Target intelligence / Profile preview

Chromogranin B (CHGB)

Target
CHGB
Molecular classification
Other (granule matrix protein of the granin family), Ion channel (forms large-conductance chloride channels in membranes)[2][3]
01

Overview

Chromogranin B (CHGB) is a member of the granin family of acidic proteins highly expressed in neuroendocrine cells, where it is the principal matrix protein of secretory vesicles (such as chromaffin and large dense-core granules)[1][2]. It is essential for the biogenesis and regulated secretion of these granules, modulating the storage and release of catecholamines (like adrenaline and noradrenaline). CHGB also exists in both soluble and membrane-bound forms; notably, the membrane-integrated form can assemble into large-conductance, highly selective chloride channels, contributing to anion homeostasis and potentially plasma membrane and granule membrane physiology[2][3]. Beyond trafficking and storage roles, proteolytic processing of CHGB generates bioactive peptides that act in autocrine signaling. Abnormal CHGB expression or function is associated with diseases such as hypertension, neurodegeneration, and psychiatric disorders, making it a protein of interest in neuroendocrine and cardiovascular research[1][2][3]. There are currently no drugs known to clinically target CHGB directly, though research tools like ion channel inhibitors exist for experimental modulation[3].

Other names
Secretogranin-1PE-11GAWK peptideCCB peptideSCG1CgBSgIChromogranin-BSecretogranin Isecretogranin Bsecretogranin-1cgBsgI
02

Mechanism of action

Not directly targeted by drugs clinically, but DIDS and similar inhibitors can block its anion channel activity experimentally[3]

03

Biological functions

Granule biogenesis and sorting in neuroendocrine secretory vesicles[1][2]Regulation of catecholamine storage and release[1]Formation of membrane-associated anion (chloride) channels affecting ion homeostasis[2][3]Source of bioactive peptides with signaling roles[1]Ca²⁺ sequestration and release[1]
04

Disease associations

Hypertension (due to altered catecholamine secretion)[1]Neurodegenerative diseases, such as Alzheimer disease[1]Schizophrenia and other diseases with neurotransmitter storage/release defects[1]Potential links to other catecholaminergic disorders[3]
05

Safety considerations

Therapeutic targeting not established; interfering with CHGB function could impair catecholamine storage, risking dysregulation of blood pressure, stress response, and neurotransmission[1]
06

Interacting drugs

None specifically identified in the literature as direct targeting agents[3]

1 more in the full profile.

07

Biomarkers

Altered CHGB expression has been investigated as a biomarker in conditions affecting catecholamine storage or neurodegenerative diseases[1]

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