E5763
Escherichia coli heat-stable enterotoxin STa
lyophilized powder, ~100,000 units/mg protein (HPLC)
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UNSPSC Code:
12352200
MDL number:
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Servicio técnico
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lyophilized powder
specific activity
~100,000 units/mg protein (HPLC)
mol wt
1,972 Da
solubility
aqueous buffer: ≥5 mg/mL (More soluble under acidic conditions)
storage temp.
−20°C
Biochem/physiol Actions
STa has a tertiary structure, maintained by disulfide bridges, which is required for receptor binding and biological activity. Its receptors are membrane-bound guanylyl cyclases. These receptors are located on enterocytes, colonocytes, and various extraintestinal tissues. STa causes diarrhea in humans by binding to its receptor, stimulating the guanylyl cyclase, and triggering production of cyclic GMP. Endogenous ligands for the STa receptor include guanylin, extracted from intestine, and uroguanylin from urine. These peptides may have a role in the regulation of fluid and electrolytes. Protein kinase C (PKC) phosphorylates and activates the STa receptor/guanylyl cyclase in vitro and in vivo. As a result, stimulators of PKC synergistically enhance STa effects on cGMP and secretion.
Other Notes
E. coli STa is a heat-stable peptide toxin.
One unit is the amount of toxin which produces an intestinal weight/carcass weight ratio of ≥0.083 in 3-day-old mice.
Clase de almacenamiento
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Contenido relacionado
Product Information Sheet
R A Giannella
The Journal of laboratory and clinical medicine, 125(2), 173-181 (1995-02-01)
STa represents a family of homologous heat-stable peptide toxins that are elaborated by a variety of bacteria capable of causing enteric disease in human beings. All these peptides have a tertiary structure, maintained by disulfide bridges, which is required for
J K Crane et al.
Molecular and cellular biochemistry, 165(2), 111-120 (1996-12-20)
The heat-stable enterotoxin STa of E. coli causes diarrhea by binding to and stimulating intestinal membrane-bound guanylyl cyclase, triggering production of cyclic GMP. Agents which stimulate protein kinase C (PKC), including phorbol esters, synergistically enhance STa effects on cGMP and
S P Range et al.
British journal of pharmacology, 120(7), 1249-1254 (1997-04-01)
1. Guanosine 3':5'-cyclic monophosphate (cyclic GMP) is an important second messenger mediating the effects of nitric oxide (NO) and natriuretic peptides. Cyclic GMP pathways regulate several aspects of lung pathophysiology in a number of airway cells. The regulation of this