- Research article
- Open Access
Evidence for the adaptation of protein pH-dependence to subcellular pH
BMC Biology volume 7, Article number: 69 (2009)
The availability of genome sequences, and inferred protein coding genes, has led to several proteome-wide studies of isoelectric points. Generally, isoelectric points are distributed following variations on a biomodal theme that originates from the predominant acid and base amino acid sidechain pKas. The relative populations of the peaks in such distributions may correlate with environment, either for a whole organism or for subcellular compartments. There is also a tendency for isoelectric points averaged over a subcellular location to not coincide with the local pH, which could be related to solubility. We now calculate the correlation of other pH-dependent properties, calculated from 3D structure, with subcellular pH.
For proteins with known structure and subcellular annotation, the predicted pH at which a protein is most stable, averaged over a location, gives a significantly better correlation with subcellular pH than does isoelectric point. This observation relates to the cumulative properties of proteins, since maximal stability for individual proteins follows the bimodal isoelectric point distribution. Histidine residue location underlies the correlation, a conclusion that is tested against a background of proteins randomised with respect to this feature, and for which the observed correlation drops substantially.
There exists a constraint on protein pH-dependence, in relation to the local pH, that is manifested in the pKa distribution of histidine sub-proteomes. This is discussed in terms of protein stability, pH homeostasis, and fluctuations in proton concentration.
The post-genomic era allows many basic questions to be addressed, such as the nature of the biological components , control of expression levels for these components , their interaction networks and dynamics , and the ultimate realisation of metabolic function from the parts . Even for proteins, the most studied nodes of biological interaction and function, there is much to discover about how form relates to function. Differences in the characteristics of amino acid sidechains, and in the stoichiometry of their incorporation into proteins, means that physico-chemical properties of proteomes and sub-proteomes can be variable. Several reports of proteome-wide properties have appeared. Features studied include amyloidogenic potential and biological context , propensity for disorder and protein degradation , amino acid composition and gene expression , protein targeting and N-terminal features , and the inclusion of physico-chemical properties into proteome browser resources .
Protein isoelectric point (pI) can be conveniently estimated from amino acid sequence. Three-dimensional structure gives rise to charge interactions that are important in considering protein folded state stability, but generally give small changes in pI compared with linear sequence . Several groups have looked at computed proteome-wide pI distributions, with the outcomes falling into two overall categories. First, there has been discussion of the form of the pI distribution with pH [11–13], and demonstration that a general bimodality results from the predominant acidic and basic pKas of the Asp/Glu and Lys/Arg sidechains. Second, the relative populations of peaks (acidity versus basicity, or pI bias) has been studied with respect to organism environment and taxonomy, and subcellular location. It has been proposed that average pI correlates with growth temperature for orthologues , and with bacterial growth conditions , that pI bias correlates with taxonomy , and that pI distribution varies according to compartmentalisation within the Arabidopsis chloroplast . Other work indicates that, for the most part, pI distributions are not correlated with subcellular location or taxonomy . Amongst these varying conclusions, observations reinforced by multiple reports are that: individual protein pIs tend towards less extreme values for longer sequences, as a result of sampling statistics of acidic/basic amino acids [16, 19]; subcellular proteome pIs may give net charge at environmental pH to mitigate against protein aggregation [18, 20]; smaller proteomes tend to be more basic [15, 16]. This last trend is particularly evident for the small proteomes of intracellular parasites, and does not appear to be fully explicable in terms of genome AT bias. Processes suggested to underlie the trend include adaptation to environmental constraints, such as elevated host pH , and differences in the rate of accumulation of mutations (higher in intracellular organisms than free-living ones) .
3D structures are known for many proteins, and may be modelled for many more . Structure can be used to predict physico-chemical properties, which in turn can aid understanding of function or environmental adaptation, for example comparing proteins from mesophiles and extremophiles  or distinguishing Enzyme Commission classes for enzymes . Charges contribute to protein stability, evident from simple geometric analysis . The role of ionisable groups has been studied extensively, with regard to both protein stability and solubility , and in terms of specific functionality, such as proton buffering by hemoglobin . Computational models of charge interactions  can be applied across databases, looking for example at predicted ionisations of amino acids . Varying degrees of model complexity have been introduced, and are assessed through agreement with experiment for properties such as pKas, the pH-dependence of folding energy, and mutational effects. We have found that a relatively simply model for charge interactions captures the properties of surface ionisable groups , whereas more detailed accounting of a protein/water interface is required for substantially buried groups . Since the great majority of ionisable groups lie at the surface, the simplified method is appropriate for application to wide-scale structural proteomics, so long as detailed questions are not asked of the more buried, typically catalytic site, ionisable groups. This has been shown in a previous study, where we focussed on comparing isoelectric points predicted from sequence and structure . It was found that predicted pI, averaged over the protein structures in a subcellular compartment, tends to lie away from the subcellular pH, consistent with a role in mitigating against isoelectric point aggregation. The subcellular average of the pH at which proteins are predicted to be most stable appeared to be a closer match to subcellular pH, than was the average pI. This preliminary observation, which is consistent with other computational work finding that the predicted pH of maximal stability can be quite different to the pI , is now investigated in detail. We find that the (pH-dependent) maximum in protein stabilisation relates to modulation of histidine pKas by 3D interactions. These residues are largely at the surface and not recognised individually to be of primary functional importance, and yet their cumulative properties associate with subcellular pH. We discuss the physiological context for this result, including pH homeostasis, pH sensing and stochastic effects.
