Sedimentation Equilibrium of a Small Oligomer-forming Membrane Protein: Effect of Histidine Protonation on Pentameric Stability

Podsumowanie

Sedimentation equilibrium (SE) can be used to study protein-protein interactions in a physiological environment. This manuscript describes the use of this technique to determine the effect of pH on the stability of a homo-pentamer formed by the small hydrophobic (SH) protein encoded by the human syncytial respiratory virus (hRSV).

Streszczenie

Analytical ultracentrifugation (AUC) can be used to study reversible interactions between macromolecules over a wide range of interaction strengths and under physiological conditions. This makes AUC a method of choice to quantitatively assess stoichiometry and thermodynamics of homo- and hetero-association that are transient and reversible in biochemical processes. In the modality of sedimentation equilibrium (SE), a balance between diffusion and sedimentation provides a profile as a function of radial distance that depends on a specific association model. Herein, a detailed SE protocol is described to determine the size and monomer-monomer association energy of a small membrane protein oligomer using an analytical ultracentrifuge. AUC-ES is label-free, only based on physical principles, and can be used on both water soluble and membrane proteins. An example is shown of the latter, the small hydrophobic (SH) protein in the human respiratory syncytial virus (hRSV), a 65-amino acid polypeptide with a single α-helical transmembrane (TM) domain that forms pentameric ion channels. NMR-based structural data shows that SH protein has two protonatable His residues in its transmembrane domain that are oriented facing the lumen of the channel. SE experiments have been designed to determine how pH affects association constant and the oligomeric size of SH protein. While the pentameric form was preserved in all cases, its association constant was reduced at low pH. These data are in agreement with a similar pH dependency observed for SH channel activity, consistent with a lumenal orientation of the two His residues in SH protein. The latter may experience electrostatic repulsion and reduced oligomer stability at low pH. In summary, this method is applicable whenever quantitative information on subtle protein-protein association changes in physiological conditions have to be measured.  

Wprowadzenie

Analytical ultracentrifugation^1-5 is one of the most important methods to study interactions of macromolecules under physiological conditions, being accessible to both weak and strong interactions. The method is label-free and uses light absorption or interference, and even fluorescence optical systems can be used to access concentration ranges over several orders of magnitude⁶.

This method is especially useful since most biochemical processes depend on reversible interactions. The stoichiometry and strength of these interactions have to be quantitatively characterized to understand biological processes, and a number of methods exist for this purpose ^7,8. However, transient interactions are difficult to study ⁹.

The choice of a method to characterize macromolecular interactions depends on its static or dynamic nature. In the first case, sedimentation velocity (SV) is used, where the rate of radial transport is measured and complexes are fractionated on the basis of differences in buoyant mass and shape.

In contrast, dynamic associations that are reversible on the time scale of the experiment cannot be physically separated. In this case, self- or hetero-interactions leading to non-covalent interactions are in an equilibrium that depends on the total protein concentration. These dynamic interactions can be studied by both sedimentation equilibrium (SE) and sedimentation velocity (SV) ¹⁰. However, the first method is simpler to perform and is described here. In SE, centrifugation is performed at a sufficiently low speed so that an equilibrium is reached between diffusion and sedimentation. At this point, the equilibrium profile of an optical signal (UV-VIS) as a function of radial distance, can be analyzed using pre-set thermodynamic models for associations¹¹.

In the present paper, a sedimentation equilibrium study is presented of the self-association of a viral membrane protein that forms ion channels. Because of its hydrophobicity, the experiment is run in presence of detergent, and in this case the density of solvent has to be matched to that of the detergent. However, the protocol described would identical in the case of a water soluble protein, except that no solvent density matching would be required.

The protein used is encoded in the human respiratory syncytial virus (hRSV), an enveloped pneumovirus in the paramyxoviridae family that causes lower respiratory tract disease in infants, elderly and immunocompromised populations worldwide ¹². Up to 64 million reported cases of hRSV infection and 160,000 deaths occur each year.

The hRSV genome transcribes 11 proteins, including the three membrane proteins F, G, and small hydrophobic (SH). SH protein is involved in the pathogenesis of RSV infection. RSV lacking the SH gene (RSVΔSH) was viable, caused formation of syncytia and grew as well as the wild-type (WT) virus ^13-16. However, RSVΔSH virus replicated 10-fold less efficiently than the WT in the upper respiratory tract ^15,16. Also, RSVΔSH virus was attenuated in in vivo mouse and chimpanzee models ^13,17.

