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Fish Physiology and Biochemistry

, Volume 34, Issue 1, pp 1–8 | Cite as

The isoelectric point, a key to understanding a variety of biochemical problems: a minireview

  • F. M. A. H. Schuurmans StekhovenEmail author
  • M. H. A. G. Gorissen
  • G. Flik
Open Access
Article

Abstract

We address the importance of the isoelectric point (IEP) of proteins and membrane components such as phospholipids for our understanding and interpretation of isoforms and opposite charge interactions in the formation of complexes. Five examples drawn from the literature are newly approached from the IEP point of view to clarify general principles.

Keywords

Isoelectric point Isoforms Protein–protein Protein–phospholipid complexes 

Introduction

The isoelectric point (IEP) of a protein is generally considered to be a mere physicochemical property that results from the summed ambivalent charge properties of its amino acid constituents. In fact, the IEP values of proteins are often not even recorded in data books, despite the primary structure of the protein being fully known. We show here that the IEP is a powerful tool to predict and understand interactions between proteins, proteins and membranes (phospholipids) or to determine the presence of protein isoforms.

In this paper we will address five topics/examples from our published research:
  1. 1.

    multi-isoelectric appearance of a glycoproteinaceous hormone, stanniocalcin;

     
  2. 2.

    charge interaction in the activation of the melanocortin-1 receptor (MC-R1) by its hormone α-melanophore-stimulating hormone (MSH);

     
  3. 3.

    evidence for post-translationally modified isoforms of the phospholemman in rectal glands of a shark, the spiny dogfish;

     
  4. 4.

    evaluation of the interaction between energy-coupling factor B and the proton channel in the mitochondrial ATP synthase complex;

     
  5. 5.

    complexation of extranuclear histones to negative phospholipids in the plasma membrane following cell injury of fish gills.

     

Procedures

Calculation of the IEP

The charge of a protein is a resultant of residues that at a given pH become charged when they lose a proton: (1) \(\hbox{RH} \leftrightarrow \hbox{R}^{-}+ \hbox{H}^{+}\;\hbox{KDa}= \frac{\left[\hbox{R}^{-}\right]\left[\hbox{H}^{+}\right]} {\left[\hbox{RH}\right]} \rightarrow [\hbox{R}^{-}]= \frac {\hbox{KDa[RH]}} {[\hbox{H}^{+}]}\) (setting [H+] = x yields \([\hbox{R}^{-}]= \frac{\hbox{KDa[RH]}}x\)), and by residues that become uncharged when they lose a proton: (2) \(\hbox{R}^{\prime}\hbox{H}^{+}\leftrightarrow \hbox{R}^{\prime} + \hbox{H}^{+}\; \hbox{KDb}= \frac {\left[\hbox{R}^{\prime}\right]\left[\hbox{H}^{+}\right]} {\left[\hbox{R}^{\prime}\hbox{H}^{+}\right]}= \frac{\left[\hbox{R}^{\prime}\right]x} {\left[\hbox{R}^{\prime}\hbox{H}^{+}\right]}\rightarrow \left[\hbox{R}^{\prime}\hbox{H}^{+}\right]= \frac {\left[\hbox{R}^{\prime}\right]x}{\hbox{KDb}}\) . Further: [RH] +  [R] =  c (concentration of a single residue) and [R′H+] +  [R′] = c. Hence,
$$ [\hbox{R}^{-}] = \frac{\hbox{KDa}\left\{c- \left[\hbox{R}^{-}\right]\right\}} {x}\rightarrow [\hbox{R}^{-}]x = \hbox{KDa.c}-\hbox{KDa}[\hbox{R}^{-}] \rightarrow(x + \hbox{KDa)}[\hbox{R}^{-}] = \hbox{KDa}.\hbox{c} \rightarrow [\hbox{R}^{-}] = \frac{\hbox{KDa.c}}{x+\hbox{KDa}} = \frac{c}{1+\frac{x}{\hbox{KDa}}}\\. $$
(1)
Similarly:
$$ [\hbox{R}^{\prime}\hbox{H}^{+}] = c - [\hbox{R}^{\prime}]= c - \frac{\left[\hbox{R}^{\prime}\hbox{H}^{+}\right] \cdot \hbox{KDb}}{x} = \frac {cx- \left[\hbox{R}^{\prime}\hbox{H}^{+}\right] \cdot \hbox{KDb}}{x}\rightarrow [\hbox{R}^{\prime}\hbox{H}^{+}] = \frac {cx}{\hbox{Kdb}+x} = \frac{c}{1+\frac{\hbox{KDb}}{x}} $$
(2)
.
In the IEP [R] − [R′H+] =  0, hence \(\frac{c}{1+\frac{x}{\hbox{KDa}}}- \frac{c}{1+\frac{\hbox{KDb}}{x}} = 0 \rightarrow \frac {1}{1+\frac{x}{\hbox{KDa}}}- \frac {1}{1+\frac{\hbox{KDb}}{x}} = 0.\) Since total charge is the algebraic sum of all charged residues, one obtains for the IEP
$$ \mathop\Sigma\limits^{i}_{1} \frac{n_{j}}{1+\frac{x}{\hbox{KDa}_{i}}} -\mathop\Sigma\limits^{j}_{1}\frac{m_{j}}{1+\frac{\hbox{KDb}_{j}}{x}}= 0 $$
(3)
.

