SML3140
GsMTx4 trifluoroacetate
≥95% (HPLC), powder, TRPC1 and TRPC6 inhibitor
Sinônimo(s):
1-amino-Cy5-glucose, Cyanine-based 1-amino-1-deoxy-β-glucose conjugate, Cy5-linked 1amino-glucose, GCLEFWWKCNPNDDKCCRPKLKCSKLFKLCNFSF-NH2 trifluoroacetate(Disulfide: 2-17, 9-23, 16-30), Gly-Cys-Leu-Glu-Phe-Trp-Trp-Lys-Cys-Asn-Pro-Asn-Asp-Asp-Lys-Cys-Cys-Arg-Pro-Lys-Leu-Lys-Cys-Ser-Lys-Leu-Phe-Lys-Leu-Cys-Asn-Phe-Ser-Phe-NH2 trifluoroacetate (Disulfide: 2-17, 9-23, 16-30), Grammostola Mechanotoxin #4 trifluoroacetate, GsMTx-4 trifluoroacetate, L-GsMTx trifluoroacetate
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About This Item
Código UNSPSC:
12352200
NACRES:
NA.77
Produtos recomendados
product name
GsMTx4 trifluoroacetate, ≥95% (HPLC)
Nível de qualidade
Ensaio
≥95% (HPLC)
forma
powder
cor
white to beige
temperatura de armazenamento
−20°C
Descrição geral
Grammostola mechanotoxin #4 (GsMTx4), a gating modifier peptide, is obtained from spider venom. This 34-amino-acid peptide is a small (3-5 kD) amphipathic molecule built on a conserved inhibitory cysteine-knot (ICK) backbone. The structure of GsMTx4 has a belt of charged residues surrounding a hydrophobic patch. GsMTx4 acts as an inhibitor of cationic mechanosensitive channels (MSCs) belonging to the Piezoand transient receptor potential (TRP) channel families. It is different from other spider venom peptides because it can inhibit these channels regardless of their shape, and both its L- and D-forms can have this effect. GsMTx4 has a unique structure and carries a positive charge due to its six lysine residues which can affect membrane binding. This peptide has become a valuable tool in research to identify the roles of excitatory MSCs in normal physiology and pathology. It can also inhibit stretch-activated big potassium channels (SAKcaC). The presence of positively charged residues in GsMTx4 is thought to play a role in peptide channel-lipid interaction. It can effectively reduce arrhythmias by inhibiting stretch-activated channels (SACs) in the heart. GsMTx4 also serves as an inhibitor of histone acetylation inhibitor I-BET 762 and Piezo 1 inhibitor.
Aplicação
GsMTx4 trifluoroacetate has been used in drug treatment as a supplement in cell culture medium to treat mouse hippocampal neurons to block cationic MSCs in cortical neurons. It has also been used as a specific inhibitor to incubate cementoblasts to study its effects on the response of cementoblasts to investigate if cementum repair was impaired by compression.
Ações bioquímicas/fisiológicas
GsMTx4 (Grammostola Mechanotoxin #4) is a tarantula venom-derived 34-mer amphipathic cysteine knot peptide that exerts its cationic mechanosensitive channels (MSCs; stretch-gated ion channels or SACs) modulatory activity by changing local membrane properties near the channels. GsMTx4 negatively regulates TRPC1/5/6 and Piexo1/2, while potentiating TREK-1 and TRPA1 activity. In addition, GsMTx4 can either hamper (2-4 μM) or facilitate (12-20 μM) the gating of prokaryotic E. coli cytoplasmic membrane MscS and MscK in a biphasic manner. GsMTx4 is also reported to inhibit Nav1.1 (SCN1A), Nav1.2 (SCN2A), Nav1.3 (SCN3A), Nav1.4 (SCN4A), Nav1.5 (SCN5A), Nav1.6 (SCN8A), Nav1.7 (SCN9A), hERG1/2/3 (KCNH2/6/7), but not hKV1.1 (KCNA1) or hKV1.4 (KCNA4).
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Certificados de análise (COA)
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T M Suchyna et al.
The Journal of general physiology, 115(5), 583-598 (2000-04-25)
We have identified a 35 amino acid peptide toxin of the inhibitor cysteine knot family that blocks cationic stretch-activated ion channels. The toxin, denoted GsMTx-4, was isolated from the venom of the spider Grammostola spatulata and has <50% homology to
Annette C Hurst et al.
European biophysics journal : EBJ, 38(4), 415-425 (2009-01-10)
The spider peptide GsMTx4, at saturating concentration of 5 muM, is an effective and specific inhibitor for stretch-activated mechanosensitive (MS) channels found in a variety of eukaryotic cells. Although the structure of the peptide has been solved, the mode of
Kerstin Hill et al.
The Journal of biological chemistry, 282(10), 7145-7153 (2007-01-16)
TRPA1, a poorly selective Ca(2+)-permeable cation channel, is expressed in peripheral sensory neurons, where it is considered to contribute to a variety of sensory processes such as the detection of painful stimuli. Furthermore, TRPA1 was also identified in hair cells
GsMTx4: Mechanism of Inhibiting Mechanosensitive Ion Channels
Gnanasambandam R, et al.
Biophysical Journal, 31-45 (2017)
A Fabian et al.
Pflugers Archiv : European journal of physiology, 457(2), 475-484 (2008-06-11)
Cell migration depends on the generation of structural asymmetry and on different steps: protrusion and adhesion at the front and traction and detachment at the rear part of the cell. The activity of Ca(2+) channels coordinate these steps by arranging
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