The SH protein is a 64 (RSV subgroup A) or 65 (RSV subgroup B) amino acids long type II integral membrane protein that  accumulates mostly at the membranes of the Golgi compartment ¹⁸.  SH protein has a single predicted a-helical transmembrane (TM) domain ¹⁹ which is highly conserved ^20,21. The C- and N-terminal extramembrane domains are oriented lumenally/extracellularly and cytoplasmically, respectively.

Both synthetic TM domain (residues 18-43) and full length SH protein have been shown to form homopentamers in a variety of detergents. The homopentameric form is responsible for channel activity in planar lipid bilayers ^22,23. The correct orientation of the TM monomers in the lipid bilayer was first determined using site specific infrared dichroism ²³, which showed His-22 to be in a lumenal, close to inter-helical, orientation. The same TM domain orientation was confirmed by NMR studies that reconstructed the pentameric a-helical bundle of the full-length protein in dodecylphosphocholine (DPC) micelles ²². In this ‘micelle’ model, a single a- helical TM domain was flanked N-terminally by an a-helix, and C-terminally by an extended b-hairpin. The two protonatable residues of SH protein, His-22 and His-51, are located in the TM domain (lumenally oriented), and at the tip of the extramembrane C-terminal β hairpin (far from the channel pore), respectively. In a bicellar environment, however, the TM α-helix  extends up to His-51, and both His residues are accessible to the lumen of the channel²⁴. The channel structure adopts a  funnel-like architecture ²², where the narrower region (Ser-29 to Cys-45) ²² is lined with hydrophobic side chains (Ile-32, Ile-36, Ile-40 and Leu-44), and Ile-36 defines the narrowest point in the channel lumen. His-22 is located at the largest opening of this funnel, whereas His-51 is at the tip of the smallest opening.

In the present paper, analytical centrifugation in a sedimentation equilibrium mode has been used to determine if His protonation affects the stability of the SH protein pentamer. In this case, SH protein was solubilized in C14-betaine detergent, which has been used previously to show that SH protein forms pentameric oligomers²².

Protokół

This protocol is based on the following resources, which are to be referred for more details and special considerations^3,25-28.

1. Density matching of detergent micelles with ²H₂O

Note: The density of the buffer solution needs to be matched to the density of the detergent micelles. Common density-adjusting agents include ²H₂O, H₂¹⁸O, ²H₂¹⁸O, glycerol and sucrose²⁹. H₂¹⁸O has the same density as ²H₂O and may be a better choice if deuteration of exchangeable protons in the protein is not desired. In this procedure, the density of 3-(N,N-dimethylmyristylammonio)-propanesulfonate (C14SB) detergent in 50 mM Tris pH 7.3, 100 mM NaCl will be matched with ²H₂O. As an initial guess the following concentrations of ²H₂O will be used: 10, 30, and 50% v/v.

1.1. Sample preparation

1. Prepare the following stock solutions and filter sterilize through a 0.2 μm syringe filter: 50 mL 500 mM Tris pH 7.3 and 1 M NaCl (10X buffer solution); 1 mL 250 mM C14SB (50X detergent solution).
2. Prepare 200 μl of sample solution by mixing 20 μl 10X buffer solution, 4 μl 50X detergent solution, 20 μl ²H₂O (99.9%), and 156 μl deionized H₂O. Prepare also 200 μl of reference solution by mixing 20 μl 10X buffer solution, 20 μl ²H₂O (99.9%), and 160 μl deionized H₂O.
3. Repeat step 1.1.2 for the other ²H₂O concentrations, i.e. 30% and 50%, adjusting the ²H₂O and H₂O amounts appropriately.

1.2. Assembly of 6-channel AUC cells and sample loading into the cells.

Note: There are two types of AUC cell depending on the sample loading method. Cells without external fill has to be loaded prior to sealing the cell, whereas external-fill cells can be loaded after the cells are sealed. Assembly of an external-fill AUC cell has been described previously³. In this protocol, the assembly of a 6-channel AUC cell without external fill is described. The main difference is that it has screw rings on both sides which need to be tightened separately, and it doesn’t need housing plugs (Fig. 1). The difference in assembly steps are highlighted below.

Figure 1. Exploded view of a 6-channel AUC cell without external fill. This figure has been modified from Beckman Coulter An-50 Ti and An-60 Ti Analytical Rotor, Cells, and Counterbalance user manual.

