Hidehisa Asada

Molecular forms of human brain natriuretic peptide in plasma.

BACKGROUND Brain natriuretic peptide (BNP) is a vasoreactive peptide hormone, which is synthesized and secreted mainly from the heart ventricles. METHODS Molecular forms of immunoreactive human brain natriuretic peptide (BNP) were examined. Chemically synthesized human BNP was added to whole blood samples from a healthy volunteer. The immunoreactive peptide was recovered by immunoaffinity chromatography followed by reversed-phase HPLC (RP-HPLC). Molecular form of immunoreactive BNP in plasma from heart failure patients was also examined. RESULTS Sequential analysis and amino acid analysis of the peptide revealed that two amino acid residues were deleted from the amino terminus of BNP. When roughly classified according to molecular weight (MW), two forms of BNP (high-MW BNP and low-MW BNP) were observed. The estimated MW of high-MW BNP (36 kDa) was three times that of pro-BNP (12 kDa). CONCLUSIONS Analysis of low-MW BNP by RP-HPLC revealed that a small amount of BNP 1-32 or des-SerPro-BNP (BNP 3-32) was contained in plasma from heart failure patients.

Characterization of molecular forms of probrain natriuretic peptide in human plasma

BACKGROUND Measurement of brain natriuretic peptide (BNP) in plasma is useful for the diagnosis and prognosis of heart failure. However, the molecular forms of BNP, especially proBNP in the blood, have been poorly characterized. METHODS To investigate the forms of proBNP in blood, antibodies against four proBNP synthetic peptides (1-13, 22-27, 28-40, and 47-54) were developed and characterized for their reactivity to proBNP by ELISA. Using the antibodies and a monoclonal antibody specific to the carboxyl terminal histidine of BNP, a radioimmunoassay for proBNP was constructed. BNPs in plasma from heart failure patients were analyzed by gel-filtration HPLC followed by immunoassay for BNP and proBNP. RESULTS Two of four antibodies against proBNP synthetic peptides reacted with both r-proBNP and BNP in plasma from the patients. Gel-filtration HPLC analysis showed two major peaks of immunoreactive BNP (high MW BNP (36 kDa) and low MW BNP (4 kDa)). The immunoassay demonstrated that almost the full-length of proBNP was contained in the high MW BNP fractions. CONCLUSIONS ProBNP was more stable than its mature form of BNP in circulation after secretion, and it suggested the usefulness of proBNP measurement.