This equation is identical to the formulation given by Sillero and Ribeiro (1989): \(\mathop\Sigma\limits^{p}_{i=1}\frac{1}{1+10^{\rm pH-pKPi}} - \mathop\Sigma\limits^{n}_{i=1}\frac{1}{1+10^{\rm pKNi-pH}} = 0\) with pKPi being equivalent to −10log KDbj and pKNi equivalent to −10logKDai. We use Eq. 3 and determine the IEP graphically from the intersection with the axis of zero charge difference in the Δcharge versus pH chart. The EMBL website gateway to IEP service (http://www.embl-heidelberg.de/cgi/pi-wrapper.pl) gives similar results with a maximal deviation of only a few percentage. On the other hand, the programme WinPep (http://www.ipw.agrl.ethz.ch/∼lhennig/winpep.html) gives totally different – often too low – figures, and has been avoided here for the calculation of the IEP. However, this programme is reliable for the calculation of the hydropathy plot according to the procedure of Kyte and Doolittle (1982), which was applied to determine the membrane-traversing moieties of the proteins discussed.

KDa and KDb values were derived in general from the Handbook of Chemistry and Physics (Lide 1998): 2 × 10−2–4.17 × 10−3 for KDa of the α-COOH group (histidine–tryptophan), 1.94 × 10−4 for the β-carboxyl of aspartic acid, 7.08 × 10−5 for the γ-carboxyl of glutamic acid, 7.24 × 10−9 for the sulfhydryl of cysteine, 7.94 × 10−11 for the tyrosyl OH-group, 2 × 10−6 for the phosphoryl group of phosphoserine or phosphothreonine, 1.1 × 10−9–3.4 × 10−11 for the α-NH 3 + (threonine-proline), 7.94 × 10−13 for the guanidyl group of arginine, 9.12 × 10−7 for the imidazole group of histidine and 2.13 × 10−11 for the ɛ-NH 3 + of lysine. The KD-values for the functional groups of phosphatidylserine: \((3.16-7.94)\times10^{-4}(\hbox{O=}\mathop{\hbox{P}}\limits^{\vert}_{\vert}-\hbox{OH}), 3.98\times10^{-5}\) (–COOH), and 1.58 × 10−10 (–NH 3 + ) were taken from van Dijck et al. (1978). In the calculation of the IEP of phospatidylserine the term \(\frac{1}{1+\hbox{KDb/}x}\) reduces to 1 because of the negligibility of the term KDb/x. This leads to \(\hbox{IEP}= \frac{\hbox{pKa1} + \hbox{pKa2}}{2}\) for this particular case.

Results and discussion

Variability in IEP of trout stanniocalcin

Stanniocalcin is an anti-hypercalcemic glycoproteinaceous hormone (first detected in fish, but since found to be present in all vertebrates) that controls Ca2+ influx via the gills of fish (Flik 1990) and intestine (Sundell et al. 1992); in mammals, it promotes inorganic phosphate (Pi) reabsorption by renal proximal tubules (Lu et al. 1994).

