Cysteine arylation directed by a genetically encodable π-clamp
Disclosed are methods of single-site-specific cysteine modification on peptide/protein molecules under physiologically relevant conditions. This process features several significant advantages over existing methods of peptide modification, such as specificity towards thiols over other nucleophiles (e.g., amines, hydroxyls), excellent functional group tolerance, and mild reaction conditions. Especially important is the specificity observed for thiols appearing in an X-Cys-Pro-X sequence over other thiols or disulfides, where X is Phe, Trp, or Tyr; under the inventive conditions, other cysteines or reactive functional groups on the same peptide/protein chain are not functionalized.
1. A method according to Scheme 1:
wherein, independently for each occurrence,
base is a Bronsted base;
A 1 is H, an amine protecting group, a natural or unnatural alpha amino acid, a peptide, an oligopeptide, a polypeptide, or a protein;
A 5 is OH, —O(carboxylate protecting group), a natural or unnatural alpha amino acid, a peptide, an oligopeptide, a polypeptide, or a protein;
x is 0, 1, 2, 3, 4, 5, or 6;
R is H or alkyl;
R 2 is aralkyl or heteroaralkyl;
R 3 is aralkyl or heteroaralkyl;
{circle around (B)} is a perfluorinated aryl radical; and
is a perfluorinated aryl para-substituted diradical.
2. The method of claim 1 , wherein the base is triethylamine, Na 3 PO 4 , or tris(hydroxymethyl)aminomethane.
3. The method of claim 1 , wherein R 2 is benzyl, indolylmethyl, or hydroxybenzyl.
4. The method of claim 1 , wherein R 3 is benzyl, indolylmethyl, or hydroxybenzyl.
5. The method of claim 1 , wherein R is H.
6. The method of claim 1 , wherein x is 1, 2, or 3.
7. The method of claim 1 , wherein {circle around (B)} is pentafluorophenyl or 4′-(2,2′,3,3′,4,5,5′,6,6′-nonafluoro-1,1′-biphenyl).
8. The method of claim 1 , wherein {circle around (B)} comprises at least one 18 F isotope.
9. A compound comprising substructure I or substructure II:
wherein, independently for each occurrence,
A 1 is H, an amine protecting group, a natural or unnatural alpha amino acid, a peptide, an oligopeptide, a polypeptide, or a protein;
A 5 is OH, —O(carboxylate protecting group), a natural or unnatural alpha amino acid, a peptide, an oligopeptide, a polypeptide, or a protein;
{circle around (B 1 )} is a perfluorinated aryl para-substituted diradical;
x is 0, 1, 2, 3, 4, 5, or 6;
R is H or alkyl;
R 1 is H, alkyl, thioalkyl, alkylthioalkyl, aralkyl, heteroaralkyl, hydroxyaralkyl, HO 2 C-alkyl, H 2 N—C(O)-alkyl, heterocycloalkyl, guanidinylalkyl, aminoalkyl, or hydroxyalkyl;
R 2 is aralkyl or heteroaralkyl; and
R 3 is aralkyl or heteroaralkyl.
10. The compound of claim 9 , wherein R 2 is benzyl, indolylmethyl, or hydroxybenzyl.
11. The compound of claim 9 , wherein R 3 is benzyl, or indolylmethyl, or hydroxybenzyl.
12. The compound of claim 9 , wherein {circle around (B 1 )} is 2,3,5,6-tetrafluorophenylene or 2,2′,3,3′,5,5′,6,6′-octafluoro-1,1′-biphenyl-4,4′-ene.
13. The compound of claim 9 , wherein R is H.
14. The compound of claim 9 , wherein x is 1, 2, or 3.
15. The compound of claim 9 , wherein the compound comprises a substructure selected from the group consisting of (peptides disclosed as SEQ ID NOS 1-2, respectively, in order of appearance):
16. The compound of claim 9 , wherein the compound comprises a substructure selected from the group consisting of (peptides disclosed as SEQ ID NOS 1-2, respectively, in order of appearance):
17. The compound of claim 9 , wherein {circle around (B 1 )} comprises at least one 18 F isotope.