Tosyl phenylalanyl chloromethyl ketone

Tosyl phenylalanyl chloromethyl ketone
Identifiers
CAS Number	402-71-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	388718 ;
ECHA InfoCard	100.006.323
MeSH	Tosylphenylalanyl+Chloromethyl+Ketone
PubChem CID	439647;
UNII	P598716LJT ;
CompTox Dashboard (EPA)	DTXSID60883376 ;
	InChI InChI=1S/C17H18ClNO3S/c1-13-7-9-15(10-8-13)23(21,22)19-16(17(20)12-18)11-14-5-3-2-4-6-14/h2-10,16,19H,11-12H2,1H3/t16-/m0/s1 Key: MQUQNUAYKLCRME-INIZCTEOSA-N ; InChI=1/C17H18ClNO3S/c1-13-7-9-15(10-8-13)23(21,22)19-16(17(20)12-18)11-14-5-3-2-4-6-14/h2-10,16,19H,11-12H2,1H3/t16-/m0/s1 Key: MQUQNUAYKLCRME-INIZCTEOBY;
	SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](Cc2ccccc2)C(=O)CCl;
Properties
Chemical formula	C17H18ClNO3S
Molar mass	351.848 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Tosyl phenylalanyl chloromethyl ketone (TPCK) is a protease inhibitor. Its structural formula is 1-chloro-3-tosylamido-4-phenyl-2-butanone.

Uses

TPCK is an irreversible inhibitor of chymotrypsin. Also inhibits some cysteine proteases such as caspase, papain, bromelain or ficin.[1] It does not inhibit trypsin or zymogens.

TPCK is observed covalently bound in the active site of Caspase 3 in the crystal structure of the complex solved in 2010.[2] The chloromethyl group reacts with the active site cysteine to form a covalent bond with the loss of the chlorine.

TPCK is chosen for the chemical labelling of active histidine in enzyme analysis. The phenylalanine moiety is bound to the enzyme because of specificity for aromatic amino acid residues at the active site (as in chymotrypsin, in which it binds to the Histidine-57 residue in the active site).[3]

Virology

TPCK-treated trypsin is used to improve infection yield in laboratory tissue culture of some wild virus isolates that are not well-adapted to growth in vitro, such as some low-pathogenic avian influenza strains or fresh clinical isolates of SARS-CoV-2. The trypsin performs the maturation cleavage of the viral envelope proteins efficiently.

gollark: I decided to see exactly what all the random HTTP requests to stuff like `/wp-admin/index.php` and all that are trying to do, so I've made a script to log the headers, POST body and stuff so I can investigate later.

gollark: Did viruses never scan sequentially for whatever reason?

gollark: That's an odd distinction.

gollark: Well, I assume they expect it to be resolved in their favour somehow.

gollark: Epic tried to get around Apple's app store fees somehow.

References

Focus Biomolecules Catalog # 10-2290 TPCK. , Retrieved on May 23. 2013.
Ganesan et al. Acta Crystallogr F v67 p 842. PDB Entry 2xyg
Farrell, Shawn O.; Campbell, Mary K. (2006). Biochemistry. Australia: Thomson Brooks/Cole. p. 160. ISBN 0-534-39499-X.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Focus Biomolecules Catalog # 10-2290 TPCK. , Retrieved on May 23. 2013.

[2] Ganesan et al. Acta Crystallogr F v67 p 842. PDB Entry 2xyg

[isbn0-534-39499-x-3] Farrell, Shawn O.; Campbell, Mary K. (2006). Biochemistry. Australia: Thomson Brooks/Cole. p. 160. ISBN 0-534-39499-X.