Results and Discussion
pH-dependence of stability and subcellular pH
A dataset of protein structures annotated by subcellular location was constructed as described in the Methods section (Figure 1). Figure 2 illustrates the major ionisation regions for proteins on a schematic plot of the pH-dependence of folding energy (ΔGFU, the difference between the folded (F), and unfolded (U), states). Acidic and basic titrations underpin the generally bimodal pI distributions observed for proteins , since the numbers of (Asp + Glu) with acidic pKas, or (Lys + Arg) with basic pKas, normally exceed the number of His, which ionise in the central pH range. While the balance of (Asp + Glu) and (Lys + Arg) mostly determines pI, it follows from the proportionality between ∂ΔGFU/∂pH and ΔQFU (the difference in net charge between folded and unfolded forms) , that the pH-dependence of stability in the central pH range is determined largely by histidine ionisation (Figure 2). Further, this slope (although small when histidine content is low) is generally negative or positive according to whether the protonated state of histidine is stabilised (ΔQFU positive) or destabilised (ΔQFU negative) in the folded protein. This in turn determines whether the pH value at minimal ΔGFU (pH [ΔGFU(min)], Figure 2) is towards the acidic or basic titration block, again yielding a generally bimodal distribution.
Isoelectric and pH-dependent properties were calculated and examined for correlation with each other and with the measured environmental pH values (Table 1). The average across each subcellular compartment of the pH at minimal ΔGFU, denoted <pH [ΔGFU(min)]> correlates better with subcellular pH than do the analogous averages for pI, <pI(F)> and <pI(U)> (see also Figure 3), although none of these properties matches subcellular pH across the entire range. Table 1 also shows the correlations when calculations are repeated with histidine ionisations removed. Here, only average isoelectric properties and subcellular pH are correlated, demonstrating that histidine ionisation lies behind the correlation of <pH [ΔGFU(min)]> with subcellular pH (Figure 2). Further, histidine location rather than composition is implicated, since neither subcellular pH nor <pH [ΔGFU(min)]> correlate with the subcellular averaged ratio of histidine to other charged amino acids, <His/(Acid+Base)> (Table 1). The nature of pH [ΔGFU(min)] versus His/(Acid+Base) for individual proteins (not shown) is that more acidic or basic pH [ΔGFU(min)] map to higher His/(Acid+Base), while lower His content maps to a relatively underpopulated central zone of pH [ΔGFU(min)], bearing out the schematic indications of Figure 2.
Histidine pKas and subcellular location
Histidine pKa deviations from the model compound value, obtained in the pH-dependence calculation and averaged for each protein, correlate well with <pH [ΔGFU(min)]> (R2 = 0.99, not shown). In Figure 4(a), histidine pKa deviations are plotted against subcellular pH, again with good correlation. These are now averaged per histidine, <Δ pKa [His]>, since the protein-specific condition implicit in pH [ΔGFU(min)] is lost. Figure 4(b) shows compartment-specific <ΔpKa [His]> with the ranges observed, using the 5% and 95% ranked ΔpKa [His] values within each location. Variation across the subcellular averages is much smaller than the variation of histidine ΔpKas. We have investigated previously whether calculations of <pH [ΔGFU(min)]> change substantially upon the inclusion of more a detailed charge interaction scheme, or a model for residual charge interactions in the unfolded state . Although pKas can be perturbed in the U form [34, 29], it was found that the effect of these modelling adjustments on <pH [ΔGFU(min)]> was small . Furthermore, in the current work, we looked at a sequence-based U form model for charge interactions, with nearest neighbour pairs dominating. If this were to yield correlations with subcellular pH, then the analysis would not be restricted to protein structures. However, the U form model proved too simple, yielding relatively poor correlations (e.g. R2 = 0.29 between <ΔpKa [His]> and subcellular pH), and this line of enquiry was not pursued further.
