Substrates, peptide arrays, and methods
Disclosed herein are formulations, substrates, and arrays. Also disclosed herein are methods for manufacturing and using the formulations, substrates, and arrays. Also disclosed are methods for identifying peptide sequences useful for diagnosis and treatment of disorders, and methods for using the peptide sequences for diagnosis and treatment of disorders, e.g., celiac disorder. In certain embodiments, substrates and arrays comprise a porous layer for synthesis and attachment of polymers or biomolecules.
1. An array of features comprising at least 10,000 features, each feature is attached to a surface of the array at a different positionally-defined location, the positionally-defined location of each feature corresponds to a positionally-defined location of a pillar, wherein the top surface of each pillar is at least 1 μm 2 in size, and
wherein each feature comprises a different predetermined peptide chain compared to the other features, each feature comprises at least 500 identical full-length peptide chains, wherein each identical full-length peptide chain has a predetermined full-length of at least 7 amino acids in length, and
the purity of each feature with regards to the fraction of full-length predetermined peptide chains is a fraction F of the full-length predetermined peptide chains of each feature having a predetermined sequence and a predetermined full-length sequence length N being characterized by F=10 (N+1)·log(E/100%) with an average coupling efficiency E of at least 98.5% for coupling each amino acid of the predetermined sequence, and the sequence length N being at least 7 amino acids in length, the fraction of the less than full-length predetermined peptide chains equaling (1-F); and
the surface comprising a substrate, the substrate comprising:
a planar layer having an upper surface and a lower surface, and
a plurality of pillars operatively coupled to the layer in the positionally-defined locations, wherein each pillar has a planar surface extended from the layer, wherein the distance between the surface of each pillar and the upper surface of the layer is between 1,000-5,000 angstroms, and wherein the plurality of pillars are present at a density of greater than 10,000/cm 2 .
2. The array of claim 1 , wherein said surface comprises a porous surface layer, and
said porous layer comprises a plurality of free carboxylic acid groups.
3. The array of claim 2 , wherein said carboxylic acid groups are oriented in multiple directions.
4. The array of claim 2 , wherein said porous layer comprises a plurality of coupling molecules each attached to said array via a carboxylic acid group.
5. The array of claim 2 , wherein said porous layer comprises a plurality of peptide chains each attached to said array via a carboxylic acid group.
6. The array of claim 1 , wherein the features comprise a plurality of distinct, nested, overlapping peptide chains comprising subsequences derived from a source protein having a known sequence.
7. The array of claim 1 , wherein the surface comprises a substrate, the substrate comprising: a first layer, wherein said first layer comprises a plurality of unprotected carboxylic acid side groups.
8. The array of claim 1 , wherein the planar layer comprises a metal.
9. A method of producing an array of features, comprising:
obtaining a substrate comprising a planar layer having an upper surface and a lower surface; and a plurality of pillars operatively coupled to the layer in different positionally-defined locations, wherein each pillar has a planar surface extended from the layer, wherein the distance between the surface of each pillar and the upper surface of the layer is between 1,000-5,000 angstroms, wherein the surface of each pillar is parallel to the upper surface of the layer, and wherein the plurality of pillars are present at a density of greater than 10,000/cm 2 ; and
coupling through a series of coupling reactions the features to the plurality of pillars, each features attached at different positionally-defined locations comprising a plurality of peptide chains, the positionally-defined location of each feature corresponds to a positionally-defined location of a pillar, wherein the top surface of each pillar is at least 1 μm 2 in size, and
wherein each feature comprises a different predetermined peptide chain compared to the other features, each feature comprises at least 500 identical full-length peptide chains, wherein each identical full-length peptide chain has a predetermined full-length of at least 7 amino acids in length, and the purity of each feature with regards to the fraction of full-length predetermined peptide chains is a fraction F of the full-length predetermined peptide chains of each feature having a predetermined sequence and a predetermined full-length sequence length N being characterized by F=10 (N+1)·log(E/100%) with an average coupling efficiency E of at least 98.5% for coupling each amino acid of the predetermined sequence, and the sequence length N being at least 7 amino acids in length, the fraction of the less than full-length predetermined peptide chains equaling (1-F); and wherein the array comprises at least unique 10,000 features.
10. The method of claim 9 , wherein the features are coupled to the pillars using a coupling formulation, comprising a solvent, a water soluble polymer, a water soluble coupling molecule, a water soluble neutralization reagent, and a water soluble coupling reagent.