The first attempts to analyse the proteome occurred in the early 1970s, making use of a new technique known as polyacrylamide gel electrophoresis (PAGE) (47). Since then, there have been a number of developments in proteomic techniques and a significant increase in their utility. In this review, we provide a brief overview of the most commonly used proteomic approaches.

Gel-based methods belong to the most established techniques in proteomics and remain the preferred choice for separation and semi-quantitative identification of various proteins. The most commonly used method is one-dimensional (1D)-PAGE, which may be used to separate denatured protein samples according to their molecular weight in a polyacrylamide gel (47). Although this technique is used for western blot analyses in numerous laboratories, it has limitations with regards to identification of single proteins within large protein mixtures. Proteins of the same mass are detected at the same position in the gel, leading to a mixed signal.

This problem may be overcome by using two-dimensional (2D)-PAGE. With this method, the proteins are separated by their isoelectric point along a pH gradient in the first dimension, a process termed isoelectric focusing (48). This is followed by separation according to molecular mass. Due to the introduction of the second dimension, separation of ≤10,000 proteins is possible (49). Furthermore, recent developments in protein staining techniques, such as the introduction of fluorescent dyes, have allowed not only a sensitivity of detection in the femtomolar range, but also widened the linear dynamic range by approximately three orders of magnitude (50–55). However, direct comparison between different protein samples has always been a weak point, as separate gels must be run for each sample and methodical errors may intervene with the obtained results. This has been overcome by introducing fluorescence 2D difference gel electrophoresis (2D-DIGE), which allows comparison of ≤3 protein samples in one gel (56,57). In this approach, the respective protein mixes are labelled with cyanine dyes (CyDyes), which bind covalently to the e-amino group of the lysine residues of the proteins. Currently, three different CyDyes are available, namely, Cy2, Cy3 and Cy5, which may be separately detected (57). Specific software, e.g., DeCyder, has been developed to help analyse the gel images. Although this technique is highly sensitive, its power is limited due to potential inconsistent labelling of proteins (56). Furthermore, 2D-DIGE does not overcome the limitations of 2D-PAGE, as all the proteins must be in a molecular weight range between 5 and 150 kDa and a pH range of 3.5–10 in order to be detected (56,58). Proteins that are successfully separated by 2D- or 1D-PAGE, may be further defined by mass spectrometry (MS).

Over the last three decades, developments in liquid chromatography (LC), MS and protein labelling, e.g., the introduction of electrospray ionisation (ESI) and stable isotope labelling by amino acids in cell culture (SILAC), have enabled the establishment of shotgun proteomics. MS is currently commonly used for accurate peptide identification and quantification. Quantitative proteomics strategies rely on relative quantification, comparing the levels of individual peptides identified from one or more experimental samples to those levels from an untreated control sample. This provides an invaluable and powerful tool for global analysis of protein composition; however, it is important to highlight that the proteomic coverage of the genome remains a major technical challenge, as only ~10% of the proteins present in the sample are identified and even fewer are quantified (59). MS-based proteomic approaches may be used to identify and quantify proteins from a whole-cell lysate, an isolated organelle/region of a cell population (e.g., nuclear envelope), or a particular tissue or organism. As previously alluded to, further protein purification may be achieved by means of LC or gel electrophoresis. These strategies allow the removal of high-abundance proteins, which would otherwise mask low-abundance proteins, while also reducing sample complexity for increased peptide identification and quantification. Following purification, equal amounts of protein from each of the samples are proteolytically digested into peptides, often using trypsin. The digested peptides are separated and ionized by LC coupled to ESI and are then subjected to tandem MS (MS/MS). The fractions undergo a first round of MS (MS1), in which the mass-to-charge ratio (m/z) of all ionised peptides is measured, generating a precursor ion spectrum. The relative intensity of each spectrum peak correlates proportionally to peptide concentration, allowing relative quantification across different experimental conditions. Individual peptide populations are then selected for collision-induced dissociation (CID) with an inert gas and a second round of MS (MS2) determines the m/z of the peptide fragments generating a CID spectrum. This spectrum is then compared with a theoretical database produced via an in silico digest for peptide identification (Fig. 1) (60,61). The majority of global proteomic analyses across different experimental conditions are currently performed using stable isotope labelling, mass tag labelling or label-free approaches (62).