Having established that the predicted and averaged ionisation properties of histidine sidechains are strongly correlated with subcellular environment, but also bearing in mind that average isoelectric points show some correlation, we investigated further the role of histidine positioning in protein structures. Figure 5(a) illustrates a scheme in which, for each protein, acid and base charges other than histidine are fixed and the ionisable groups of histidine explore alternate surface locations (see also the Methods section). One hundred passes were made through the entire dataset, randomising the location of histidine sidechain charge for each protein and recalculating ΔpKas. In order to make these computations feasible, estimates of ΔpKa from full Monte Carlo sampling were substituted by summation of acid/base interactions at each histidine site, assuming protonated bases and deprotonated acids. For the set of non-randomised proteins, this procedure gave the same R2 (0.92) for <ΔpKa [His]> versus subcellular pH, as did the results of Monte Carlo sampling displayed in Figure 4(a), and the <ΔpKa [His]> values themselves correlated with R2 = 0.999 between the two calculations. Figure 5(b) shows that the correlation with subcellular pH, for calculations with the real distribution of histidine ionisable groups, exceeds that for the randomisations. The net charge of a protein can influence His ΔpKa, simply due to an environment weighted towards positive or negative charge, i.e. positive overall destabilises histidine protonation leading to negative His ΔpKas, and a negatively charged background stabilises His protonation, giving positive His ΔpKas. Indeed, the net charge has some correlation with subcellular pH, as seen in Table 1 and Figure 3(a), whereas Figure 5 demonstrates that an additional element of correlation with subcellular pH is attributable to histidine location, beyond the net charge background (which remains constant in the randomisations). Reinforcing this conclusion, R2 for the correlation between the average of net charge on a protein (excluding histidine), over subcellular location, and subcellular pH is 0.42, substantially less than that for <ΔpKa [His]> and subcellular pH of 0.92. Next we consider the physiological context for our observations.
Relevance of correlation between Histidine pKas and subcellular pH
We have found that protein populations tend towards their most stable, on average, at the pH of the relevant subcellular environment. A couple of notes should be made about these results, which are based on predictions of pH-dependent properties from protein structures. The calculation model is simple (Debye-Hückel), based largely on geometry of the charge network. This works well for groups at the protein surface, with charge-charge interactions dominated by water, which is the vast majority of ionisable groups. In addition, the linear correlation of predicted properties with subcellular pH is good, but the fit between these properties and actual subcellular pH values falls away for the acidic vacuolar and lysosomal compartments (Figure 3(b)). We presume that in these cases the restrictions imposed by overall ionisation regions (Figure 2) prevent realisation of more acidic average values.
Taking the basic observation, of predicted maximal stability at subcellular pH, it is important to note that the bimodal distribution of individual protein pH [ΔGFU(min)] values means that generally each protein is not most stable at the pH of its surroundings i.e. the observed correlation relates to a sum over proteins in a particular environment. If this correlation were not observed, then in principle the folding free energy of proteins could (on average) be more stabilising at an alternate pH. Thus, with the observed correlation, the unfolded population of proteins is (on average) minimised with respect to subcellular pH. However, pH-dependent changes in ΔGFU for each protein, and related alteration in the F/U population, are generally small, but possibly could be significant over the subcellular population of proteins. This is a protein folding perspective on the results.
An alternative view would be to consider protonation, pH buffering and pH homeostasis, which is directly related to protein folding since ∂ΔGFU/∂pH αΔQFU . The regulation of pH is of critical importance  and histidine imidazoles are important components of intracellular buffering power . Histidine ΔpKas underpin the relationships that we observe in the current work. In overall terms, we see that more acidic environments tend towards more acidic pH [ΔGFU(min)], which in turn relates to higher His pKas, more positive His ΔpKas and relatively stabilised protonated states. For example, His pKas move towards higher values, away from the subcellular pH, for acidic compartments relative to other environments. The general trend is thus to reduce the buffering power associated with His, in each location. However, this movement is small. Taken as an average value per His, the total range of pKa shift between most acidic and most basic environments is about 0.2 pH unit. Although histidine ionisation properties underlie our results, it may be that their direct contributions to proton/pH buffering are not the most important factor.
The reason that small average changes in His pKa give rise to larger changes in <pH [ΔGFU(min)]> (displayed schematically in Figure 2), is that the stability term includes a difference to the U state, and therefore also to the model compound pKa for His (6.3). Of key importance is ΔpKa, determined by charge interactions in the F state, so that if the model compound value changes, the overall result remains. Thus far we have discussed our results in the context of overall protein stability and pH buffering. Next we combine these aspects.