1. Prepare two window assemblies for each AUC cell with sapphire window instead of quartz window (Fig. 2). Place the window gasket into the window holder. Slightly bend the window liner and place it into the window holder such that the gap is formed opposite to the window holder keyway. Place the sapphire window inside the window liner, aligning the mark with the window holder keyway.
   Note: The quartz window is compressible and thus will produce more light refraction at high speed ^{28, 30}. Therefore for interference measurements above 30000 rpm, such as in this density matching experiment, sapphire windows are used. A sapphire window is heavier than quartz window and has an “X” etched onto its side.

Figure 2. Exploded view of the window assembly. This figure has been modified from Beckman Coulter An-50 Ti and An-60 Ti Analytical Rotor, Cells, and Counterbalance user manual

1. Place the cell housing with the part number upside-down. With the keyways aligned with the housing key, slide into the cell housing firstly a 6-sector centerpiece with beveled side down, followed by one window assembly with the window facing down (Fig. 1, left).
2. Lightly coat the screw ring threads and screw ring washer with spinkote. Place a screw ring washer on top of the window assembly. Install the screw ring into the window housing with the word “OUT” facing outside. Hand-tighten the screw ring by using the cell aligning tool.
3. Using the torque wrench, tighten the screw ring to only 60 inch-pounds.
4. Place the cell with the part number upright and positioned at 12-noon. Load 120 μl reference into the left rows and 110 μl sample into the right rows. Ensure that each sample and reference is correctly paired.
   Note: Exact sample volume is not critical, but the reference needs to have slightly more volume than the sample (5-10 μl) so that the sample meniscus will be distinct.
5. Carefully slide into the cell housing one window assembly with the window facing down (Fig. 1, right). Take care not to disturb the cell excessively and spill the contents.
6. Repeat step 1.2.3 and 1.2.4, tightening the second screw ring to 120 inch-pounds. Invert the cell and re-tighten the first screw ring to 120 inch-pounds.
7. Load the cells into the rotor, install the rotor into the centrifuge and install the monochromator according to the manufacturer’s instructions ²⁸.
   Note: Details on this step can also be found in this reference ³.

1.3. Setting up interference measurement

1. Start up the user interface software for the AUC instrument and perform laser setup and radial calibration for each cell at 3000 rpm, according to the manufacturer’s instructions, which will be briefly summarized in the following step.
2. 1.3.1.1 After sufficient vacuum has been reached (< 100 microns), run the centrifuge at 3000 rpm. Preview the interference pattern in the user interface software and adjust the laser parameters to obtain the highest contrast.
3. Create a new set up file (File | New File) specifying “Equilibrium” and “Interference” measurement. Set up a sedimentation equilibrium method (“Method” button) to run at 45000 rpm or the highest speed anticipated for protein samples, whichever is higher, with run temperature at 20°C and collect 1 scan every 15 minutes. Monitor equilibrium progress by opening the data files in HeteroAnalysis and selecting “Match” function after at least 12 hours (approximately overnight, Fig. 3).
   Note: a similar function is also available in SEDFIT (Options | Loading Options | Test Approach to Equilibrium).

Figure 3. Result from HeteroAnalysis Match function. The Match function can be used to monitor equilibrium progress by comparing RMSD between successive scans and the last scan. This example shows attainment of equilibrium after 8 hr as indicated by RMSD values asymptotic to X-axis.

1.4. Data analysis

1. For each set of samples, plot the slope of the radial distribution profile against the ²H₂O concentration.
   Note: The distribution will be a very shallow exponential that approaches linearity. X-axis intercept corresponds to the matching ²H₂O concentration.
2. For more accurate results, perform the experiment in several replicates. Alternatively, repeat the experiment with a narrower range of ²H₂O concentration.

2. Sedimentation equilibrium of SH in C14SB micelles

2.1. Run parameters

1. Calculate buffer density and viscosity, protein partial specific volume and centrifugation speed by using SEDNTERP. To calculate buffer density and viscosity, select Compute in “Buffer Data Select” section and enter the buffer components accordingly, including the D₂O concentration.
2. 2.1.1.1 To calculate protein partial specific volume, select Compute in “V-bar” section and enter the protein amino acid sequence. Specify the highest expected oligomeric size in “Make an oligomer from this monomer: N=” field, in this case N = 5. Calculate the speed by entering values in the RPM field on the main window until σ ≈ 1; this is a rule of thumb to ensure a good exponential shape of the radial distribution profile²⁵.
   Note: The values calculated for this experiment was as follows: ρ = 1.03839 g/ml, η = 1.0267 cP = 0.7569 ml/g, ω₁ = 16000 rpm.
3. Calculate subsequent speeds to follow to ensure sufficient difference between the distribution profile at one speed and the next²⁵.
   Note: this can also be done from the function "Estimate equilibrium rotor speeds function" in SEDFIT, which takes into account the solution column (filling volume).