SILAC, as first described by Ong et al (63), is an in vivo metabolic labelling technique, enabling the incorporation of different atomic isotopes into proteins as they are being synthesised in the living cell. SILAC is routinely performed using cell culture systems, but it has also been applied to simple organisms (e.g., C. elegans or Drosophila melanogaster) (64) and even mice (65). Stable (non-radioactive) naturally occurring isotopes are variants of a specific chemical element (commonly H, C, N and O), which contain the same number of protons but different numbers of neutrons in each atomic nucleus. Isotopes have identical chemical properties, reducing the risk of introducing experimental bias between differently labelled samples, but the isotopes have different masses; therefore, they are easily identified by MS. The cells are cultured in growth medium with specifically labelled amino acids containing either a light isotope (e.g., ¹²C-lysine and/or ¹²C-arginine) or a heavy isotope (e.g., ¹³C-lysine and/or ¹³C-arginine). ¹³C has an extra neutron compared to ¹²C, which gives ¹³C an increment in its mass number of 1 Da. The substitution of light ¹²C-arginine with heavy ¹³C-arginine results in a 6-Da increment in the mass spectrum of a peptide containing one arginine, as a single arginine residue contains six carbons. Trypsin cleaves lysine and arginine residues at the C-terminus; therefore, using these particular labelled amino acids ensures that all tryptic peptides (except for the C-terminal peptide) contain at least one labelled residue. For SILAC to work effectively, the cells must be grown in labelled growth medium for a number of passages in order to incorporate isotopes into the majority of the proteins. A very high rate of isotopic incorporation (>90%) is achieved in cells after 6–8 doublings (63). At this point, cells that have been differentially labelled undergo the desired treatment, for example, a viral infection. SILAC allows for a maximum of three different samples in a single mass spec run with the use of light (e.g., ¹²C-arginine and ¹²C-lysine; R0K0), medium (e.g., ¹³C-lysine and 2D lysine; R6K4) and heavy (e.g., ¹³C ¹⁵N-arginine and ¹³C ¹⁵N lysine; R10K8) isotope-containing media. A major advantage of SILAC is that, once generated, labelled and unlabelled samples are mixed in equal amounts into one pooled sample. This allows all the samples to be processed together, reducing the risk of external experimental error. Furthermore, due to its accuracy, SILAC is particularly suitable for revealing relatively small changes in protein levels or post-translational modifications. A limitation of SILAC, however, is that certain cell lines may convert excess arginine into proline and, therefore, titration of arginine into the medium may be required (66). In addition, SILAC may not be applicable to cells that are sensitive to changes in the medium composition. Combining SILAC with subcellular fractionation may further reduce sample complexity (Fig. 2).

ICAT was the first method involving the addition of isotopic tags to proteins for quantitative MS. This method was reported in 1999 by Gygi et al (67) and allows labelling of proteins present in any protein sample, including extracts from tissues or body fluids. As opposed to SILAC, labelling occurs in vitro following cell lysis. ICAT relies on the use of a reagent composed of three elements: a biotin molecule to enable purification of the labelled peptides with the use of avidin or streptavidin affinity chromatography; a linker group, which contains stable isotopes (light or heavy); and a reactive iodoacetyl group, which specifically reacts with free thiols on cysteine residues. Following labelling, light and heavy samples are combined into one sample, which is subjected to proteolytic digestion, affinity purification and LC-MS/MS. As labelling only occurs in proteins containing cysteine, which is a rare amino acid, ICAT inherently implies a considerable bias against proteins that lack or contain few cysteine residues; however, for the same reason, this technique is also advantageous when one wishes to reduce complexity in the protein mixture. A modification of ICAT has been devised to overcome this limitation, known as isotope-coded protein labelling (68), in which all free amino groups on intact proteins are isotopically labelled with either light or heavy tags, resulting in a higher proteomic coverage compared to ICAT.