When a protein folds or unfolds it may release or take-up protons. Another way of looking at the correlations we find is that, on average and with the caveat about acidic compartments not falling directly on the line in Figure 3(b), net proton release or up-take is predicted to be close to zero upon folding or re-folding. However, this need not be the case generally, since metabolic processes leading to net changes in proton concentration are handled by the mechanisms of pH homeostasis .
Outside of net changes in protein folding, and without considering intrinsically unstructured proteins , a subset of proteins or domains will be unfolded at any given time. It is of interest to estimate the number of histidines associated with this unfolded population. Given a protein density of about 1.35 g cm-3 , a volume fraction of around 15% for proteins in the cytoplasm , and an average amino acid molecular weight of 110 daltons, the cytoplasm is approximately 1.8 Molar in protein amino acids. With an estimate of histidine amino acid composition at about 2.3% , this gives a histidine Molarity of 0.042. If an average folded state stability is taken at around 25-30 kJ/mole , then about 1 in 105 domains will be unfolded, so that an approximate concentration of histidine in the unfolded state is 4 × 10-7 Molar. Thus the sub-population of histidine ionisable groups that are transiently in the unfolded state could be larger than the concentration of protons. Of itself this may not be a problem, since transient changes across a compartment will average out. What could be an issue though, is whether changes in the populations of folded and unfolded histidine sites couple to local pH-dependent phenomena. This may be protein folding itself, for example with low numbers of protons at pH 7, fluctuations could impede protein refolding that is associated with proton uptake. Alternatively, the mechanisms of pH-sensing and pH homeostasis could be inappropriately activated and modulated by sufficiently large fluctuations. Whether these processes occur in vivo depends on the details of protein and proton diffusion properties as well as on pH-sensing mechanisms, and their response functions, all of which are unknown at the required level of detail. However, the observed tendency to average protonation changes towards zero for protein folding/unfolding, in each subcellular location, would mitigate against such processes.
In this work we have asked whether the pH-dependence of organelle sub-proteomes, derived with structure-based predictions, correlates with environmental pH. We find that restrictions imposed by the composition of ionisable groups means that individual proteins have minima in pH-dependence, (the predicted pH at maximal stability), that tend to lie on either side of subcellular pH. Averages over proteins within each subcellular location though reveal a strong correlation with subcellular pH. Investigating further it is found that histidine ionisations and ΔpKas from charge interactions in the folded state underlie this correlation.
While net charge and pI also correlate with subcellular pH, and pI correlates with the pH-dependent properties reported here, the strongest relationship is found between pH-dependence (and histidine ΔpKas) and subcellular pH. Thus, while a net charge relationship with subcellular pH could be understood in terms of solubility and avoiding isoelectric aggregation, there is also the question of what lies behind the observed correlation of predicted pH-dependence and subcellular pH. At face value, it could be simply that folding stability tends towards maximal in each subcellular location. However, it is only the average that gives the correlation, rather than the stability maxima for individual proteins.
We have shown that histidine ionisation underlies the pH-dependence correlation. Further, histidine locations are key since random placement of equivalent numbers of histidines, in preserved charge backgrounds, does not reproduce the strength of correlation. This leads us to consider the proton buffering of histidine, but the differences between subcellular environments (i.e. how much histidine ΔpKas are predicted to move) are relatively small.
Finally, we address the role of histidine ionisation in protein folding/unfolding. The direct implication of our results is a prediction that proton release and proton uptake are balanced in a random subset of folding or unfolding proteins. Presumably such a balance would not be required during net protein synthesis or degradation, since the mechanisms of pH homeostasis regulate proton concentration. We speculate that a balance of proton uptake and release could play a role in guarding against activation of pH homeostatic processes during folding and unfolding fluctuations in a steady state subcellular compartment. This can be examined experimentally, with more detailed characterisation of the dynamics of pH homeostasis mechanisms, and computationally with systems level models. It will also be of interest to study the subcellular and extracellular distribution of protonation changes upon complexation. This extends to protein-protein complexation  and to protein-small molecule, for example the Bohr effect in hemoglobin .
Release 55.5 of UniProtKB/Swiss-Prot  was searched for annotation according to the following subcellular compartments: nucleus; vacuole; cytoplasm; extracellular; lysosome; chloroplast; mitochondrion; endoplasmic reticulum; peroxisome; Golgi. Entries with uncertain keywords such as similar, potential, probable were omitted. Requiring at least one cross-reference from the Protein Data Bank (PDB) structural database  gave 5278 UniProt entries referencing 16311 PDB identifiers. These PDB identifiers were filtered using the PISCES server  for X-ray diffraction structures better than 3 Å resolution, a minimum chain length of 30 amino acids and redundancy at 90% sequence identity, yielding 3,713 protein chains. The 90% sequence filter was chosen so that identical chains would be eliminated, but allowing for amino acid variation on a common fold, since the calculated charge interactions will change with such variation. Of the 3,713 chains, we excluded those with extracellular (1,048) and chloroplast (90) annotation, as these locations present a broad pH distribution. A further 534 were annotated with more than one subcellular location and were also excluded, as well as 20 failures in the calculation scheme (for example, due to non-standard residue names). Structure-based predictions of pH-dependent properties were made for the remaining 2,021 protein chains (see Additional file 1), roughly double the number compared with previous work . Figure 1 summarises this dataset.
Continuum models are commonly used for calculating charge interactions in biomolecules. The complexity and computational requirements of these models varies according to the accuracy with which the boundary between solute and solvent is described. In the current work, we require a relatively fast method, enabling calculations not just for many proteins, but also for a randomised dataset that is generated to evaluate the central hypothesis. A simple Debye-Hückel method is sufficient for these purposes, since most of the ionisable charge proteome is exposed to solvent, with water dominating the solvation response . In earlier work in this area, it was found that the relatively simple Debye-Hückel method gave very similar results to the more computationally demanding Finite Difference Poisson-Boltzmann method . A uniform relative dielectric of 78.4 and an ionic strength of 0.15 Molar were used in calculations of charge interactions. To compute ionisable group pKas  from these interactions, Monte Carlo sampling of protonation states was used . Changes in folding energy were derived from the charge difference between folded (F) and unfolded (U) states of a protein (ΔQFU) , with an origin set from the ionisable group contribution to the folding energy calculated at an extreme pH with the reduced sites method . The following model compound pKas were used; sidechains: Asp 4.0; Glu 4.4; His 6.3; Lys 10.4; Arg 12.0; terminal groups: N-terminal 7.5; C-terminal 3.8. Cysteine and tyrosine ionisation has not been considered, since although important in certain catalytic processes, these ionisations are of less interest in a study of global charge properties around neutral pH. The unfolded state is approximated as lacking interactions between ionisable groups. While there are known to be charge interactions in the U state , the current work focuses on the relationship between pKas in the folded state (histidine in particular) and subcellular location. Of interest is that ionisable group interactions in the unfolded state appear to be dominated by local sequence neighbours, in part recapitulating the interactions of the folded state . We trialled a simple model for pKa changes in the unfolded state  as a mimic for folded state pKas, examining whether the correlations observed with subcellular pH were reproduced. If this had been successful, it would have broadened the study to bypass protein structure in examining proteomes; however this trial failed, with substantially lower correlation observed between calculated properties and subcellular pH, compared with structure-based calculations.
An additional test of the Debye-Hückel-based method for calculating maximal stability was made, following a protocol established in previous work . Briefly, the BRENDA enzyme database  was searched for text strings associated with maximal or optimal pH of stability, and these results cross-referenced with PDB entries for the same species and enzyme. The literature references retrieved from BRENDA were checked for data pertaining to a well-defined optimum, rather than a pH-range, and also for confirmation of the optimum in relation to stability as opposed to activity. Additional file 2 gives information for the 19 enzymes retrieved in this analysis. The listed criteria, and in particular the requirement for a precise species match between structure and stability data, leads to a smaller dataset than that reported previously . The calculated root mean square deviation between calculated and experimental pH stability optima is 0.78 for the dataset of 19 enzymes, comparable with the value of 0.72 for the earlier work , and supporting the use of Debye-Hückel modelling in this study.
The quantity His/(Acid + Base) was calculated as the number of histidine residues divided by the sum of Asp, Glu, Lys and Arg residues. In many cases, averages of properties were calculated over a set of protein structures annotated with a particular subcellular location, and denoted by <> symbols.
In order to test the importance of histidine sidechains, predictions of pH dependence for proteins were made with the ionisable charges of histidine sidechains removed. Additional tests made use of proteins that conserved the number of histidine sidechain charges, but not their locations. Their positions were randomly assigned to surface atoms (within amino acids of accessible surface area > 5 Å 2), ensuring ionisable charges were separated by at least 3.5 Å. This distance constraint applied also to the background acidic and basic groups whose locations were unchanged. One hundred datasets of proteins (each mirroring the 2,021 proteins of the wild-type dataset) were constructed in this way, and pH-dependent features calculated. The extent of these computations required us to look at whether the full Monte Carlo sampling, to obtain pKas, could be circumvented for the properties of interest. It was established that the pKa deviations of histidine sidechains (ΔpKa = pKa - pKa [model compound]) could be estimated accurately (in relation to the Monte Carlo sampling) from summation of charge interactions at each ionisable site, at neutral pH (see Results and Discussion).
