GLPBio

Mastoparan

Catalog No.: GC12692Purity:>98.00%
Mastoparan, ein Tetradecapeptid, das ein Bestandteil von Wespengift ist, stimuliert die Freisetzung von Prolactin aus kultivierten Hypophysenvorderlappenzellen der Ratte.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Mastoparan
Cas No.: 72093-21-1
1mgIn Stock
$63.00
1
5mgIn Stock
$158.00
1
10mgIn Stock
$245.00
1

Zitate (Citations)

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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Mastoparan, a peptide toxin from wasp venom, induces stimulation of phosphoinositide breakdown with an EC50 value of 9μM[1]. Mastoparan accelerates guanosine-5'-3-O-thiotriphosphate binding and consequent GTP-binding regulatory protein (G protein) activation in part by enhancing the dissociation of bound GDP[2]. Mastoparan has been widely used in anti-inflammatory studies and as a model compound to develop related derivatives[3].

In vitro, Mastoparan exhibited an anticancer towards Hep-G2 cells with IC50=189.59±0.6µg/ml after 24h treatment[4]. Treatment with 25μM Mastoparan for 8h significantly induced cell death in Jurkat T leukemia cells and normal peripheral blood cells[5]. Mastoparan treatment at 20μM within 1min significantly induced a rapid increase in cytosolic-free Ca2+ concentration elevation in Tobacco BY-2 cells[6].

In vivo, Mastoparan treatment via a peritumor route at 5 mg/kg/day for 5 consecutive days inhibited the tumor growth in the murine melanoma model[7]. The combination therapy of gemcitabine (60mg/kg/day) and Mastoparan (6mg/kg/day) for 14 days via intraperitoneal injection significantly inhibited tumor progression in a mouse model of breast cancer[5].

References:
[1] Gusovsky F, Soergel D G, Daly J W. Effects of mastoparan and related peptides on phosphoinositide breakdown in HL-60 cells and cell-free preparations[J]. European Journal of Pharmacology: Molecular Pharmacology, 1991, 206(4): 309-314.
[2] Higashijima T, Uzu S, Nakajima T, et al. Mastoparan, a peptide toxin from wasp venom, mimics receptors by activating GTP-binding regulatory proteins (G proteins)[J]. Journal of Biological Chemistry, 1988, 263(14): 6491-6494.
[3] Chen X, Zhang L, Wu Y, et al. Evaluation of the bioactivity of a mastoparan peptide from wasp venom and of its analogues designed through targeted engineering[J]. International journal of biological sciences, 2018, 14(6): 599.
[4] Elsharkawy A M, Galhom R A, Amin B H, et al. In Vitro Evaluation of Some Therapeutic Applications of Wasp Venom and Mastoparan[J]. Egyptian Academic Journal of Biological Sciences. A, Entomology, 2024, 17(1): 121-130.
[5] Hilchie A L, Sharon A J, Haney E F, et al. Mastoparan is a membranolytic anti-cancer peptide that works synergistically with gemcitabine in a mouse model of mammary carcinoma[J]. Biochimica Et Biophysica Acta (BBA)-Biomembranes, 2016, 1858(12): 3195-3204.
[6] Takahashi K, Isobe M, Muto S. Mastoparan induces an increase in cytosolic calcium ion concentration and subsequent activation of protein kinases in tobacco suspension culture cells[J]. Biochimica et Biophysica Acta (BBA)-Molecular Cell Research, 1998, 1401(3): 339-346.
[7] de Azevedo R A, Figueiredo C R, Ferreira A K, et al. Mastoparan induces apoptosis in B16F10-Nex2 melanoma cells via the intrinsic mitochondrial pathway and displays antitumor activity in vivo[J]. Peptides, 2015, 68: 113-119.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

Immortalized human dermal microvessel endothelial cells

Preparation Method

The growth of immortalized human dermal microvessel endothelial cells (HMECs) occurred in MCDB-131 medium which contained 10% inactivated FBS and 2mM glutamine as well as 100U/ml penicillin and 100μg/ml streptomycin. HMECs were seeded in 24-well culture plates (approximate cell density, 3×105 cells/well) containing medium supplemented with 5% heat-inactivated FBS. After cells reached confluence, cells were stimulated for 6h with lipopolysaccharide (LPS) at 10ng/ml, with or without a 30min preincubation of cells with Mastoparan (0, 5, 10, 15, 20, and 25μM). Supernatants were harvested and assayed for IL-6 activity by ELISA.

Reaction Conditions

0, 5, 10, 15, 20, and 25μM; 30min

Applications

Mastoparan exerted a dose-dependent inhibition on the expression and secretion of IL-6 induced by LPS.
Animal experiment [2]:

Animal models

C57BL/6 mice

Preparation Method

At 6 to 8 weeks of age of male C57BL/6 mice, 5×104 viable B16F10-Nex2 cells were subcutaneously (s.c.) inoculated on the right side of male C57BL/6 mice. When the tumor reached a volume of 100mm3, the mice received 5 weekly intratumoral doses of Mastoparan (5mg/kg/day). The untreated tumor control group received 100μL PBS. After administration of the therapeutic dose, the tumor size was measured daily using a caliper. The tumor volume (V) was calculated using the formula V=0.52×d2×D, where d and D are the short and long diameters of the tumor, respectively. When the tumor size reached a maximum of 3000mm3, the animals were sacrificed for subsequent experimental analysis.

Dosage form

5mg/kg/day for 5 weeks a day; i.t.

Applications

Mastoparan treatment inhibited the growth of subcutaneous melanoma in mice and increased the survival rate.

References:
[1] Lentschat A, Karahashi H, Michelsen K S, et al. Mastoparan, a G protein agonist peptide, differentially modulates TLR4-and TLR2-mediated signaling in human endothelial cells and murine macrophages[J]. The Journal of Immunology, 2005, 174(7): 4252-4261.
[2] de Azevedo R A, Figueiredo C R, Ferreira A K, et al. Mastoparan induces apoptosis in B16F10-Nex2 melanoma cells via the intrinsic mitochondrial pathway and displays antitumor activity in vivo[J]. Peptides, 2015, 68: 113-119.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
72093-21-1
Chemischer Name
(S,Z)-2-((Z)-((2S,3S)-2-amino-1-hydroxy-3-methylpentylidene)amino)-N'1-((4S,5Z,7S,8Z,10S,11Z,13S,14Z,16S,17Z,19S,20Z,22S,23Z,25S,26Z,28S,29Z,31S,32Z,34S,35Z,37S)-10,13,34-tris(4-aminobutyl)-7-((S)-sec-butyl)-6,9,12,15,18,21,24,27,30,33,36-undecahydroxy-4-
SMILES
CC[C@]([C@@](N)([H])/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](C(O)=N)([H])CC(C)C)([H])[C@@](CC)([H])C)([H])CCCCN)([
Summenformel
C70H131N19O15
Molekulargewicht
1479
Löslichkeit
Soluble to 2.60 mg/ml in sterile water
Lagerung
Desiccate at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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