Further techniques using tags of the same mass have also been developed for use in MS-based quantitative proteomics, most commonly known as iTRAQ and TMT. These techniques enable examination of four, six or even eight different experimental conditions in a single MS experiment with the use of up to eight different isobaric mass tags. These tags are all of the same mass and consist of three components: an N-hydroxysuccinimide ester group, which reacts with primary amino groups; a mass tag (reporter) group; and a balance (carbonyl) group. The reporter group is based on N-methylpiperazine and contains a unique number of heavy ¹³C and ¹⁵N substitutions. The masses added by each tag are compensated with balance groups of variable masses to make all tags equal in mass, meaning that the same protein from different samples will behave in the same manner during LC and MS1. Each experimental condition is enzymatically digested individually, the peptides are then tagged and the samples are pooled for LC-MS/MS analysis. Upon collision-induced dissociation, the mass tags are cleaved from the balance groups. During MS2, the intensity of the different tags are used for relative peptide quantification, whereas the peptide fragment ions are sequenced to determine protein identity. As isotopic labelling occurs after enzymatic digestion, the sample complexity is increased and more abundant proteins are overrepresented during MS identification (69). iTRAQ and TMT may also be used for absolute quantification, in which the exact amount of a protein can be measured. The differences between these isobaric mass tags and the previously mentioned isotope-coded affinity tags are shown in Fig. 3.

As the labelling of proteins is always limited by various factors, two label-free techniques have recently been developed for use in quantitative proteomics.

Spectral counting is simply based on counting mass spectra collected during a tandem MS run, as previous studies demonstrated that the number of these mass spectra is proportional to the concentration of a given peptide and, therefore, its respective protein in the sample (58,70). Prior to ionisation and MS/MS, the peptides resulting from the initial protein trypsinisation are separated by LC. Elution of highly concentrated peptides into the MS/MS ionisation chamber occurs over a longer period compared to the elution of peptides with lower concentrations; therefore, more spectra of the more concentrated peptides may be acquired compared to the less concentrated peptides (70). Although modern LC systems are capable of very accurate separation, there is always the possibility of co-eluting peptides when analysing complex protein samples (58). This has resulted in critical discussion regarding this label-free method, particularly as no other physicochemical properties of the individual peptides are measured (71). However, there have been recent developments to improve spectral counting and moving from relative quantification to absolute protein measurement. The normalised spectral abundance factor (NSAF), the distributed NSAF and the normalised spectral index take into account not only the number of spectra, but also peptide count, protein length, sample-to-sample variation for replicate analyses, fragment-ion intensity and the distribution of spectral counts of peptides shared by different proteins (72–74). The absolute protein expression aims for absolute protein measurement by calculating the proportionality of expected peptides after trypsinisation and the observed peptides for a given protein after MS/MS (75).

Measurement of chromatographic peak areas (or MS signal intensities) is the second method used for label-free quantitative proteomics. The peptides are separated by LC according to their physical properties, e.g., charge or hydrophobicity, followed by ionisation and detection of peptide precursor ions in a mass spectrometer. Every precursor ion generates a specific mono-isotopic peak, the intensity of which may be shown as function of the LC retention time in an extracted ion chromatogram. The chromatographic peak areas for each peptide, determined by the area under the curve, correlate with the abundance of the respective peptide. Therefore, a relative quantification between different protein samples is possible (76–78). However, this requires a high level of reproducibility between the different samples (71,78). Moreover, due to identifying and focusing on specific precursor ions at an early stage, there may be a reduction in the peptides sequenced during MS/MS (79). To overcome this, two separate analyses, one LC-MS and one LC-MS/MS, may be performed for each sample. Nevertheless, newer and faster mass spectrometers are able to collect data for MS as well as MS/MS scans at a satisfying rate (71,79).

Although label-free is currently the least accurate proteomic method, it is worth considering, as it displays distinct advantages. First, the money- and time-consuming step of introducing labels into proteins is not necessary, which also leads to a reduction in experimental stages. Furthermore, although multiplexing is not available for label-free samples, there is no limit for parallel experiments if all the stages of sample preparation and analyses are reproducible. Finally, label-free quantifications exhibit a higher dynamic range compared to stable isotope labelling. The merits of spectral counting, in particular, have been demonstrated when seeking large changes in protein levels compared to SILAC-labelled samples (70,71,80).

