Methods for ligation and uses thereof
The present invention relates to methods for ligation. The invention provides novel reagents and methods for ligating an acyl donor compound with an acyl acceptor compound. Provided acyl donor compounds comprise a transamidase recognition sequence that allows ligation with a nucleophilic acyl acceptor in the presence of transamidase. The invention further provides kits comprising acyl donor compounds and optionally comprising other reagents for ligation.
1. A method of ligation comprising the step of contacting an acyl donor compound of formula:
wherein
the transamidase recognition sequence is LPXT, wherein the X of the recognition sequence is any natural or unnatural amino acid;
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 6, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula:
2. The method of claim 1 , wherein X is —O—.
3. The method of claim 1 , wherein the recognition sequence is LPXT, wherein the X of the recognition sequence is D, E, A, N, Q, K, or R.
4. The method of claim 1 , wherein the transamidase is sortase A.
5. The method of ligation of claim 1 comprising the step of contacting an acyl donor compound of formula:
wherein
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
R 2 is a natural or unnatural amino acid side chain;
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 100, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula:
6. A method of ligation comprising the step of contacting an acyl donor compound of formula:
wherein
the transamidase recognition sequence is selected from LPXT, SPXT, LAXT, LSXT, NPXT, VPXT, IPXT, and YPXR wherein the X of the recognition sequence is a natural or unnatural amino acid;
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 6, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula:
7. The method of claim 6 , wherein X is —O—.
8. The method of claim 6 , wherein the X of the recognition sequence is D, E, A, N, Q, K, or R.
9. The method of claim 6 , wherein the transamidase is sortase A.
10. The method of claim 6 , wherein the transamidase is sortase B.
11. The method of claim 6 comprising the step of contacting an acyl donor compound of formula:
wherein
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
R 2 is a natural or unnatural amino acid side chain;
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 100, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula:
12. A method of ligation comprising the step of contacting an acyl donor compound of formula:
wherein
the transamidase recognition sequence is selected from: LPKT (SEQ ID NO: 69), LPIT (SEQ ID NO: 70), LPDT (SEQ ID NO: 71), SPKT (SEQ ID NO: 72), LAET (SEQ ID NO: 73), LAAT (SEQ ID NO: 74), LAET (SEQ ID NO: 75), LAST (SEQ ID NO: 76), LAET (SEQ ID NO: 77), LPLT (SEQ ID NO: 78), LSRT (SEQ ID NO: 79), LPET (SEQ ID NO: 53), VPDT (SEQ ID NO: 80), IPQT (SEQ ID NO: 81), YPRR (SEQ ID NO: 82), LPMT (SEQ ID NO: 83), LPLT (SEQ ID NO: 84), LAFT (SEQ ID NO: 85), LPQT (SEQ ID NO: 86), NSKT (SEQ ID NO: 87), NPQT (SEQ ID NO: 88), NAKT (SEQ ID NO: 89), and NPQS (SEQ ID NO: 90);
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 6, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula:
13. The method of claim 12 , wherein X is —O—.
14. The method of claim 12 , wherein the transamidase is sortase A.
15. The method of claim 12 , wherein the transamidase is sortase B.
16. The method of claim 12 comprising the step of contacting an acyl donor compound of formula:
wherein
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
R 2 is a natural or unnatural amino acid side chain;
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 100, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula:
17. A method of ligation comprising the step of contacting an acyl donor compound of formula:
wherein
the transamidase recognition sequence is X 1 PX 2 X 3 , where X 1 is leucine, isoleucine, valine or methionine; X 2 is any amino acid; X 3 is threonine, serine or alanine; P is proline;
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 6, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula:
18. The method of claim 17 , wherein X is —O—.
19. The method of claim 17 , wherein the transamidase is sortase A.
20. The method of claim 17 , wherein the transamidase is sortase B.
21. The method of claim 17 comprising the step of contacting an acyl donor compound of formula:
wherein
A 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label;
X is —O— or —S—;
R is hydrogen, substituted or unsubstituted aliphatic, or substituted or unsubstituted heteroaliphatic;
R 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
R 2 is a natural or unnatural amino acid side chain;
with a nucleophilic compound of formula:
wherein
B 1 is acyl, substituted or unsubstituted aliphatic, substituted or unsubstituted heteroaliphatic, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a peptide, a protein, a polynucleotide, a carbohydrate, a tag, a metal atom, a contrast agent, a catalyst, a non-polypeptide polymer, a recognition element, a small molecule, a lipid, or a label; and
n is an integer from 0 to 100, inclusive;
in the presence of a transamidase enzyme under suitable conditions to form a compound of formula: