
    59.
    发明公开
    VECTOR FOR THE PRODUCTION OF TRANSPLASTOMIC ANGIOSPERM PLANTS 审中-公开
    用于生产转移性血管内皮生长因子的载体

    公开(公告)号:EP1557468A2

    公开(公告)日:2005-07-27

    申请号:EP03798037.2

    申请日:2003-09-15

    IPC分类号: C12N15/82 A01H1/00 A01H5/00

    CPC分类号: C12N15/8214

    摘要: A DNA vector is provided for stable insertion and expression of heterologous genes in the plastid genomes of any Angiosperm plant cell. In this vector, foreign genes can be inserted in multiple cloning sites located at an artificial intergenic region obtained from the combination of atpB and rbcL operons that belong to plants of different Classes (dicotyledonous and monocotyledonous). The expression cassette is inserted into the plastid genome by homologous recombination between the atpB and rbcL border sequences of the vector with the corresponding homologous regions of plastid genome; in such a way that more than one gene of interest can be expressed under the transcriptional control of the rbcL promoter adjacent to the border region that encodes for the atpB gene.

    摘要翻译: 提供DNA载体用于在任何被子植物细胞的质体基因组中稳定插入和表达异源基因。 在该载体中,外源基因可以插入位于人工基因间区域的多个克隆位点,所述人工基因间区域来自属于不同类别(双子叶植物和单子叶植物)的植物的atpB和rbcL操纵子的组合。 表达盒通过载体的atpB和rbcL边界序列与质体基因组的相应同源区域之间的同源重组插入到质体基因组中; 使得可以在与编码atpB基因的边界区相邻的rbcL启动子的转录控制下表达多于一个的感兴趣基因。

    DNA fragments of the methylotrophic pichia pastoris yeast ICL gene
    60.
    发明公开
    DNA fragments of the methylotrophic pichia pastoris yeast ICL gene 审中-公开
    Methylotrophe Pichia pastoris Hefe ICL Gen DNA-Fragmente

    公开(公告)号:EP1162266A3

    公开(公告)日:2004-01-07

    申请号:EP01202009.5

    申请日:2001-05-28

    IPC分类号: C12N15/31 C12N15/81 C07K14/39

    CPC分类号: C07K14/39 C12N15/815

    摘要: This invention relates to the field of recombinant DNA technology. The present invention relates to the isolation of a DNA regulatory region, able to lead the expression of heterologous proteins in Pichia pastoris . In one of its aspects the invention is related to the isolation of a DNA fragment that contains the isocitrate lyase encoding gene (referred here as ICL ) from the yeast Pichia pastoris . In another aspects, this invention describes the use of a fragment derived from the described gene, which lead the expression of a foreign gene, when both are incorporated in a DNA vector and introduced in the host yeast Pichia pastoris. In this way the protein of interest is efficiently produced using this DNA fragment. In the yeast Pichia pastoris the expression of this gene is regulated in response to environmental conditions, such as the growth medium composition. The ICL expression is repressed when a carbon source like glucose is used, and induced when the carbon source present in the medium is ethanol or when the glucose is absent. An additional aspect, we have also isolated a DNA fragment consisting essentially of the Pichia pastoris ICL 3' transcription termination sequence.