There are several factors to be considered when selecting a particular method (Fig. 4), but often different approaches yield comparable results; therefore, most consideration should potentially be given to the ease of application and how well equipped a lab is to attempt any given approach.

Proteomic methodologies have been demonstrated to be useful in a wide range of biological investigations, including numerous studies of interactions between virus and host proteomes. There are a number of examples of γ-herpesvirus studies that have utilised these approaches, which have helped elucidate several aspects of their biology.

Early analyses of viral proteomes often focus on the composition of the mature viral particle, as the proteins found within are often instrumental to a successful infection. As with all herpesviruses, EBV and KSHV have complex virions, constructed of an inner nucleoprotein core, a viral capsid, an inner tegument layer and a lipid envelope (81). Surprisingly, despite being the first true human oncovirus to be discovered, only a single study has used proteomic analyses to comprehensively study EBV virion composition (82). In that study, the EBV lytic cycle was induced from latently infected B cells by the ectopic expression of the EBV lytic switch protein, Zta. Mature virus particles were purified using density gradients, de-enveloped and subjected to in-gel trypsin digestion and LC-MS/MS. This analysis largely demonstrated that EBV virion morphogenesis follows that of other herpesviruses, such as the model herpesvirus, herpes simplex virus (HSV). ICAT was also used to determine how likely a protein was to be associated with the envelope or the EBV capsid. In this example, ¹²C ‘light’ labelled enveloped virions were mixed with ¹³C ‘heavy’ labelled virions that had been treated with detergent to remove the envelope. Following normalisation between samples on the major capsid protein, it was observed that several cellular proteins were major components of mature EBV virions, including β-actin (one of the most abundant tegument proteins), cofilin, tubulin, heat shock protein (Hsp)70, Hsp90 and other actin-associated proteins (ARPs), such as profilin, ezrin, radixin, moesin and α-actinin. Hsp70, α-tubulin, β-tubulin and actin were shown to be tightly associated with capsids, suggesting that they may be involved in stabilising the capsids or that they may be required immediately after de-envelopment during de novo infections. Additional functions for the cellular proteins may include EBV virion morphogenesis and egress.

Initial determinations of the KSHV virion components were performed in a similar manner, subjecting mature virions purified by density gradient to 1D-gel electrophoresis, in-gel tryptic digest and MS (83). In total, 24 proteins of structural, regulatory and signalling roles were identified, including 5 capsid proteins, 8 tegument proteins, 8 glycoproteins found within the lipid envelope and a further 3 proteins associated with the virion. Of note, several of the identified proteins were of cellular origin, including a number of proteins also found in EBV virions, such as β-actin and the ARPs ezrin and moesin. The roles of these proteins in the viral particle have not yet been elucidated; however, their presence suggests that they are required for virion stability or during the early stages of infection.

The chaperones Hsp90 and Hsc70, identified in the virions of a wide range of viral families, were also identified in the tegument of KSHV. These proteins have been shown to play numerous roles in viral processes, ranging from relocalization of key viral factors to aiding in the reverse transcription of retroviral genomes. Furthermore, the KSHV lytic reactivator protein replication and transcription activator (RTA) (84) was identified as a component of the KSHV tegument, suggesting that RTA drives a round of lytic gene expression immediately after infection. These studies demonstrated the efficacy of using reduced-complexity samples with MS-based proteomics to identify a subset of viral and cellular proteins involved in different aspects of viral biology.

In an attempt to gain understanding of EBV pathogenesis, Alsayed et al (85) performed a proteomic analysis of PTLD tissues from solid organ transplant patients using a protein microarray technique. The proteins that were dysregulated included proteins of the phosphoinositide 3-kinase (PI3K)/mammalian target of rapamycin, nuclear factor-κB and Hsp90 pathways, all of which are entirely consistent with the latency III gene expression profile in PTLD. Interestingly, when specific inhibitors of these proteins were then tested in EBV⁺ and EBV^- cell lines, they were found to be specifically cytotoxic in the EBV⁺ lines. Indeed, it was recently demonstrated that the Hsp90 inhibitors geldanamycin, 17-allylamino-17-demethoxygeldanamycin and 17-dimethylaminoethylamino-17-demethoxygeldanamycin specifically decreased EBNA1 translation, leading to cytotoxicity of EBV⁺ cells and significantly inhibiting lymphoproliferative disease in severe combined immunodeficiency mice (86,87). Together, these early results highlighted the value of proteomics in identifying novel therapeutic targets.