2.2. Sample preparations

1. Prepare 1 ml reference solution with 5 mM C14SB and 32.3% ²H₂O as determined from density matching experiment (section 1), by mixing 100 μl 10X buffer solution (step 1.1.1), 20 μl 50X detergent solution (step 1.1.1), 323 μl ²H₂O (99.9%) and 527 μl deionized H₂O.
2. Dissolve lyophilized, HPLC-purified SH peptides (expression and purification described previously³¹) in appropriate solvent such as methanol or 50% v/v aqueous acetonitrile. Measure A280 of the dissolved peptides in a microlitre-scale UV/Vis spectrophotometer and aliquot for three samples to give A_{280, 12mm} = 0.3, 0.5, and 0.8 (A_{280, 10mm} = 0.25, 0.417, and 0.67) each when diluted to 130 μl. Lyophilize the samples overnight and resuspend in 130 μl reference solution (step 2.2.1) to give the sample solutions.
   Note: SH protein can be detected from UV/Vis absorbance at 280 nm because it contains Trp and Tyr residues. Proteins without aromatic residues can be detected by tagging them with a suitable chromophore, using a Trp-containing mutant, or by using interference measurements instead of absorbance.
3. Follow steps in section 1.2 to assemble a 6-channel AUC cell with quartz windows. Load the highest concentration sample (A_{280, 12mm} = 0.8) in the channel nearest to the rotor center and lowest concentration sample (A_{280, 12mm} = 0.3) furthest from the rotor center.

2.3. Setting up absorbance measurements

1. Create a new set up file (File | New File) specifying “Equilibrium” and “Absorbance” measurement. Specify 280 nm as the detector wavelength.
2. Perform radial calibration at 3000 rpm by checking “Radial calibration before first scan” in Scan Options, specifying data collection at low resolution, e.g. with Radial step size = 0.01 cm, Replicates = 3 (low resolution, fast), and executing a Single Scan. After the scan is completed, uncheck the option.
3. Set up a sedimentation equilibrium method (“Method” button) to run at the first speed calculated in step 2.1.3, at 20°C, and collect 1 scan every 30 minutes. In each cells’ “Detail”, specify data collection at low resolution as in step 2.3.2. Monitor equilibrium progress by opening the data files in HeteroAnalysis and selecting “Match” function after at least 18 hours (approximately overnight, Fig. 4).
   Note: attainment of equilibrium may take substantially longer time for the first speed, whereas subsequent speeds will take less time.

Figure 4. Results from HeteroAnalysis Match function. The first and second speeds (top left and right) appear to have reached equilibrium, but it is better to wait a few more hours to be sure. In comparison, the third and fourth speeds (bottom left and right) have clearly reached equilibrium in a shorter time. Please click here to view a larger version of this figure.

1. Once equilibrium has been reached, collect a single scan at high resolution, e.g. with Radial step size = 0.001 cm, Replicates = 10 (high resolution, slow).
2. After the scan is completed, repeat step 2.3.3 and 2.3.4 for the next speed.
3. Optionally, when the time required to reach equilibrium for each speed is known (calculated or from experience), set up the sedimentation equilibrium method scan to include all the speeds calculated in step 2.1.3 and to collect 1 scan after the equilibration time for each speed. In this case, specify high resolution data collection in each cells’ “Detail”.

2.4. Data analysis in SEDFIT and SEDPHAT

Note: For further details and considerations in data analysis reader is referred to the following website: www.analyticalultracentrifugation.com.