Experimentally-determined pH values for subcellular compartments were collated from various sources in previous work , with an update for vacuolar pH to reflect its position in the organelle acidification pathway [52, 53]: nucleus 7.7; vacuole 5.3; cytoplasm 7.3; lysosome 4.8; mitochondrion 7.5; endoplasmic reticulum 7.1; peroxisome 8.2; Golgi 6.6. There will be some uncertainty in precise values for individual locations, for example due to compartmentalisation, but the overall trend of more acidic, neutral, or more basic compartments is the key factor.
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Project name: Proteomepk
Project home page: http://www.bioinf.manchester.ac.uk/proteomepk/
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Dinger ME, Pang KC, Mercer TR, Mattick JS: Differentiating protein-coding and noncoding RNA: challenges and ambiguities. PLoS Comput Biol. 2008, 4 (11): e1000176-10.1371/journal.pcbi.1000176.
Mata J, Marguerat S, Bahler J: Post-transcriptional control of gene expression: a genome-wide perspective. Trends Biochem Sci. 2005, 30 (9): 506-514. 10.1016/j.tibs.2005.07.005.
Levy ED, Pereira-Leal JB: Evolution and dynamics of protein interactions and networks. Curr Opin Struct Biol. 2008, 18 (3): 349-357. 10.1016/j.sbi.2008.03.003.
Mo ML, Palsson BO: Understanding human metabolic physiology: a genome-to-systems approach. Trends Biotechnol. 2009, 27 (1): 37-44. 10.1016/j.tibtech.2008.09.007.
Monsellier E, Ramazzotti M, Taddei N, Chiti F: Aggregation propensity of the human proteome. PLoS Comput Biol. 2008, 4 (10): e1000199-10.1371/journal.pcbi.1000199.
Tompa P, Prilusky J, Silman I, Sussman JL: Structural disorder serves as a weak signal for intracellular protein degradation. Proteins. 2008, 71 (2): 903-909. 10.1002/prot.21773.
Sharabiani MT, Siermala M, Lehtinen TO, Vihinen M: Dynamic covariation between gene expression and proteome characteristics. BMC Bioinformatics. 2005, 6: 215-10.1186/1471-2105-6-215.
Rajalahti T, Huang F, Klement MR, Pisareva T, Edman M, Sjostrom M, Wieslander A, Norling B: Proteins in different Synechocystis compartments have distinguishing N-terminal features: a combined proteomics and multivariate sequence analysis. J Proteome Res. 2007, 6 (7): 2420-2434. 10.1021/pr0605973.
Nash R, Weng S, Hitz B, Balakrishnan R, Christie KR, Costanzo MC, Dwight SS, Engel SR, Fisk DG, Hirschman JE, et al: new pages and proteome browser. Nucleic Acids Res. 2007, D468-471. 10.1093/nar/gkl931. 35 Database
Salaman MR, Warwicker J: Anomalies in the ionic properties of serum albumin. Proteins. 2005, 61 (3): 468-472. 10.1002/prot.20628.
Urquhart BL, Atsalos TE, Roach D, Basseal DJ, Bjellqvist B, Britton WL, Humphery-Smith I: 'Proteomic contigs' of Mycobacterium tuberculosis and Mycobacterium bovis (BCG) using novel immobilised pH gradients. Electrophoresis. 1997, 18 (8): 1384-1392. 10.1002/elps.1150180813.
VanBogelen RA, Schiller EE, Thomas JD, Neidhardt FC: Diagnosis of cellular states of microbial organisms using proteomics. Electrophoresis. 1999, 20 (11): 2149-2159. 10.1002/(SICI)1522-2683(19990801)20:11<2149::AID-ELPS2149>3.0.CO;2-N.
Schwartz R, Ting CS, King J: Whole proteome pI values correlate with subcellular localizations of proteins for organisms within the three domains of life. Genome Res. 2001, 11 (5): 703-709. 10.1101/gr.GR-1587R.
Kawashima T, Amano N, Koike H, Makino S, Higuchi S, Kawashima-Ohya Y, Watanabe K, Yamazaki M, Kanehori K, Kawamoto T, et al: Archaeal adaptation to higher temperatures revealed by genomic sequence of Thermoplasma volcanium. Proc Natl Acad Sci USA. 2000, 97 (26): 14257-14262. 10.1073/pnas.97.26.14257.
