Protein micro- and macroarrays: digitizing the proteome

• Published in: Journal of Chromatography B Vol. 787; no. 1; pp. 19 - 27
• Main Authors: Lopez, Mary F., Pluskal, Malcolm G.
• Format: Book Review Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 05.04.2003
• Subjects: Protein Array Analysis; Proteins; Proteome; Proteomes; Proteins; MS, mass spectrometry; MALDI TOF, matrix assisted laser desorption/ionization time of flight; Reviews; Microassays; IPG, immobilized pH gradient; LC ms/ms, tandem mass spectrometry; mass spec, mass spectrometry; Macroassays; Proteomes; IEF, isoelectric focusing; 2-D, two-dimensional electrophoresis
• ISSN: 1570-0232; 1873-376X
• DOI: 10.1016/S1570-0232(02)00336-7

The early applications of microarrays and detection technologies have been centered on DNA-based applications. The application of array technologies to proteomics is now occurring at a rapid rate. Numerous researchers have begun to develop technologies for the creation of microarrays of protein-based screening tools. The stability of antibody molecules when bound to surfaces has made antibody arrays a starting point for proteomic microarray technology. To minimize disadvantages due to size and availability, some researchers have instead opted for antibody fragments, antibody mimics or phage display technology to create libraries for protein chips. Even further removed from antibodies are libraries of aptamers, which are single-stranded oligonucleotides that express high affinity for protein molecules. A variation on the theme of protein chips arrayed with antibody mimics or other protein capture ligand is that of affinity MS where the protein chips are directly placed in a mass spectrometer for detection. Other approaches include the creation of intact protein microarrays directly on glass slides or chips. Although many of the proteins may likely be denatured, successful screening has been demonstrated. The investigation of protein–protein interactions has formed the basis of a technique called yeast two-hybrid. In this method, yeast “bait” proteins can be probed with other yeast “prey” proteins fused to DNA binding domains. Although the current interpretation of protein arrays emphasizes microarray grids of proteins or ligands on glass slides or chips, 2-D gels are technically macroarrays of authentic proteins. In an innovative departure from the traditional concept of protein chips, some researchers are implementing microfluidic printing of arrayed chemistries on individual protein spots blotted onto membranes. Other researchers are using in-jet printing technology to create protein microarrays on chips. The rapid growth of proteomics and the active climate for new technology is driving a new generation of companies and academic efforts that are developing novel protein microarray techniques for the future.