During in vitro synthesis of the hormone stanniocalcin by rainbow trout corpuscles of Stannius, three products of equimolar mass (28 kDa for the mature hormone and 32 kDa for the prohormone monomers) were observed in a two-dimensional electrophoretic protein pattern. Stanniocalcin is homodimeric but yields monomers under the reducing conditions of the Laemmli (1970) gel electrophoresis system that have IEPs of 7, 6.1–6.3, and 5–5.2, respectively (Flik et al. 1990). Since the molecular masses of the products are for all practical purposes the same, the variation in IEP may be due to a variation in the deamidation of Asn-residues (N) or a variation in the acetylation of Lys-residues (K), a possibility not demonstrated to date. We have chosen for the former possibility in view of the fact that glycosylation of the 28-kDa product has been shown to diminish with a decreasing IEP. Figure 1 shows that the IEP of rainbow trout stanniocalcin is negatively correlated with the number of deamidations of the N-residues, with the IEP of 6.1–6.3 corresponding to two deamidations and the IEP of 5–5.2 corresponding with six to eight deamidations. Acetylation of the K-residues would lead to similar results (not shown).
Fig. 1

The calculated isoelectric point (IEP) of the rainbow trout hormone stanniocalcin as a function of deamidation of N-residues. The primary structure of the mature rainbow trout stanniocalcin polypeptide is derived from the SwissProt data bank under accession no. P43648

The biochemical consequence of this decreased IEP is not yet clear, but it may be a signal for metabolic clearance of the hormone that should have a short half-life to fine-tune the Ca2+ influx under variable and varying conditions. To acquire further insight, one should know the IEP of the hormone receptor as it is conceivable that when the IEP of receptor and activator approach each other, their mutual attraction will be minimised. An example of this principle will be given in the third case study presented in a following section (repulsion of phosphorylated phospholemman by the near-isoelectric Na,K-ATPase) below. This concept should be taken into consideration in future evaluations of the function of the stanniocalcin receptor, which awaits molecular demonstration. Only circumstantial evidence is currently available that stanniocalcin signals through a G-protein-coupled plasma membrane receptor (Flik 1990).

Hormone–receptor interactions between α-MSH and MC-R1

Another pertinent example of charge interaction between functionally active proteins is the binding of α-MSH to the MC-R1, which occurs through the stepwise activation of adenylate cyclase, protein kinase A and tyrosinase to the final formation of the skin pigment melanin (Rozaud and Hearing 2005) and its rapid dispersion in the cell in background adaptation. A revealing recent finding is that the functional difference in teleost skin pigmentation (dorsal dark, ventral light) is due to a ventral localization of the melanocortin antagonist ASP (Agouti-Signaling Protein) (Cerdá-Reverter et al. 2005). This has lead to the interesting question of whether the IEPs of agonist (α-MSH), antagonist (ASP) and receptor (MC-R1) have a predictive value for their interaction.

α-MSH is the C-terminally amidated O-acetylated peptide AcSYSMEHFRWGKPV-NH2 with a calculated IEP of 10.4. ASP (from the cyprinid Carassius auratus) comprises 125 residues (Cerdá-Reverter et al. 2005) but does not show any sequence similarity to the agonist α-MSH. The hydropathy plot of ASP reveals an N-terminus (M1-V20) that should be able to penetrate the membrane and provide ASP with the capability for a more stable binding with the receptor than can be achieved by α-MSH. The calculated IEP of ASP is 8.71, 1.7 units lower than that of α-MSH, but still quite alkaline. The receptor MC-R1 from Danio rerio (another cyprinid) contains seven transmembrane helices and four extracellular segments (M1-Q47, N96-N123, Y187-D190, H262-H281) with calculated IEPs of 6.3, 4.3, 4.9 and 10.0, respectively (Fig. 2a). One would predict that the positively charged hormone binds to one or more of the extracellular segments with an acidic IEP (segment 1, 2 or 3). In human MC-R1, the first 28 residues can be deleted without any effect on hormone binding (Schiöth et al. 1997), providing strong evidence that the first extracellular segment is an unlikely candidate for hormone–receptor interaction. In support of this, the first extracellular segment of the human receptor has a calculated IEP of 11.8 (Fig. 2b) and will therefore repel the positively charged hormone, while it may have directing properties. The other extracellular segments have calculated IEP values that are commensurate to the counterparts in Danio rerio: 3.7 vs. 4.3 for the second segment; 4.9 vs. 4.9 for the third segment, and 8.5 vs. 10.0 for the fourth segment.
Fig. 2

