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A peptide array-based serological protein kinase A activity assay and its application in cancer diagnosis

机译:基于肽阵列的血清蛋白激酶A活性测定及其在癌症诊断中的应用

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摘要

Protein kinase A (PKA) plays a crucial role in several biological processes; however, there is no assay with sufficient sensitivity and specificity to determine serological PKA (sPKA) activity. Here we present an on-chip activity assay that employs cysteine-modified kemptide arrays to determine specific sPKA activity in human sera that eliminates the potential contributions of other kinases with a protein kinase peptide inhibitor. The sensitivity of the on-chip sPKA activity assay was greatly enhanced by Triton X-100, with a 0.01 U mL(-1) detection limit. sPKA activity was determined by subtracting nonspecific sPK activity from total sPK activity. Our assay provided greater sensitivity and specificity and more accurate area under the curve values for gastric cancer compared to the total sPK activity assay. sPKA activities in human sera from patients with hepatic (n = 30), gastric (n = 30), lung (n = 30), and colorectal (n = 30) cancers were significantly higher than those in controls (n = 30, p < 10(-4)), but no significant difference in sPKA activities between normal and inflammation groups was observed. These results demonstrate that the on-chip assay accurately measures sPKA activity in human sera and that the sPKA activity may be a potential biomarker for cancer diagnosis.
机译:蛋白激酶A(PKA)在几个生物学过程中起着至关重要的作用;但是,没有一种测定方法具有足够的灵敏度和特异性来确定血清学PKA(sPKA)活性。在这里,我们介绍了一种芯片上的活性测定法,该方法采用半胱氨酸修饰的kemptide阵列来确定人血清中的特定sPKA活性,从而消除了其他激酶与蛋白激酶肽抑制剂的潜在作用。 Triton X-100大大提高了芯片上sPKA活性测定的灵敏度,检测极限为0.01 U mL(-1)。 sPKA活性是通过从总sPK活性中减去非特异性sPK活性来确定的。与总sPK活性测定相比,我们的测定为胃癌提供了更高的敏感性和特异性,并且曲线值下的面积更准确。肝癌(n = 30),胃癌(n = 30),肺癌(n = 30)和结直肠癌(n = 30)患者的人血清中sPKA活性显着高于对照组(n = 30,p <10(-4)),但在正常组和炎症组之间未观察到sPKA活性的显着差异。这些结果表明,片上测定法可以准确地测量人血清中的sPKA活性,并且sPKA活性可能是癌症诊断的潜在生物标记。

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