Detection of a multi-disease biomarker in saliva with graphene field effect transistors

Narendra Kumar, Mason Gray, Juan C. Ortiz-Marquez, Andrew Weber, Cameron R. Desmond, Avni Argun, Tim van Opijnen, Kenneth S. Burch
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Abstract

Human carbonic anhydrase 1 (CA1) has been suggested as a biomarker for identification of several diseases including cancers, pancreatitis, diabetes and Sjogren's syndrome. However, the lack of a rapid, cheap, accurate and easy-to-use quantification technique has prevented widespread utilization of CA1 for practical clinical applications. To this end, we present a label-free electronic biosensor for detection of CA1 utilizing highly sensitive graphene field effect transistors (G-FETs) as a transducer and specific RNA aptamers as a probe. The binding of CA1 with aptamers resulted in a positive shift in Dirac voltage VD of the G-FETs, the magnitude of which depended on target concentration. These aptameric G-FET biosensors showed the binding affinity (KD) of ~2.3 ng/ml (70 pM), which is four orders lower than that reported using a gel shift assay. This lower value of KD enabled us to achieve a detection range (10 pg/ml –100 ng/ml) which is well in line with the clinically relevant range. These highly sensitive devices allowed us to further prove their clinical relevance by successfully detecting the presence of CA1 in human saliva samples. Utilization of this label-free biosensor could facilitate the early-stage identification of various diseases associated with changes in concentration of CAs.

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用石墨烯场效应晶体管检测唾液中的多种疾病生物标志物
人类碳酸酐酶1 (CA1)已被认为是识别多种疾病的生物标志物,包括癌症、胰腺炎、糖尿病和干燥综合征。然而,缺乏一种快速、廉价、准确和易于使用的定量技术阻碍了CA1在实际临床应用中的广泛应用。为此,我们提出了一种用于检测CA1的无标签电子生物传感器,利用高灵敏度的石墨烯场效应晶体管(g - fet)作为换能器和特异性RNA适体作为探针。CA1与适配体的结合导致g - fet的Dirac电压VD的正位移,其幅度取决于靶浓度。这些适体G-FET生物传感器的结合亲和力(KD)为~2.3 ng/ml (70 pM),比凝胶移位法低4个数量级。这个较低的KD值使我们能够达到与临床相关范围非常一致的检测范围(10 pg/ml -100 ng/ml)。这些高度敏感的设备使我们能够通过成功检测人类唾液样本中CA1的存在进一步证明其临床相关性。利用这种无标记的生物传感器可以早期识别与CAs浓度变化相关的各种疾病。
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