Difference in charge (ΔE; Eq. 3 of Procedures) between acidic and basic amino acids as a function of pH in the extracellular segments of the melanocortin-1 receptor (MC-R1) from Danio rerio (a) and human (b). Segments are indicated on the graphs and their IEP values in the margin to the right

Not surprisingly, the second segment is the most promising candidate for hormone receptor interaction, and this has been confirmed by mutational studies (Frändberg et al. 1994) in which D117 (D122 in Danio rerio) was transformed to the A residue. This D residue normally complexes with H6 in α-MSH (Prusis et al. 1995). A 50% lesser reduction in the efficacy of the hormone was obtained by the mutation of H260 (H262 in Danio rerio) to the A residue, which is situated at the border of the fourth extracellular segment and therefore sufficiently remote from the more basic K278 residue that could have caused overall repulsion of the equally basic hormone. H260 would normally form a complex with E5 of α-MSH, implying that the fourth extracellular segment must fold back in order to reach the E5 residue that is next to the H6 residue of the hormone. The latter consideration makes clear that not only the IEP of a whole segment is predictive for charge interaction but that certain spatial effects are also in control. Therefore, it is possible that the initial (and crucial) interaction in the second segment brings the hormone in a position for interaction with the fourth segment, rather than the reverse. This could explain why the mutation of H260 → A leads to a 50% decrease in activation compared to the mutation of D117→ A (Frändberg et al. 1994).

In ASP at least 1 H (position 23) and 2 E residues (E27, E28) are present in the first ten residues following the N-terminal transmembrane fragment. These may have the binding function, analogous with the function of E5 and H6 in α-MSH, and thus act as competitive inhibitor (Cerdá-Reverter et al. 2005).

Shark rectal gland phospholemman isoforms

Mahmmoud et al. (2000) reported a dual spot of phospholemman (15 kDa) in a two-dimensional gel electrophoretic separation of spiny dogfish rectal gland Na,K-ATPase. Phospholemman may be identical with the cAMP-dependent protein kinase (PKA)-dependent high conductance Cl channel in the apical membrane of this shark (Greger et al. 1985) and is dissociated from its binding to Na,K-ATPase by phosphokinase treatment (Mahmmoud et al. 2000). We determined two IEPs – 7.9 and 8.35 – from a non-linear calibration curve of distance to the origin versus pI of their results (compare Fig. 1 of Mahmmoud et al. 2000). In a subsequent paper, Mahmmoud et al. (2003) presented the full amino acid sequence for the phospholemman, from which we calculate an IEP of 7.84, which is not significantly different from the reported IEP of 7.9 registered for one of the two spots in the earlier study (Mahmmoud et al. 2000). In that article, however, a N-terminal sequence was recorded that differed among the fourth (E→A), 19th (L→K) and 24th (L→K) residues, indicating an isoform of the Cl-channel (Mahmmoud et al. 2003). Assuming that the sequence beyond this stretch of residues had remained unaltered in terms of acidic and basic residues, we calculate an IEP of 9.05. If, however, as the authors also suggest, K19 and K24 were erroneous, we calculate an IEP for the isoform of 8.28, which is near the second IEP of 8.35. The K and L residues are easily misdetermined due to their partial overlap in the chromatographical separation of thiohydantoin derivatives. Peak retention time ranges (25 runs) are 17.52–17.91 min for K and 17.89–18.25 min for L. Similar isoforms with an E or D residue at the N-terminus are found in other sharks of the Triakidae and Lamnidae families (Schuurmans Stekhoven et al. 2001). The A and E isoforms of S. acanthias according to our own data are in a molar ratio of 2:1. Phospholemman may not only differ in the N-terminus, but also in its C-terminus, as was recently demonstrated for a cytoskeleton-bound form of this protein (Kelly et al. 2004).

