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Integrated microfluidic and imaging platform for a kinase activity radioassay to analyze minute patient cancer samples

机译:集成的微流控和成像平台用于激酶活性放射分析,可分析微小的患者癌症样品

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摘要

Oncogenic kinase activity and the resulting aberrant growth and survival signaling are a common driving force of cancer. Accordingly, many successful molecularly targeted anticancer therapeutics are directed at inhibiting kinase activity. To assess kinase activity in minute patient samples, we have developed an immunocapture-based in vitro kinase assay on an integrated polydimethylsiloxane microfluidics platform that can reproducibly measure kinase activity from as few as 3,000 cells. For this platform, we adopted the standard radiometric 32P-ATP-labeled phosphate transfer assay. Implementation on a microfluidic device required us to develop methods for repeated trapping and mixing of solid-phase affinity microbeads. We also developed a solid-state beta-particle camera imbedded directly below the microfluidic device for real-time quantitative detection of the signal from this and other microfluidic radiobioassays. We show that the resulting integrated device can measure ABL kinase activity from BCR-ABL-positive leukemia patient samples. The low sample input requirement of the device creates new potential for direct kinase activity experimentation and diagnostics on patient blood, bone marrow, and needle biopsy samples.
机译:致癌激酶活性以及由此产生的异常生长和生存信号是癌症的常见驱动力。因此,许多成功的分子靶向抗癌治疗剂针对抑制激酶活性。为了评估微小患者样品中的激酶活性,我们在集成的聚二甲基硅氧烷微流体平台上开发了一种基于免疫捕获的体外激酶测定方法,该平台可重现性地测量多达3,000个细胞的激酶活性。在该平台上,我们采用了标准的放射性32P-ATP标记的磷酸盐转移测定法。在微流体装置上的实现要求我们开发用于重复捕集和混合固相亲和力微珠的方法。我们还开发了直接位于微流控设备下方的固态β粒子照相机,用于实时定量检测此方法和其他微流控放射生物测定法的信号。我们表明,最终的集成设备可以从BCR-ABL阳性白血病患者样本中测量ABL激酶活性。该设备的低样品输入要求为直接对患者血液,骨髓和穿刺活检样品进行激酶活性实验和诊断创造了新的潜力。

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