Proteomic analyses have also been applied in order to understand how the human γ-herpesviruses manipulate intercellular communication. In addition to the secretion of soluble factors that promote the establishment of latency (or indeed, tumourigenesis), virally infected cells also release modified exosomes. These are a class of endosomal-derived membrane microvesicles from multivesicular bodies that, after release, may fuse with recipient cells, into which they release their contents and modulate biological activities. Although this is a normal physiological process, there is evidence suggesting that altered exosome function may be pathogenic, particularly during malignancy. It was demonstrated that EBV-infected cells release exosomes containing virally-encoded miRNAs and proteins and that these factors are able to alter target cell function (88–90). For example, EBV’s major oncoprotein LMP1 was highly enriched in exosomes secreted from nasopharyngeal carcinoma (NPC) cells and the transfer of these to recipient cells activated several LMP1-associated signalling cascades, including PI3K/AKT and mitogen-activated protein kinase/extracellular signal-regulated kinase (91). LMP1 has also been identified in B-cell-secreted exosomes and this may be important for inducing proliferation and B-cell survival, a crucial step in the establishment of EBV latency and colonisation.

However, there remains the major question whether viral infections dictate the composition of secreted exosomes. This was recently addressed by Meckes et al (92) using a combination of MS and 2D-DIGE to determine the repertoire of proteins in EBV⁺, KSHV⁺ and dually infected cell line exosomes, compared to non-infected counterparts. In that study, a total of 871 proteins were identified from all exosome preparations and 449 of these proteins were common among infected and non-infected cell lines. Therefore, several hundred exosome proteins were enriched as a result of γ-herpesvirus infections. Some of these proteins were specific to EBV (n=93) and others to KSHV (n=22), suggesting that these different viruses manipulate the exosome proteome in diverse ways, possibly in order to optimally promote their particular life cycles. Furthermore, a 2D-DIGE, coupled with a spectral count-based quantitative proteomic approach, was employed to compare the exosomes of LMP1⁺ and LMP1^- cells, confirming that several of the alterations in the EBV-associated exosome cargo were due to LMP1. Moreover, the pathway analysis revealed that both EBV- and KSHV-associated exosome components largely affect similar cellular pathways, although KSHV exosomes were enriched in proteins involved in cellular metabolism, whereas EBV-associated exosomes were geared towards cellular signalling pathways.

The abovementioned findings demonstrate that proteomic-based research is able to identify multiple protein pathways that are altered by related viruses and put these into the context of a viral infection. However, a potential caveat that exists in a majority studies regarding the human γ-herpesviruses is the lack of isogenic virus-negative counterparts to rule out the possibility that some differences are purely cell type-specific. Despite this caveat, however, these studies enhance our understanding of how KSHV and EBV manipulate the tumour microenvironment and provide potential new avenues for therapeutic intervention. Interestingly, several of the proteins identified in mature γ-herpesvirus virions have also been detected in their exosomes (e.g., actin and ezrin), signifying the possibility that virally induced exosomes may mimic viral infection. If this is true, the extent to which it may benefit virus colonisation remains to be determined. The next challenge will be to elucidate how viruses dictate exosome proteomes and how this translates in vivo.

Proteomic approaches have also been used to investigate the function of individual viral proteins. The EBNA2 protein is considered to be the master transcriptional activator, switching on the expression of all of EBV’s immortalising genes, as well as various cellular genes known to be critical for EBV infection, such as CD23. In an attempt to identify proteins altered due to EBNA2 expression, 2D-PAGE was applied to a protein sample from a conditionally immortalised B-cell line, in which EBNA2 is activated by translocation to the nucleus, due to the addition of oestrogen (93). In that study, EBNA2 target proteins and the proteins that were induced during primary B-cell infection were shown to correlate, highlighting the major role of EBNA2 during the establishment of latency and B-cell immortalisation. A total of 20 differentially expressed proteins were identified, 12 of which were upregulated, including the protein synthesis and degradation factors eIF5a, P0, PA28γ and ubiquitin thiolesterase L3, as well as two proteins involved in nucleotide metabolism, Nm23-H1 and pyrophosphatase. Some of the best characterised EBNA2-responsive proteins were not identified, however, suggesting incomplete coverage due to the nature of the proteomic approach employed.