1. Open high resolution scans in SEDFIT (Data | load sedimentation equilibrium data) and split the data into 3 channels (these correspond to different concentrations for each sample; Options | Loading Options |Save 6-channel Raw Data in 3 Subsets).
2. Re-open data files that belong to the same sample and same concentration but different speeds in SEDFIT. Adjust the meniscus (vertical red line), cell bottom (vertical blue line) and fitting limits (vertical green lines), and export the data for use in SEDPHAT (Data | Export Data to SEDPHAT). Input the parameters calculated in step 2.1.1, as well as rotor type and centerpiece type as requested. Repeat this step for every sample and concentration.
3. Open all data from the same sample (all concentrations and speeds) in SEDPHAT and fill in Experiment Parameters; an example is shown in Fig. 5.
   Note: when D₂O is added in the buffer, deuteration of exchangeable protons could significantly alter the molecular weight of the protein, especially for water-soluble proteins. Membrane proteins, especially small ones like SH protein, are less affected because membrane-embedded regions are protected from exchange. To correct this, input the “buffer D mol fraction”.
   Note: At this step it is recommended to save the edited dataset separately by selecting menu Data | Copy All Data And Save As New Config.
4. Select a Model and fill in Global Parameters for that model.
   Note: As an example, the “Monomer-n-Mer Self-Association” model and its parameters are shown in Fig. 6.

Figure 5. An example on how to fill in Experimental Parameters.

Figure 6. An example on how to fill in Global Parameters for Monomer-n-Mer Self-Association model.

1. Run a Global Fit by selecting menu Fit | Global Fit and wait until the fit converges. Note down (or take a screenshot of) the fitting results, especially the global reduced chi-square and log K_a values. Extract other data such as fit data and fitting residuals from menu Copy and Display | Display Thermodynamic Information.
2. Return to Global Parameters and check M(1) to fit the monomer molecular weight and repeat step 2.4.5. Note down the fitted molecular weight and global reduced chi-square.
3. Repeat step 2.4.3 to 2.4.6 for each model to be tested and compare the fit quality of each model by comparing the reduced global chi-square value as well as fitting residuals.
   Note: Small and random fitting residuals generally indicates a good fit, and the model that fits best would have the smallest global reduced chi-square. The fitted monomer molecular weight and its chi-square value should not differ substantially from that of the fixed (theoretical) molecular weight.
4. Calculate the confidence interval for the obtained log Ka by value by first selecting Statistics | Critical chi-square for error surface projections and inputting the desired confidence interval. Next, go to Statistics | Generate 1-dimensional error surface projection and unselect log Ka in Global Parameters dialog to obtain the chi-square values for log Ka.
   Note: readers are advised to consult the following sources (http://www.analyticalultracentrifugation.com/ sedphat/statistics.htm) for more details on the method ³² as well as illustration of this method ³³.

Wyniki

The radial distribution profile of C14SB detergent micelles in 50 mM Tris, 100 mM NaCl pH 7.3 forms a very shallow exponential that could be fitted to a linear model (Figure 7A). The slope of this distribution is inversely correlated to D₂O concentration (Figure 7B). The point where the slope is zero, i.e., the matching D₂O concentration, was found to be 32.3%.

See Figure 7 Below.

Dyskusje

This paper provides an experimental protocol for sample preparation and analysis of oligomerization of a small membrane protein in detergent using equilibrium sedimentation. The protocol described is equally valid –and simpler- for soluble proteins, as the density matching step is not required. Indeed, the system is constituted by a mixture of detergent and protein. To conduct sedimentation studies, the detergent must be invisible to the gravitational field so that it does not contribute to the particle flotation. ...

Materiały

Name	Company	Catalog Number	Comments
3-(N,N-dimethylmyristylammonio)propanesulfonate	Sigma	T0807
Deuterium oxide 99.8%	Cambridge Isotope	DLM-4-99.8
An-50 Ti Rotor, Analytical, 8-Place	Beckman Coulter	363782
An-60 Ti Rotor, Analytical, 4-Place	Beckman Coulter	361964
Cell housing	Beckman Coulter	334784
12 mm six-channel centerpiece, epon charcoal-filled	Beckman Coulter	331376
Window holder	Beckman Coulter	305037
Window gasket	Beckman Coulter	327021
Window liner	Beckman Coulter	362329
Sapphire window	Beckman Coulter	307177
Quartz window	Beckman Coulter	301730
Screw-ring washer	Beckman Coulter	362328
Screw ring	Beckman Coulter	301922
Spinkote	Beckman Coulter	306812
Torque stand assembly	Beckman Coulter	361318
Counterbalance	Beckman Coulter	360219
Cell alignment tool	Beckman Coulter	362340
SEDNTERP			http://bitcwiki.sr.unh.edu/index.php/Main_Page
HeteroAnalysis			http://www.biotech.uconn.edu/auf/?i=aufftp
SEDFIT			http://www.analyticalultracentrifugation .com/sedfit.htm
SEDPHAT			http://www.analyticalultracentrifugation .com/sedphat/default.htm