Knight CG, Kassen R, Hebestreit H, Rainey PB: Global analysis of predicted proteomes: functional adaptation of physical properties. Proc Natl Acad Sci USA. 2004, 101 (22): 8390-8395. 10.1073/pnas.0307270101.
Kiraga J, Mackiewicz P, Mackiewicz D, Kowalczuk M, Biecek P, Polak N, Smolarczyk K, Dudek MR, Cebrat S: The relationships between the isoelectric point and: length of proteins, taxonomy and ecology of organisms. BMC genomics. 2007, 8: 163-10.1186/1471-2164-8-163.
Sun Q, Emanuelsson O, van Wijk KJ: Analysis of curated and predicted plastid subproteomes of Arabidopsis. Plant Physiol. 2004, 135 (2): 723-734. 10.1104/pp.104.040717.
Wu S, Wan P, Li J, Li D, Zhu Y, He F: Multi-modality of pI distribution in whole proteome. Proteomics. 2006, 6 (2): 449-455. 10.1002/pmic.200500221.
Carugo O: Isoelectric points of multi-domain proteins. Bioinformation. 2007, 2 (3): 101-104.
Chan P, Lovric J, Warwicker J: Subcellular pH and predicted pH-dependent features of proteins. Proteomics. 2006, 6 (12): 3494-3501. 10.1002/pmic.200500534.
Orengo CA, Thornton JM: Protein families and their evolution-a structural perspective. Annual review of biochemistry. 2005, 74: 867-900. 10.1146/annurev.biochem.74.082803.133029.
Greaves RB, Warwicker J: Mechanisms for stabilisation and the maintenance of solubility in proteins from thermophiles. BMC Struct Biol. 2007, 7: 18-10.1186/1472-6807-7-18.
Bray T, Doig AJ, Warwicker J: Sequence and Structural Features of Enzymes and their Active Sites by EC Class. J Mol Biol. 2009, 386 (5): 1423-1436. 10.1016/j.jmb.2008.11.057.
Wada A, Nakamura H: Nature of the charge distribution in proteins. Nature. 1981, 293 (5835): 757-758. 10.1038/293757a0.
Pace CN, Grimsley GR, Scholtz JM: Protein ionizable groups: pK values and their contribution to protein stability and solubility. J Biol Chem. 2009, 284 (20): 13285-13289. 10.1074/jbc.R800080200.
Berenbrink M: Evolution of vertebrate haemoglobins: Histidine side chains, specific buffer value and Bohr effect. Respiratory physiology & neurobiology. 2006, 154 (1-2): 165-184. 10.1016/j.resp.2006.01.002.
Warwicker J, Watson HC: Calculation of the electric potential in the active site cleft due to alpha-helix dipoles. J Mol Biol. 1982, 157 (4): 671-679. 10.1016/0022-2836(82)90505-8.
Kim J, Mao J, Gunner MR: Are acidic and basic groups in buried proteins predicted to be ionized?. J Mol Biol. 2005, 348 (5): 1283-1298. 10.1016/j.jmb.2005.03.051.
Warwicker J: Simplified methods for pKa and acid pH-dependent stability estimation in proteins: removing dielectric and counterion boundaries. Protein Sci. 1999, 8 (2): 418-425.
Warwicker J: Improved pKa calculations through flexibility based sampling of a water-dominated interaction scheme. Protein Sci. 2004, 13 (10): 2793-2805. 10.1110/ps.04785604.
Alexov E: Numerical calculations of the pH of maximal protein stability. Eur J Biochem. 2004, 271 (1): 173-185. 10.1046/j.1432-1033.2003.03917.x.
Weiller GF, Caraux G, Sylvester N: The modal distribution of protein isoelectric points reflects amino acid properties rather than sequence evolution. Proteomics. 2004, 4 (4): 943-949. 10.1002/pmic.200200648.
Antosiewicz J, McCammon JA, Gilson MK: Prediction of pH-dependent properties of proteins. J Mol Biol. 1994, 238 (3): 415-436. 10.1006/jmbi.1994.1301.
Oliveberg M, Arcus VL, Fersht AR: pKA values of carboxyl groups in the native and denatured states of barnase: the pKA values of the denatured state are on average 0. Biochemistry. 1995, 34 (29): 9424-9433. 10.1021/bi00029a018.
Boron WF: Regulation of intracellular pH. Advances in physiology education. 2004, 28 (1-4): 160-179. 10.1152/advan.00045.2004.