Similarly, the effect of individual KSHV protein expression has been investigated using a gel-based approach. 2D-DIGE was successfully utilised to analyse the protein content of endothelial cells expressing the KSHV vFLIP protein (94). This study identified 14 proteins upregulated upon vFLIP expression, the most highly upregulated of which was manganese superoxide dismutase (MnSOD). Interestingly, this is an antiapoptotic enzyme that has also been shown to be upregulated in KSHV-infected cells. Importantly, previous transcriptome analyses also identified MnSOD to be upregulated at the RNA level, demonstrating the possibility of combining proteomics and transcriptomics approaches to validate and enhance results (94,95) (see Section 4).

Another proteomic-based study of EBV investigated the transformation potential of the EBV LMP1 oncoprotein in NPC cell lines (96). In that study, a total of 250 proteins were detected by iTRAQ-based analysis, 12 of which were shown to be differentially expressed (although proteins that changed as little as 1.33-fold were also considered), including 6 proteins involved in signal transduction: voltage-dependent anion channel 1, S100-A2, hormone-induced protein-70, ubiquitin, tumour protein translationally-controlled 1-like protein and 4F2hc, as well as 3 proteins pertaining to cyctoskeleton formation: keratin-75, TB8 and dynein light chain 1.

The first SILAC-based study designed to investigate a small number of changes in specific subcellular compartments utilised the expression of the KSHV K5 protein (97). Modulation of the host immune response, particularly via major histocompatibility complex (MHC) class I molecules, is a common trait amongst pathogens. The KSHV-encoded K3 and K5 proteins, which function as membrane-bound RING-CH ubiquitin ligases and target MHC I for lysosomal degradation, are homologues of the K3 family of viral immune modulators. Importantly, other viral downregulators of MHC I are also known to target additional transmembrane proteins pertaining to different cellular pathways. In order to identify any novel K5 targets, plasma membrane, endoplasmic reticulum (ER) and Golgi apparatus were isolated from labelled control cells or cells expressing K5. In addition to the expected downregulation of MHC I, 3 novel peptides were found to be downregulated in the plasma membrane of cells expressing K5: activated leukocyte cell adhesion molecule, bone marrow stromal cell antigen 2 (BST-2) and syntaxin-4. The identification of these proteins marked a precedent in SILAC proteomics, as it demonstrated a new approach for identifying additional targets of viral proteins. BST-2 (also known as tetherin) is of particular interest, as this protein was first identified as a host restriction factor that prevents the release of budding retroviruses from the plasma membrane. HIV is able to counteract BST-2 via its auxiliary protein, viral protein unique, by co-opting a cellular ubiquitin ligase, βTrCP, resulting in BST-2 degradation. Subsequent studies confirmed that BST-2 is indeed a bona fide target of K5, although it was shown to be subjected to proteasomal degradation as it left the ER, rather than being degraded at the plasma membrane by the lysosome (as is true of other K5 targets). Therefore, similar to HIV, KSHV has also developed a mechanism of circumventing BST-2 function, although this virus has evolved its own specialised ubiquitin ligase, namely K5.

MS-based proteomics have also been used to identify cellular proteins binding to the terminal repeat regions (TRs) of the KSHV genome during latency. KSHV TRs contain the latent origin of viral replication and play a major role in the maintenance and spread of the viral episome among dividing cells. In order to further characterise these important regulatory elements, TR sequences were used to affinity capture proteins from KSHV-positive cell lysates, which were subjected to MS-based proteomic analysis (98). In total, 123 proteins were found to bind the TRs of KSHV and further analysis on 4 of these proteins, namely ataxia telangiectasia and Rad3-related protein, transcription activator BRG1, nucleophosmin 1 and poly(ADP-ribose) polymerase 1, demonstrated that they associate with the KSHV-encoded LANA. This suggested that proteins binding TR sequences may play a role in viral latency.

