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    • 2. 发明申请
    • REAGENTS FOR THE DETECTION OF PROTEIN PHOSPHORYLATION IN SIGNALING PATHWAYS
    • 用于检测信号通路中的蛋白质磷酸化的试剂
    • WO2008008998A2
    • 2008-01-17
    • PCT/US2007/073534
    • 2007-07-13
    • CELL SIGNALING TECHNOLOGY, INC.HORNBECK, PeterGOSS, ValerieLEE, KimberlyGU, Ting-LeiMORITZ, Albrecht
    • HORNBECK, PeterGOSS, ValerieLEE, KimberlyGU, Ting-LeiMORITZ, Albrecht
    • G01N33/53
    • G01N33/68C07K16/18C07K16/32C07K16/40G01N33/60G01N33/6842G01N33/6845G01N33/6848
    • The invention discloses novel phosphorylation sites identified in signal transduction proteins and pathways, and provides phosphorylation-site specific antibodies and heavy-isotope labeled peptides (AQUA peptides) for the selective detection and quantification of these phosphorylated sites/proteins, as well as methods of using the reagents for such purpose. Among the phosphorylation sites identified are sites occurring in the following protein types: adaptor/scaffold proteins, adhesion/extracellular matrix protein, apoptosis proteins, calcium binding proteins, cell cycle regulation proteins, chaperone proteins, chromatin, DNA binding/repair/replication proteins, cytoskeletal proteins, endoplasmic reticulum or golgi proteins, enzyme proteins, G/regulator proteins, inhibitor proteins, motor/contractile proteins, phosphatase, protease, Ser/ Thr protein kinases, protein kinase (Tyr)s, receptor/channel/cell suface proteins, RNA binding proteins, transcriptional regulators, tumor suppressor proteins, ubiquitan conjugating system proteins and proteins of unknown function.
    • 本发明公开了在信号转导蛋白质和途径中鉴定的新的磷酸化位点,并提供磷酸化位点特异性抗体和重同位素标记肽(AQUA肽)用于选择性检测和定量这些磷酸化位点/ 蛋白质以及为此目的使用试剂的方法。 在所鉴定的磷酸化位点中存在发生在以下蛋白质类型中的位点:衔接子/支架蛋白质,粘附/细胞外基质蛋白质,凋亡蛋白质,钙结合蛋白质,细胞周期调节蛋白质,分子伴侣蛋白质,染色质,DNA结合/修复/ 细胞骨架蛋白,内质网或高尔基蛋白,酶蛋白,G /调节蛋白,抑制蛋白,运动/收缩蛋白,磷酸酶,蛋白酶,Ser / Thr蛋白激酶,蛋白激酶(Tyr) RNA结合蛋白,转录调节因子,肿瘤抑制蛋白,泛素缀合系统蛋白和功能未知的蛋白。
    • 3. 发明申请
    • REAGENTS FOR THE DETECTION OF PROTEIN ACETYLATION SIGNALING PATHWAYS
    • 检测蛋白质乙酰化信号途径的试剂
    • WO2007133689A2
    • 2007-11-22
    • PCT/US2007/011420
    • 2007-05-11
    • CELL SIGNALING TECHNOLOGY, INC.GUO, AilanLI, YuGU, Ting-leiMITCHELL, JeffreyHORNBECK, Peter
    • GUO, AilanLI, YuGU, Ting-leiMITCHELL, JeffreyHORNBECK, Peter
    • B21D11/10
    • G01N33/6842C07K16/44
    • The invention discloses 426 novel acetylation sites identified in signal transduction proteins and pathways underlying human protein acetylation signaling pathways, and provides acetylation-site specific antibodies and heavy-isotope labeled peptides (AQUA peptides) for the selective detection and quantification of these acetylated sites/proteins, as well as methods of using the reagents for such purpose. Among the acetylation sites identified are sites occurring in the following protein types: Methyltransferases, Transcription factors, Transcription coactivators, Translation initiation complex proteins, Oxireductases, Protein kinases, RNA binding proteins, Secreted proteins, Transferases, Transporter proteins, Ubiquitin conjugating system proteins, Motor proteins, Phosphotases, Proteases, Phospholipases, Receptor proteins and Vesicle proteins.
    • 本发明公开了在信号转导蛋白中鉴定的426个新的乙酰化位点和人蛋白质乙酰化信号通路的途径,并提供乙酰化位点特异性抗体和重同位素标记肽(AQUA肽),用于选择性检测和定量这些乙酰化位点/蛋白质 ,以及使用试剂用于此目的的方法。 确定的乙酰化位点之间的位点是发生在以下蛋白质类型中的位点:甲基转移酶,转录因子,转录共激活因子,翻译起始复合蛋白​​,氧化还原酶,蛋白激酶,RNA结合蛋白,分泌蛋白,转移酶,转运蛋白,泛素缀合系统蛋白,马达 蛋白质,磷酸酶,蛋白酶,磷脂酶,受体蛋白和囊泡蛋白。
    • 5. 发明申请
    • TRANSLOCATION AND MUTANT TNK1 KINASE IN HUMAN LYMPHOMA
    • 跨淋巴细胞和突变型TNK1在人淋巴瘤中的激酶
    • WO2009075825A2
    • 2009-06-18
    • PCT/US2008/013516
    • 2008-12-08
    • CELL SIGNALING TECHNOLOGY, INC.GU, Ting-Lei
    • GU, Ting-Lei
    • C12N9/12
    • C12N9/12
    • In accordance with the invention, a novel gene translocation in human Hodgkin's lymphoma (HL) that results in a fusion protein combining part of C17ORF61 with Thirty-eight-negative kinase 1 (Tnkl) kinase has now been identified. The TNK1-C17ORF61 fusion protein, which retains TNKl tyrosine kinase activity, was confirmed to drive the proliferation and survival of Hodgkin's lymphoma (HL) cell line, L-540. The invention therefore provides, in part, isolated polynucleotides and vectors encoding the disclosed mutant TNKl kinase polypeptides, probes for detecting it, isolated mutant polypeptides, recombinant polypeptides, and reagents for detecting the fusion and truncated polypeptides. The disclosed identification of this new fusion protein and truncated kinase enables new methods for determining the presence of these mutant TNK1 kinase polypeptides in a biological sample, methods for screening for compounds that inhibit the proteins, and methods for inhibiting the progression of a cancer characterized by the mutant polynucleotides or polypeptides, which are also provided by the invention.
    • 根据本发明,人霍奇金淋巴瘤(HL)中的新基因易位导致融合蛋白结合部分C17ORF61与三十八阴性激酶1(Tnk1)激酶 鉴定。 保留TNK1酪氨酸激酶活性的TNK1-C17ORF61融合蛋白被证实能够驱动霍奇金淋巴瘤(HL)细胞系L-540的增殖和存活。 因此,本发明部分地提供了编码所公开的突变型TNK1激酶多肽的分离的多核苷酸和载体,用于检测它的探针,分离的突变多肽,重组多肽和用于检测融合和截短的多肽的试剂。 所公开的这种新的融合蛋白和截短的激酶的鉴定使得能够确定生物样品中这些突变型TNK1激酶多肽的存在的新方法,筛选抑制蛋白质的化合物的方法,以及抑制癌症进展的方法,其特征在于 突变的多核苷酸或多肽,其也由本发明提供。