Methods for assaying enzyme activities
View Patent ↗The present invention provides compounds and methods for assaying activities of enzymes such as histone deacetylases and histone acetyltransferases. In some embodiments, the methods may be performed in one step. The compounds described herein features peptide-based compounds having at least one blocked lysine or arginine residue which are coupled to reporter moieties. The methods described herein involve reacting a compound described herein with an enzyme, such as a histone deacetylase enzyme or a histone acetyltransferase enzyme, and an endopeptidase that recognizes basic amino acids to release the reporter moiety which may be subsequently detected.
1. A compound of formula (I):
wherein:
A is
R 1 is selected from H, an amino protecting group and an amino blocking group;
n is an integer from 1 to 20;
each R 2 is independently an amino acid side chain, wherein at least one R 2 is selected from —CH 2 —CH 2 —CH 2 —CH 2 —NR 4a R 4b , —CH 2 —CH 2 —CH 2 CH 2 —N + R 4a R 4b R 4c and —CH 2 —CH 2 —CH 2 —NH—C(═NR 5a )NR 5b R 5c ;
R 3 is acyl;
each R 4a is independently selected from hydrogen, alkyl and aryl;
each R 4b is independently selected from alkyl and aryl;
each R 4c is independently selected from hydrogen, alkyl and aryl;
each R 5a is independently selected from hydrogen, alkyl and aryl;
each R 5b is independently selected from alkyl and aryl; and
each R 5c is independently selected from hydrogen, alkyl and aryl,
wherein when R 2 is —CH 2 —CH 2 —CH 2 —CH 2 —N + R 4a R 4b R 4c , the compound further comprises a counteranion.
2. The compound of claim 1 , wherein R 1 is an amino protecting group or an amino blocking group selected from the group consisting of 9-fluorenylmethyloxycarbonyl (Fmoc), carbobenzyloxy (Cbz), tertbutyloxy (Boc), acetyl and succinyl.
3. The compound of claim 1 , wherein n is 2, 3, 4 or 5.
4. The compound of claim 1 , wherein at least one R 2 is selected from —CH 2 —CH 2 —CH 2 —CH 2 —NH—CH 3 , —CH 2 —CH 2 —CH 2 —CH 2 —N(CH 3 ) 2 , —CH 2 —CH 2 —CH 2 —CH 2 —N + (CH 3 ) 3 and —CH 2 —CH 2 —CH 2 —NH—C(═NH)NHCH 3 .
5. The compound of claim 1 , wherein R 3 is selected from acetyl and trifluoroacetyl.
6. The compound of claim 1 , wherein the compound is selected from:
7. A method of detecting the activity of a histone deacetylase enzyme, comprising:
a) reacting the compound according to claim 1 with a histone deacetylase enzyme and an endopeptidase that recognizes basic amino acids, under conditions sufficient to allow the histone deacetylase enzyme to react with the compound of formula (I) to form a product, and the endopeptidase to react with the product to release a compound A-NH 2 ; and
b) detecting the compound A-NH 2 .
8. The method of claim 7 , further comprising correlating the detection of the compound A-NH 2 with the activity of the histone deacetylase enzyme.
9. The method of claim 8 , wherein the activity of the histone deacetylase enzyme is quantified.
10. The method of claim 7 , wherein the endopeptidase does not react with the compound of formula (I).
11. The method of claim 7 , wherein the product has the following formula (II):
12. The method of claim 7 , wherein the value of n and the identity of each R 2 moiety are chosen to confer specificity for the histone deacetylase enzyme.
13. The method of claim 7 , wherein the endopeptidase that recognizes basic amino acids is trypsin.
14. A composition comprising:
a. the compound according to claim 1 ,
b. an endopeptidase that recognizes basic amino acids, and
c. optionally, a detection reagent.
15. A kit comprising:
a. the compound according to claim 1 ,
b. an endopeptidase that recognizes basic amino acids, and
c. optionally, a detection reagent.