
iodoacetamide
Sign in to saveAlso known as 2-iodoacetamide
Iodoacetamide (IAA) is an organic compound with the chemical formula . It is an alkylating agent used for peptide mapping purposes. Its actions are similar to those of iodoacetate. It is commonly used to bind covalently with the thiol group of cysteine so the protein cannot form disulfide bonds. It is also used in ubiquitin studies as an inhibitor of deubiquitinase enzymes (DUBs) because it alkylates the cysteine residues at the DUB active site.
Research
3,675 papers- Iodoacetamide blank compensation in FXIII functional assays: Is it still necessary?International journal of laboratory hematology · 2023
- Alkylation of Galectin-1 with Iodoacetamide and Mass Spectrometric Mapping of the Sites of Incorporation.Methods in molecular biology (Clifton, N.J.) · 2022
- Isotopically-Labeled Iodoacetamide-Alkyne Probes for Quantitative Cysteine-Reactivity Profiling.Molecular pharmaceutics · 2018
- Iodoacetamide-induced artifact mimics ubiquitination in mass spectrometry.Nature methods · 2008
- Antibody-decorated chitosan-iodoacetamide-coated nanocarriers for the potential delivery of doxorubicin to breast cancer cells.International journal of biological macromolecules · 2024
via PubMed
Wikidata facts
- Mass
- 184.933762
Show 4 more facts
- chemical formula
- C₂H₄INO
- canonical SMILES
- C(C(=O)N)I
- melting point
- 93.5
- Commons category
- Iodoacetamide
via Wikidata · CC0
~2 min read
Article
4 sectionsContents
- Peptidase inhibitor
- Protein mass spectrometry
- References
- External links
Iodoacetamide (IAA) is an organic compound with the chemical formula . It is an alkylating agent used for peptide mapping purposes. Its actions are similar to those of iodoacetate. It is commonly used to bind covalently with the thiol group of cysteine so the protein cannot form disulfide bonds. It is also used in ubiquitin studies as an inhibitor of deubiquitinase enzymes (DUBs) because it alkylates the cysteine residues at the DUB active site.
==Peptidase inhibitor== Iodoacetamide is an irreversible inhibitor of all cysteine peptidases, with the mechanism of inhibition occurring from alkylation of the catalytic cysteine residue (see schematic). In comparison with its acid derivative, iodoacetate, iodoacetamide reacts substantially faster. This observation appears contradictory to standard chemical reactivity, however the presence of a favourable interaction between the positive imidazolium ion of the catalytic histidine and the negatively charged carboxyl-group of the iodoacetate is the reason for the increased relative activity of iodoacetamide. thumb|left|500px|Mechanism of irreversible inhibition of cysteine peptidases with iodoacetamide.