Selective photoactivation of amino acids for single step peptide coupling
Disclosed herein are formulations, substrates, and arrays for amino acid and peptide synthesis on microarrays. In certain embodiments, methods for manufacturing and using the formulations, substrates, and arrays including one-step coupling, e.g., for synthesis of peptides in a C→N orientation are disclosed. In some embodiments, disclosed herein are formulations and methods for high efficiency coupling of biomolecules to a substrate.
1. A carboxylic acid activating formulation, comprising: a carboxylic acid activating compound, wherein said compound is 1-(3-(diethylamino)-propyl)-4-(2-methoxyphenyl)-1,4-dihydro-5H-tetrazole-5-thione, a coupling molecule and a solvent.
2. A method of attaching a coupling molecule to a substrate, comprising:
obtaining a substrate comprising a plurality of amine groups for linking to a coupling molecule;
contacting said substrate with a carboxylic acid activating formulation comprising: a carboxylic acid activating compound, wherein said compound is 1-(3-(diethylamino)-propyl)-4-(2-methoxyphenyl)-1,4-dihydro-5H-tetrazole-5-thione, a coupling molecule and a solvent;
selectively exposing said formulation to light, thereby activating a carboxylic group of said coupling molecule at a selectively exposed area;
coupling the activated carboxylic group of said coupling molecule to at least one of said plurality of amine groups at said selectively exposed area; and
optionally repeating said method to produce a desired polymer at said at least one carboxylic acid group.
3. The method of claim 2 , wherein said coupling step is performed multiple times at different selectively exposed areas on said substrate.
4. The method of claim 2 , wherein said coupling step has a coupling efficiency of at least 98.5%.
5. The method of claim 2 , wherein said coupling step has a coupling efficiency of at least 90%.
6. The method of claim 2 , wherein said coupling molecule is an amino acid.
7. The method of claim 6 , wherein said amino acid has a protecting group attached to an amine group.
8. The method of claim 7 , wherein said protecting group is Fmoc.