Absolute Quantification of Nav1.5 Expression by Targeted Mass Spectrometry.
Sarah L AdamsGe ChangMohamed A FoudaSharwan KumarBingyun SunPublished in: International journal of molecular sciences (2022)
Nav1.5 is the pore forming α-subunit of the cardiac voltage-gated sodium channel that initiates cardiac action potential and regulates the human heartbeat. A normal level of Nav1.5 is crucial to cardiac function and health. Over- or under-expression of Nav1.5 can cause various cardiac diseases ranging from short PR intervals to Brugada syndromes. An assay that can directly quantify the protein amount in biological samples would be a priori to accurately diagnose and treat Nav1.5-associated cardiac diseases. Due to its large size (>200 KD), multipass transmembrane domains (24 transmembrane passes), and heavy modifications, Nav1.5 poses special quantitation challenges. To date, only the relative quantities of this protein have been measured in biological samples. Here, we describe the first targeted and mass spectrometry (MS)-based quantitative assay that can provide the copy numbers of Nav1.5 in cells with a well-defined lower limit of quantification (LLOQ) and precision. Applying the developed assay, we successfully quantified transiently expressed Nav1.5 in as few as 1.5 million Chinese hamster ovary (CHO) cells. The obtained quantity was 3 ± 2 fmol on the column and 3 ± 2 × 10 4 copies/cell. To our knowledge, this is the first absolute quantity of Nav1.5 measured in a biological sample.
Keyphrases
- mass spectrometry
- liquid chromatography
- left ventricular
- healthcare
- induced apoptosis
- poor prognosis
- high throughput
- public health
- high resolution
- endothelial cells
- binding protein
- cell cycle arrest
- high performance liquid chromatography
- mental health
- ms ms
- cancer therapy
- heart failure
- stem cells
- risk assessment
- mesenchymal stem cells
- long non coding rna
- gas chromatography
- induced pluripotent stem cells
- human health