Key result
A capillary electrophoresis-electrospray ionization mass spectrometry method successfully monitored the dynamic generation and breakdown of at least five BNP peptidoforms in human plasma.
A novel CESI-MS method allows for rapid profiling of BNP proteolysis in human plasma, offering potential applications in heart failure diagnostics and monitoring of therapeutic BNP infusion.
CESI-MS enables BNP peptidoform monitoring in plasma; leaves open its diagnostic role in heart failure pending validation.
B-type Natriuretic Peptide (BNP) is a biologically active circulating hormone. Plasma concentrations of BNP are routinely used in the diagnosis of heart failure, and the intravenous infusion of recombinant BNP can be used for heart failure treatment. Like many bioactive polypeptides, multiple plasma enzymes are known to cleave circulating BNP, and as part of the CVD-B/D-HPP mandate, we sought to develop a technique capable of profiling these catabolic processes in plasma. We used a neutral-coated capillary electrophoresis-electrospray ionization (CESI) separation system coupled with high-resolution mass spectrometry to profile the proteolysis of exogenous recombinant BNP 1–32 in plasma. Our method utilizes electrokinetic injection of minimally processed plasma samples to simultaneously monitor the dynamic generation and breakdown of at least five BNP peptidoforms in plasma. By integrating multisegment injection, our method can produce a multipoint BNP proteolytic profile for one sample within an hour. We envision applying this method to assess the potential relation between plasma-based BNP proteolysis and heart failure as well as a means of monitoring BNP bioavailability after therapeutic infusion.
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Zhang et al. (2017) studied Heart failure. Capillary electrophoresis-electrospray ionization (CESI) mass spectrometry was evaluated on Profiling the proteolysis of exogenous recombinant BNP 1-32 in plasma. A capillary electrophoresis-electrospray ionization mass spectrometry method successfully monitored the dynamic generation and breakdown of at least five BNP peptidoforms in human plasma.
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