The reported dissociation of phospholemman from Na,K-ATPase following phosphokinase treatment (Mahmmoud et al. 2000) can be explained by a downward shift in IEP from 7.84 for the non-phosphorylated E4 isoform to 6.2 for its twice phosphorylated form. The latter represents the maximum of phosphorylation known for the mammalian protein (Walaas et al. 1994). This IEP approaches those found for different isozymes of Na,K-ATPase, such as the α-1 subunit (5.3; Google: AFCS protein A002647 – Signalling), the α-2 subunit (5.5; Yamaguchi and Post 1983) and α-3 subunit (5.0–5.3; UniProt: Q90WE7; SWALL: Q9DGL4), which leads to repulsion and dissociation of the complex (Mahmmoud et al. 2000). On the other hand, complexation of the C-terminal moiety of phospholemman to negatively charged phospholipids in the plasma membrane (Clayton et al. 2005) remains warranted (Lansbery et al. 2006) despite the phosphorylation. This mode of regulation through phosphorylation-dependent IEP changes has received only little attention to date.

Factor B’s involvement in proton transport by the ATP-synthase complex

Since its discovery in 1967 (Lam et al. 1967) energy transfer factor B (FB) has been assigned a role in proton transport through the mitochondrial membrane in conjunction with the DCCD-binding protein, also known as subunit c (Sanadi et al. 1984). It has only been fairly recently that the full amino acid sequence of human factor B has been elucidated as a 20.3-kDa protein (Belogrudov and Hatefi 2002). These data allowed us to calculate an IEP of 6.7, which is slightly below the pH of the cytoplasm (6.7–7.4; Schuurmans Stekhoven 1968); the charge of the protein is therefore neutral to slightly negative. Purification of FB by means of carboxymethyl (CM)-cellulose (Lam et al. 1967) would predict a positive charge at pH 7.5, but FB at this stage is still complexed to another protein of higher molecular weight and possibly higher IEP.

Full-size sequencing of the DCCD-binding protein is filed in the SwissProt database under accession #P32876 (isoform 1: 14.2 kDa) and accession #P07926 (isoform 2: 15.0 kDa). The IEP values for their intracellular segments are the same: 11.4. Consequently, each is capable of attracting the FB to form a complex. Yet, upon isolation of ATP-synthase, FB turns out to be absent (Walker et al. 1991; Ko et al. 2003). Given the sensitivity of FB activity to sulfhydryl (SH)-reagents (Lam 1968), it is conceivable that complex formation of FB with the DCCD binding protein occurs by means of a disulfide bridge rather than by electrostatic force. Since the oligomycin-sensitive ATPase complex (OS-ATPase) is usually isolated in the presence of SH-reagents (mercaptoethanol, Walker et al. 1991; dithiothreitol, Ko et al. 2003), it is equally conceivable that FB is being released in the procedure. In addition, the detergents used in these earlier studies may have caused dissociation as has been found, for example, in dissociating phospholemman from NaK-ATPase (Mahmmoud et al. 2000). The DCCD-binding protein contains only two C-residues (C17 and C125 in isoform 1; C3 and C132 in isoform 2) of which C125 and C132 are present in the second transmembrane segment of the protein channel (Fig. 3). Formation of the disulfide linkage can thus take place at C17 (isoform 1) or C3 (isoform 2). In contrast, FB does not traverse the membrane; however, it does contain six C-residues (C33, C71, C92, C94, C101 and C123) that could be involved in disulfide linkage while still leaving enough C residues free for another disulfide bridge that might function as a means of intermediary H+ transport:
$$ \begin{array}{lllll} \hbox{--}\hbox{S}\hbox{--}\hbox{S}\hbox{--} + 2\hbox{e} + 2\hbox{H}^{+} &\leftrightarrow &2 -\hbox{SH}- 2\hbox{e} &\leftrightarrow &\hbox{--}\hbox{S}\hbox{--}\hbox{S}\hbox{--} + 2\hbox{H}^{+}.\\ 1.& & 2.& &3. \end{array} $$
Fig. 3

Hydropathy plot of the DCCD-binding protein (isoform 1, SwissProt accession #P32876), demonstrating the intramembranal segment (M1–K68) with its C17 residue, the first transmembrane (F69–A98) segment, the R99–Q106 extramembranal segment and the second (L107–M136) transmembrane segment. The latter contains the proton-transporting E119 residue and the second C residue of the proton channel

