BNP (B-type Natriuretic Peptide)

Cardiovascular
Chemical Profile
Molecular Formula
C143H244N50O42S4
Molar Mass
3,464.08 g/mol
CAS Number
114471-18-0
Purity Standard
99%+ (HPLC Verified)
Amino Acid Sequence
Ser-Pro-Lys-Met-Val-Gln-Gly-Ser-Gly-Cys-Phe-Gly-Arg-Lys-Met-Asp-Arg-Ile-Ser-Ser-Ser-Ser-Gly-Leu-Gly-Cys-Lys-Val-Leu-Arg-Arg-His (32-amino acid with Cys10-Cys26 disulfide ring)

Overview

B-type natriuretic peptide (BNP, also called brain natriuretic peptide based on initial identification site) is a 32-amino acid cardiac hormone secreted primarily by ventricular cardiomyocytes in response to wall stretch and volume overload. It serves as both a physiological regulator of cardiovascular homeostasis and a clinically valuable biomarker for heart failure.

BNP acts through natriuretic peptide receptor A (NPR-A), a guanylyl cyclase-coupled receptor that increases intracellular cGMP. This signaling cascade produces vasodilation, natriuresis, diuresis, and inhibition of the renin-angiotensin-aldosterone system - effects that counteract the fluid retention and vasoconstriction characteristic of heart failure.

Clinically, BNP and its inactive N-terminal fragment (NT-proBNP) are established biomarkers for heart failure diagnosis, risk stratification, and management. Elevated levels indicate cardiac wall stress and correlate with heart failure severity and prognosis. Point-of-care BNP testing enables rapid differentiation of cardiac from pulmonary causes of dyspnea.

Research applications include studying heart failure pathophysiology, investigating natriuretic peptide receptor signaling, developing improved cardiac biomarkers, and understanding the interplay between cardiac and renal function in cardiorenal syndrome. BNP levels also provide insight into cardiac effects of various therapeutic interventions.

Synthesis Overview

BNP is synthesized via Fmoc solid-phase peptide synthesis as a 32-amino acid sequence containing two cysteine residues that form an intramolecular disulfide bond creating a 17-amino acid ring structure characteristic of natriuretic peptides. The two methionine residues require protection against oxidation. Following linear chain assembly and cleavage, controlled oxidation forms the Cys10-Cys26 disulfide bond. Purification via preparative HPLC separates correctly folded BNP from misfolded or oxidized species. Biological activity is confirmed through natriuretic peptide receptor binding or cGMP stimulation assays.

Research Applications

  • Heart failure pathophysiology and ventricular function research
  • Cardiac biomarker diagnostic development studies
  • Natriuretic peptide receptor (NPR-A/B) signaling investigation
  • cGMP-mediated vasodilation and natriuresis mechanism research
  • Cardiorenal syndrome and fluid homeostasis studies
  • Cardiac remodeling and neurohormonal activation research

Related Compounds