Page last updated: 2024-12-11

(2-sulfonatoethyl)methanethiosulfonate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

**(2-Sulfonatoethyl)methanethiosulfonate (MTSES)** is a chemical compound that is used in biological research to modify proteins and enzymes.

**Structure and Properties:**

* **Chemical Formula:** C3H7O6S3Na
* **Molecular Weight:** 252.22 g/mol
* **Appearance:** White solid
* **Solubility:** Soluble in water
* **Reactivity:** Reacts with sulfhydryl groups (-SH) in proteins and enzymes

**Mechanism of Action:**

MTSES contains a methanethiosulfonate group (MTS) that reacts with the sulfhydryl groups of cysteine residues in proteins. This reaction results in the formation of a stable thioether bond, effectively modifying the protein.

**Applications in Research:**

MTSES is used in various research areas, including:

* **Protein Structure and Function:** MTSES can be used to label and identify cysteine residues in proteins, providing insights into their structure and function.
* **Enzyme Activity:** MTSES can be used to modify cysteine residues that are crucial for enzyme activity. By modifying these residues, researchers can study the role of specific cysteine residues in enzyme catalysis.
* **Protein-Protein Interactions:** MTSES can be used to probe protein-protein interactions by modifying cysteine residues involved in these interactions.
* **Cell Signaling Studies:** MTSES can be used to modify cysteine residues in signaling proteins, allowing researchers to study the role of these proteins in signal transduction pathways.

**Advantages of MTSES:**

* **Specificity:** MTSES is relatively specific for cysteine residues and does not react with other amino acids.
* **Stability:** The thioether bond formed by MTSES is stable under physiological conditions.
* **Water-Solubility:** MTSES is water-soluble, making it suitable for use in aqueous solutions.

**Limitations:**

* **Reactivity:** MTSES can react with other sulfhydryl-containing molecules, potentially leading to off-target modifications.
* **Accessibility:** MTSES may not be able to access all cysteine residues in a protein due to steric hindrance or other factors.

**Conclusion:**

(2-Sulfonatoethyl)methanethiosulfonate (MTSES) is a valuable tool for researchers studying protein structure, function, and interactions. Its ability to modify cysteine residues in a specific and stable manner makes it a versatile reagent for a wide range of applications. However, its limitations should be considered when designing experiments.

(2-sulfonatoethyl)methanethiosulfonate: RN given for Na salt [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID23688468
MeSH IDM0283357

Synonyms (8)

Synonym
(2-sulfonatoethyl)methanethiosulfonate
2-((methylthio)sulfonyl)ethanesulfonic acid sodium salt
mtses cpd
methanethiosulfonate ethylsulfonate
ethanesulfonic acid, 2-((methylthio)sulfonyl)-, sodium salt
sodium;2-methylsulfanylsulfonylethanesulfonate
J4SU48UKA9
ethanesulfonic acid, 2-[(methylthio)sulfonyl]-, sodium salt

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" Dose-response analysis showed that treatment with MTSET increased the potency of the FMRFamide in the FaNaC whereas treatment with MTSES reduced the maximum response."( Electrostatic charge at position 552 affects the activation and permeation of FMRFamide-gated Na+ channels.
Furukawa, Y; Kodani, Y, 2014
)
0.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (85)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's10 (11.76)18.2507
2000's55 (64.71)29.6817
2010's20 (23.53)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other86 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]