Furthermore, by employing affinity capture methods coupled to 1D-PAGE and MS, glutathione S-transferase-tagged N- and C-terminal regions of LANA were used to capture and identify protein interaction partners of LANA (99). Several proteins were found to bind to the N-terminus (n=53) and the C-terminus (n=56) and functional analysis of the protein groups identified 27 different categories, including ATPases, ribonucleoproteins and cytoskeletal proteins. Whilst the majority of these novel interactions are yet to be fully characterised, most of the proteins that bound LANA were found to be transcription factors and DNA-binding proteins, suggesting that LANA plays an important role in transcriptional control.

More recently, our laboratory has undertaken SILAC-based proteomics to elucidate the effects of the essential KSHV mRNA processing protein, ORF57 (100,101), on cellular pathways. To this end, an inducible HEK293-based system expressing ORF57 was utilised. To maximise the data obtained from the study, cellular fractionation was performed to separate the major cellular compartments where ORF57 is known to be present: the cytoplasm, nucleoplasm and nucleoli (102). Predictably, as ORF57 is a known viral RNA processing protein, its expression led to an enrichment of proteins involved in RNA processing, RNA post-transcriptional modification and gene expression, particularly in the nucleolar fraction, where ORF57 is highly abundant (103,104). Importantly, the analysis also identified an enrichment in DNA repair proteins that led to the discovery of a novel role for ORF57 in genome instability (105). That study highlighted the significance of large-scale proteomics studies for identifying novel proteins or cellular pathways of interest. Moreover, cellular fractionation and isolation of cellular compartments or organelles linked to SILAC proteomics will substantially increase the flexibility of this type of approach.

Combining protein immunoprecipitation with mass spec-based quantitative proteomics provides another way to reduce sample complexity and gain greater insight into the intricacies of viral infection. Malik-Soni and Frappier (106) have used this method to elucidate the interaction partners of the EBV EBNA1 protein in EBV-positive and -negative NPC cell lines. In that study, EBNA1 was found to have very similar interactomes in the two different cell backgrounds and these interaction profiles largely agreed with previous studies using HEK 293T cells. Furthermore, the EBNA1 interaction partners in AGS cells infected with latent EBV were highly similar to those in lytically infected cells, demonstrating that several of the EBNA1-host protein interactions occur independent of EBV infection. Of note, EBNA1 was also shown to associate with numerous heterogeneous nuclear ribonucleoproteins and the La protein, which associated with the 3′ ends of newly synthesized small RNAs and had previously been shown to bind EBV EBERs (107). The interaction between La and EBNA1 only occurred in the context of full EBV infection and was ablated by RNase treatment, suggesting this interaction is bridged by EBERs. EBNA1 also appeared to interact with the nucleolar protein B23 (nucleophosmin), a protein that frequently plays a role in infection with other viruses, such as KSHV and HIV-1 (98,108).

Other large-scale studies have also added to our knowledge of the KSHV proteome, although not strictly through a proteomic approach. For example, a large study was performed by Sander et al (109) with the aim to map the subcellular localisation of every KSHV protein in HeLa cells in order to elucidate potential roles of proteins within the context of the viral infection with regard to their location.

Greater understanding of a viral proteome may also be used to create novel diagnostic tools. Recently, a 96-well format multiplex bead-based assay was used to analyse the serological response of 2 groups of individuals previously diagnosed with KSHV-associated malignancies (n=36) or with a low likelihood of KSHV infection (n=43) to 73 different recombinant proteins encompassing most of the KSHV proteome (110). Historically, the KSHV ORF73 and K8.1 proteins have been used to determine whether an individual is infected; however, the patterns of reactivity in those infected with KSHV were found to be highly variable. That study identified 6 more viral proteins that may be tested for to distinguish between KSHV-positive and -negative individuals, providing a more powerful and reliable tool for clinical KSHV serodiagnosis.

This selection of proteomic-based research demonstrates the power of the numerous techniques that have been developed in this field. Combining proteomic techniques with other large-scale systems biology approaches may provide an even greater insight into the various processes occurring within populations.