Fast Label-Free Metabolic Profile Recognition Identifies Phenylketonuria and Subtypes

Phenylketonuria (PKU) is the most common inherited metabolic disease in humans. Clinical screening of newborn heel blood samples for PKU is costly and time-consuming because it requires multiple procedures, like isotope labeling and derivatization, and PKU subtype identification requires an additional urine sample. Delayed diagnosis of PKU, or subtype identification can result in mental disability. Here, plasmonic silver nanoshells are used for laser desorption/ionization mass spectrometry (MS) detection of PKU with label-free assay by recognizing metabolic profile in dried blood spot (DBS) samples. A total of 1100 subjects are recruited and each DBS sample can be processed in seconds. This platform achieves PKU screening with a sensitivity of 0.985 and specificity of 0.995, which is comparable to existing clinical liquid chromatography MS (LC-MS) methods. This method can process 360 samples per hour, compared with the LC-MS method which processes only 30 samples per hour. Moreover, this assay enables precise identification of PKU subtypes without the need for a urine sample. It is demonstrated that this platform enables high-performance and fast, low-cost PKU screening and subtype identification. This approach might be suitable for the detection of other clinically relevant biomarkers in blood or other clinical samples. The plasmonic silver nanoshells constructed microarrays are used for laser desorption/ionization mass spectrometry (MS) detection of phenylketonuria (PKU) by recognizing metabolic profile in dried blood spot (DBS) samples. The platform achieves precise PKU diagnosis and subtype identification in a single DBS test with a fast, label-free, and low-cost assay, comparable to existing clinical liquid chromatography MS methods. image