Step 1 would be the delivery of two electrons by the respiratory chain before a site of phosphorylation and step 2 would consist of the removal of two electrons immediately behind this site of phosphorylation. The final step of H+ transport from the intra-mitochondrial space to the outside compartment and vice versa may take place via E119 (isoform 1) or E126 (isoform 2) of the DCCD-binding protein. It should be noted that the involvement of disulfide bridges in energy-linked H+ transport has been suggested earlier by studies on triphenyltin inhibition of CF0-catalysed transmembrane H+ transfer in chloroplasts (Gould 1978). The construction of the proton gradient takes time, and this can be reduced by addition of the SH-reagent dithiothreitol (Schuurmans Stekhoven et al. 1970).

Although the interaction between FB and the DCCD binding protein is probably not of an electrostatic character, but rather of a reversibly covalent (disulfide bridging) one, the IEP considerations have also been decisive in coming to this conclusion in this example.

The phenomenon of extranuclear histones

In a recent search for the Cl channel phospholemman in the microsomal fraction of teleost gills, we found no phospholemman but instead histone and histone fragments in the molecular-weight region on the gel (13–15 kDa) that usually is occupied by phospholemman (Schuurmans Stekhoven et al. 2004). This occurrence outside of the nucleus is designated extranuclear but is generally not found in the 100,000-g sediment, but rather the 100,000-g supernatant, bound to carriers like transportin, importin 5 and importin 9 (Mühlhäusser et al. 2001). These carriers exert a strong electrostatic attraction to histones; for example, transportin-SR displays an IEP of 5.29 (Kataoka et al. 1999), which is far removed from that of histone H2A (Conner et al. 1984), which has a calculated IEP of 11.3, or that of H2B (Winkfein et al. 1985), with a calculated IEP of 10.95. The same holds for the other carriers mentioned: importin 5 (SwissProt accession #Q8BKCS) and importin 9 (SwissProt accession #Q96P70), with calculated IEPs of 4.50 and 4.42, respectively. Only when the cytoplasmic protection of histones by their carriers is removed by activation of autolysis upon skin or gill injury (Cho et al. 2002a, b) or when nuclear import is inhibited (e.g. by lectins, Watson et al. 1995) are histones liberated into the cytoplasm where they will adhere to the cell membrane. One of the components of the cell membrane that is oriented in viable cells to the cytoplasmic face of this membrane (Verkleij et al. 1973) is phosphatidylserine. Its IEP value of 3.75–3.95 is sufficiently low to warrant binding of the positively charged histones, as was the case in our studies.

Conclusion

Our aim has been to provide support, using the examples discussed herein, to the concept that calculation and consideration of the IEP in protein chemical determination studies can lend weight to our understanding of a variety of phenomena. We have presented evidence demonstrating that the presence of isoforms with a different IEP can be deduced from a variation in the balance between acidic and basic amino acid residues within the polypeptide chain (phospholemman isoforms, example 3) or be due to chemical modification (deamidation) of the conserved residues (stanniocalcin isoforms, example 1). Other examples, such as the hormone–receptor interaction, reversible covalent binding and complexation of extremely opposing charges, have also been reported, which, in our opinion, provide sufficient support for the relevance of considering the IEP of the interacting proteins and their segments.

However, we cannot say that the subject of the IEP in relation to charge interactions is neglected in most publications. An example to the contrary is the elucidating explanation of the mechanism of interaction between cytochrome c reductase and cytochrome c oxidase with the intermediary cytochrome c (Stryer 1995). Another example is the release of phospholemman from the endoplasmic reticulum to the plasma membrane upon charge neutralization at the C-terminus by protein kinase C (PKC)-linked phosphorylation (Lansbery et al. 2006). Undoubtedly, other examples can also be found.

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Copyright information

© Springer Science+Business Media B.V. 2007

Authors and Affiliations

  • F. M. A. H. Schuurmans Stekhoven
    • 1
    Email author
  • M. H. A. G. Gorissen
    • 1
  • G. Flik
    • 1
  1. 1.Department of Animal Physiology, Faculty of ScienceRadboud University NijmegenNijmegenThe Netherlands

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