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Proteomics and Protein Markers |
Departments of1
Physiology and 2
Pharmacology and Toxicology, Biocenter Oulu, University of Oulu, Oulu, Finland.
3 Department of Internal Medicine, Kuopio University Hospital, Kuopio, Finland.
4 Department of Pediatrics, Helsinki University Hospital, Helsinki, Finland.
aAddress correspondence to this author at: Department of Physiology, Faculty of Medicine, PO Box 5000, University of Oulu, Oulu, FIN-90014 Finland. Fax 358-8-5375320; e-mail olli.vuolteenaho{at}oulu.fi.
Background: The N-terminal fragments of A- and B-type natriuretic peptides (NT-proANP and NT-proBNP) are powerful markers of cardiac function. The current assays require refinement with regard to standardization with native calibrators and the ability to detect the actual circulating forms.
Methods: The following peptides were prepared with recombinant methods: NT-proANP, NT-proBNP, proBNP1108, and Tyr0-proBNP77108. Fifteen peptides of 1322 amino acids, spanning the sequences of NT-proANP and NT-proBNP, were prepared by solid-phase peptide synthesis. Two immunoassays for NT-proANP and four for NT-proBNP were set up, each with a different epitope specificity. The assays were applied for the measurement of NT-proANP and NT-proBNP in healthy individuals and in patients with acute myocardial infarction. The circulating molecular forms were analyzed by gel-filtration and reversed-phase HPLC.
Results: According to the HPLC analyses, circulating NT-proANP consists mainly of the full-length peptide, with some degradation at both ends. In contrast, circulating NT-proBNP is very heterogeneous. Most immunoreactive NT-proBNP is significantly smaller in size than NT-proBNP176, with truncation at both termini. The smallest fragments can be detected by assays directed at the central part of NT-proBNP only; assays directed at the ends gave 3040% lower values. Despite the difference, the various assays correlated reasonably well with each other (r2 = 0.770.85). In patients with acute myocardial infarction, NT-proANP and NT-proBNP concentrations were 1.82.3 and 4.24.5 times higher than in healthy individuals. The development of heart failure further increased the concentrations.
Conclusions: Molecular heterogeneity of the circulating forms causes a serious risk of preanalytical errors in assays for NT-proBNP and, to a lesser extent, NT-proANP. The development of a sandwich assay for NT-proBNP would be especially challenging. The most robust and reliable assays use antibodies directed at the central portions of NT-proANP or NT-proBNP.
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