Identification of protein binding sites

Abstract

The disclosure relates to the field of molecular recognition or detection of discontinuous or conformational binding sites or epitopes corresponding to a binding molecule, in particular, in relation to protein-protein, protein-nucleic acid, nucleic acid-nucleic acid or biomolecule-ligand interactions. Provided is a synthetic molecular library allowing testing for, identification, characterization, or detection of a discontinuous binding site able to interact with a binding molecule, the library having been provided with a plurality of test entities, each test entity comprising at least one first segment spotted next to a second segment, each segment having the capacity of being a potential single part of a discontinuous binding site.

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of co-pending application Ser. No. 10 / 411,869, filed on Apr. 10, 2003, now U.S. Pat. No. ______, which is a continuation of International Application PCT / NL01 / 00744, filed Oct. 10, 2001, designating the United States, published in English Apr. 18, 2002, as WO 02 / 31510 A1, which claims priority from EP 00203518.6 filed Oct. 11, 2000, the contents of each of which are incorporated herein by this reference.FIELD OF THE INVENTION[0002]The invention relates to the field of molecular recognition or detection of discontinuous or conformational binding sites or epitopes corresponding to or interacting with a binding molecule, in particular, in relation to protein-protein or protein-ligand interactions.BACKGROUND OF THE INVENTION[0003]Interactions between binding molecules, which in general are biomolecules and their corresponding ligands, are central to life. Cells often bear or contain receptor molecules that i...

AI Technical Summary

Benefits of technology

[0028]Highly diverse binding body libraries can be generated based on systematic combination of relatively small numbers of random peptide segments. A library of 100 binding bodies is easily produced using positionally defined peptide segment arrays as described herein. Screening of such a library with any given molecule is simple, fast and straightforward. Hits can be translated directly into the amino acid or segment make up of the binding body due to the positionally defined array. A library of 10,000 binding bodies can be easily generated by combining all peptides from smaller libraries with each other or by starting with a larger solid support surface. A library of 1,000,000 binding bodies can, for example, be easily generated by combining all peptides of smaller libraries into binding bodies that contain three segments. Thus, a large diversity of binding bodies can be generated starting with relatively small numbers of random peptides (for instance, 10) and multiple combinations of peptides combined into a single binding body (for instance, 6) to arrive at a diversity of 1,000,000 or even larger.

[0054]A preferred embodiment of the invention further allows up-scaling of the synthesis concerning the number of constructs on, for example, a solid support per square centimeter. To facilitate generation of a great many possible constructs, containing, for example, test entities (pairs, threesomes or larger pluralities) comprising at least two peptide segments of a protein, many thousands of peptide constructs are made. For instance, when all constructs in which both segments are, for instance, twelve amino acids long are derived from a small protein with a length of 100 amino acid residues are needed, already 89×89=7,921 peptide constructs are made if the segments are only linked to the solid phase, for instance, via the C-terminus for the first segment and the N-terminus of the second segment, or visa versa, or both, using only one type of link. For a protein with a length of 1,000 amino acid residues, at least 989×989=978,121 constructs are made. For efficient ELISA testing of these numbers of constructs, high construct densities on the solid support are preferred. High densities of constructs on a solid support are provided by the invention, wherein, for instance, (a layer of) a first segment with a bromoacetamide group at the N-terminus is synthesized on a surface of, for instance, 1 cm2. On yet another part of the surface, another first-segment may be applied. On each of such a peptide-functionalized surface of the support, a set of, for instance, 10, preferably 50, preferably 100, or more second, peptide segments containing a free thiol group are spotted or gridded in a positionally or spatially addressable way, giving, after coupling, so many different peptide pairs. Spotting can, for instance, be done using piezo drop-on-demand technology, or by using miniature solenoid valves. Gridding can, for instance, be done using a set of individual needles that pick up sub-microliter amounts of segment solution from a microtiter plate containing solutions comprising the second segments. After the linking reaction, subsequent deprotection and extensive washing of the support to remove uncoupled peptide gives at least a peptide construct pair density as large as 10 to 50, or even 100 to 200, or up to 50 to 1000 spotted pairs per square centimeter. This density allows the screening of a great many possible peptide pairs or binding bodies derived from the proteins for binding with an antibody. For example: in a preferred embodiment 20,000 to 100,000 constructs are made on 1000 cm2. Typically, the surface is then screened for binding in ELISA with 100 ml of antibody solution containing 1-10 μg of antibody / ml. For example, indirect or direct fluorescence detection allocates antibody binding constructs. Direct fluorescence detection with confocal scanning detection methods, for example, allows antibody detection on spots generated with droplets of peptide-solution in the sub-nanoliter range, making even higher construct densities feasible. Of course, nucleic acid libraries can be made in a similar fashion.

Problems solved by technology

However, with existing libraries, no attention is given to synthesizing specific segments in close proximity to each other so that they together can represent a putative binding site.

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