Abe H: Role of histidine-related compounds as intracellular proton buffering constituents in vertebrate muscle. Biochemistry (Mosc). 2000, 65 (7): 757-765.
Demaurex N: pH Homeostasis of cellular organelles. News Physiol Sci. 2002, 17: 1-5.
Dunker AK, Silman I, Uversky VN, Sussman JL: Function and structure of inherently disordered proteins. Curr Opin Struct Biol. 2008, 18 (6): 756-764. 10.1016/j.sbi.2008.10.002.
Quillin ML, Matthews BW: Accurate calculation of the density of proteins. Acta crystallographica. 2000, 56 (Pt 7): 791-794.
Sear RP: The cytoplasm of living cells: a functional mixture of thousands of components. Journal of Physics-Condensed Matter. 2005, 17 (45): S3587-S3595. 10.1088/0953-8984/17/45/052.
Jukes TH, Holmquist R, Moise H: Amino acid composition of proteins: Selection against the genetic code. Science (New York, NY). 1975, 189 (4196): 50-51.
Pace CN, Trevino S, Prabhakaran E, Scholtz JM: Protein structure, stability and solubility in water and other solvents. Philosophical transactions of the Royal Society of London. 2004, 359 (1448): 1225-1234. 10.1098/rstb.2004.1500. discussion 1234-1225
Kundrotas PJ, Alexov E: Electrostatic properties of protein-protein complexes. Biophys J. 2006, 91 (5): 1724-1736. 10.1529/biophysj.106.086025.
Riggs AF: The Bohr effect. Annual review of physiology. 1988, 50: 181-204. 10.1146/annurev.ph.50.030188.001145.
Leinonen R, Nardone F, Zhu W, Apweiler R: UniSave: the UniProtKB sequence/annotation version database. Bioinformatics. 2006, 22 (10): 1284-1285. 10.1093/bioinformatics/btl105.
Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000, 28 (1): 235-242. 10.1093/nar/28.1.235.
Wang G, Dunbrack RL: a protein sequence culling server. Bioinformatics. 2003, 19 (12): 1589-1591. 10.1093/bioinformatics/btg224.
Bashford D, Karplus M: pKa's of ionizable groups in proteins: atomic detail from a continuum electrostatic model. Biochemistry. 1990, 29 (44): 10219-10225. 10.1021/bi00496a010.
Beroza P, Fredkin DR, Okamura MY, Feher G: Protonation of interacting residues in a protein by a Monte Carlo method: application to lysozyme and the photosynthetic reaction center of Rhodobacter sphaeroides. Proc Natl Acad Sci USA. 1991, 88 (13): 5804-5808. 10.1073/pnas.88.13.5804.
Tan YJ, Oliveberg M, Davis B, Fersht AR: Perturbed pKA-values in the denatured states of proteins. J Mol Biol. 1995, 254 (5): 980-992. 10.1006/jmbi.1995.0670.
Chang A, Scheer M, Grote A, Schomburg I, Schomburg D: BRENDA, AMENDA and FRENDA the enzyme information system: new content and tools in 2009. Nucleic Acids Res. 2009, D588-592. 10.1093/nar/gkn820. 37 Database
Huynh KK, Grinstein S: Regulation of vacuolar pH and its modulation by some microbial species. Microbiol Mol Biol Rev. 2007, 71 (3): 452-462. 10.1128/MMBR.00003-07.
Kulichikhin KY, Greenway H, Byrne L, Colmer TD: Regulation of intracellular pH during anoxia in rice coleoptiles in acidic and near neutral conditions. Journal of experimental botany. 2009, 60 (7): 2119-2128. 10.1093/jxb/erp090.
The authors acknowledge support from the UK BBSRC, and thank Tracey Bray, Salim Bougouffa, James Kitchen and Andrew Cawley for discussions on this work.
JW and PC together designed the study and wrote code for the calculations. The dataset was assembled by PC, and PC performed the calculations and most of the data analysis. JW and PC together wrote the paper.
Electronic supplementary material
Additional file 1: Dataset. An Excel file containing the PDB and chain identifiers, and subcellular annotations, of proteins used in this work is provided. The data follow the description given in Figure 1. (XLS 411 KB)
Additional file 2: pH of max stability. Information for the proteins used in a test of pH stability predictions. (XLS 14 KB)
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Chan, P., Warwicker, J. Evidence for the adaptation of protein pH-dependence to subcellular pH . BMC Biol 7, 69 (2009). https://doi.org/10.1186/1741-7007-7-69
- Ionisable Group
- Charge Interaction
- Folding Energy
- General Bimodality