It has long been the goal of molecular biologists to develop a technology that can quantify, in a reliable and reproducible manner, the expression level of every individual protein in a tissue sample. DNA microarrays have been used extensively for the analysis of RNA in cellular extracts, from which the expression of individual proteins can be inferred by assessing the levels of their corresponding mRNAs [11,12,13] (see [14] for a review). Changes at the mRNA level, however, are not necessarily proportional to changes at the protein level because of differences in rates of protein translation and degradation. Furthermore, nucleotide screens are unable to provide information on the post-translational modifications of a protein, which may be critical for a protein's function. After all, it is the protein and not the mRNA that provides cellular function, whether it be for communication, metabolism or building cellular architecture.

Although two-dimensional pulse-field gel electrophoresis (2D PFGE) can be used to analyze the proteins expressed in different cellular extracts directly, it requires both a high degree of technical skill and sophisticated computational analysis to identify protein spots that are present on the gel or blot from one extract but not on the other. Even then, it is still necessary to determine the identity of the corresponding protein. The Holy Grail for such proteomic analyses is a highly sensitive protein array screen, in which the strength of the signal at each point on the array provides a readout of the expression level of each protein in the human body. The paper by Haab, Dunham and Brown in this issue of Genome Biology [15] indicates that such a screen may be close at hand.

The Brown group was among the pioneers of DNA microarrays [11,16], developing many of the robotic systems and protocols that are currently used for screening at the nucleic-acid level [17]. They have now applied the same techniques to the creation and screening of protein microarrays, consisting of either spotted antibodies or spotted protein antigens [15] (see Figure Figure1).1). As each of the antibody-antigen pairs is mutually exclusive - that is, each antibody only binds to a single cognate antigen and vice versa (a feature that makes antibodies particularly well suited to the task of protein profiling) - a single microarray comprising 115 antibodies can be used to assay the presence of different target antigens in a complex mixture. Although the concept of using antibody arrays to profile protein expression is not new, the screen described by Haab et al. [15] achieves, for the first time, the kind of sensitivity and reproducibility that would be required to detect the vast majority of proteins present in a human cell lysate. Furthermore, the protocol is centered on well-established technology that could easily be reproduced by any researcher well versed in the art of DNA arrays. Indeed, the same glass slides, robotic gridders, dye labels, slide readers and image analysis software have simply been adapted for use with proteins rather than with DNA.

Over the past three years there has been considerable excitement about the impending availability of protein arrays, yet remarkably few publications to justify it [18,19]. Of course, protein is quite different from DNA. Whereas the immobilization of DNA to a solid support requires a simple charge interaction, a protein must be attached in such a way as to maintain its folded (and thereby functional) conformation. Although the nucleotide sequence of one piece of DNA differs from the next, they generally have similar chemical and physical properties. Two proteins, on the other hand, may be quite dissimilar, having different sizes, charges, stabilities and solvent solubilities. The binding of one protein to another is an even more complicated affair. The strength of the interaction between a single strand of DNA and its complementary strand is mainly dictated by the length of contiguous base pairing, which on a DNA array can be controlled by laying down different oligonucleotides of the same length. Each interaction that occurs on the surface of a DNA array therefore has a similar (high) affinity. By contrast, different protein-protein interactions may have affinities ranging from femtomolar to micromolar - 12 orders of magnitude difference.

Finally, a truly high-throughput array requires a wide range of binding molecules, each of which has a unique specificity for a given target present in the cell lysate. For DNA arrays, oligonucleotides can be synthesized that correspond to specific nucleotide sequences known to be present at the RNA level. For each protein in the lysate, however, a cognate binder must be first isolated and then tested to confirm its contextual specificity. Thus, if a human cell lysate is to be probed, each binder in the array must specifically recognize a single protein in that lysate and not cross-react with any others. This is where antibodies come into their own. Highly specific monoclonal antibodies can be generated either in vivo by mouse immunization [20] or in vitro using techniques such as phage display [21,22]. Ideally, the antibodies are coupled or adsorbed to a solid support and then probed with a labeled lysate. Several model systems have demonstrated the feasibility of this approach using a handful of antibodies [23,24,25,26]. The publication by Haab et al. [15] takes these experiments one step further, using over a hundred different rodent monoclonal antibodies to simultaneously assay the levels of their respective cognate proteins in a complex antigen mixture.