Abstract
Membrane proteins are notoriously difficult to crystallise for use in X-ray crystallographic structural determination, or too complex for NMR structural studies. Circular dichroism (CD) is a fast and relatively easy spectroscopic technique to study protein conformational behaviour in solution. The advantage of synchrotron radiation circular dichroism (SRCD) measured with synchrotron beamlines compared to the CD from benchtop instruments is the extended spectral far-UV region that increases the accuracy of secondary structure estimations, in particular under high ionic strength conditions. Membrane proteins are often available in small quantities, and for this SRCD measured at the Diamond B23 beamline has successfully facilitated molecular recognition studies. This was done by probing the local tertiary structure of aromatic amino acid residues upon addition of chiral or non-chiral ligands using long pathlength cells (1–5 cm) of small volume capacity (70 μl–350 μl). In this chapter we describe the use of SRCD to qualitatively and quantitatively screen ligand binding interactions (exemplified by Sbma, Ace1 and FsrC proteins); to distinguish between functionally similar drugs that exhibit different mechanisms of action towards membrane proteins (exemplified by FsrC); and to identify suitable detergent conditions to observe membrane protein-ligand interactions using stabilised proteins (exemplified by inositol transporters) as well as the stability of membrane proteins (exemplified by GalP, Ace1). The importance of the in solution characterisation of the conformational behaviour and ligand binding properties of proteins in both far- andnear-UV regions and the use of high-throughput CD (HT-CD) using 96- and 384-well multiplates to study the folding effects in various protein crystallisation buffers are also discussed.
The original version of this chapter has been revised. An erratum to this chapter can be found at DOI 10.1007/978-3-319-35072-1_13
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Keywords
- Circular dichroism (CD)
- Synchrotron radiation circular dichroism (SRCD)
- Protein secondary structure
- Local tertiary structure
- High throughput-CD (HTCD)
- SRCD UV-denaturation assay
- Ligand binding
4.1 Introduction
Circular Dichroism (CD) and Synchrotron Radiation CD (SRCD) has been proven to be highly useful for studies of ligand binding by soluble proteins, particularly as it is a relatively quick and easy spectroscopic measurement, requiring no extensive sample preparation, and it has the potential to be used in high throughput (HT-CD) screening (Mason 1982; Fasman 1996; Berova et al. 2000, 2012; Siligardi and Hussain 1998, 2015; Siligardi et al. 2002; Martin et al. 2011; Johnson 1990; Kelly et al. 2005; Siligardi and Hussain 2010; Jávorfi et al. 2010; Fiedler et al. 2013).
CD spectroscopy has been widely used for the purposes of determining secondary structural content and integrity of membrane proteins (e.g. histidine kinases – Potter et al. 2002; Kim et al. 2010; Keegan et al. 2010; Yeo et al. 2008; membrane transporters – Psakis et al. 2009), protein fragments (e.g. Powl et al. 2010), and protein unfolding (Psakis et al. 2009; Keegan et al. 2010). Sreerama and Woody 2004, found that the CD analysis of secondary structure content of membrane proteins using soluble protein reference sets was slightly inferior to that obtained for soluble proteins. The inclusion of membrane proteins in the soluble protein reference sets – now a common practise – has since improved the CD analysis for both membrane and soluble proteins.
In the last few decades, drug discovery has benefited from information about the three-dimensional structure of proteins at atomic resolution determined by X-ray crystallography (Carvalho et al. 2009) and NMR spectroscopy (Pellecchia et al. 2008). However, the number of solved human protein structures deposited in the Protein Data Bank is still only a small fraction of the approximately 20,000 protein-coding genes in the human genome (Pennisi 2012). As many proteins that cannot be studied by either X-ray crystallography due to their failure to crystallise or by Nuclear magnetic resonance spectroscopy (NMR) due to their size or irregular structure, can be characterized in terms of protein folding by CD, which is the differential absorption between left and right circularly polarized light (Fasman 1996), see Fig. 4.1. CD spectroscopy is sensitive to the absolute configuration and conformation of chiral molecules. With the exception of glycine, amino acids are chiral molecules adopting either L or D stereo-isomers which are non-superimposable mirror-imaged configurations. Natural proteins only consist of L amino acids.
The application of CD spectroscopy for ligand binding studies of membrane proteins has proved more limited, largely due to the technical challenges associated with working with hydrophobic membrane proteins. The use of the B23 beamline (Diamond Light Source synchrotron) for SRCD has overcome the limitations encountered in studying precious membrane proteins often available in very small quantities. The B23 beamline has enabled the use of small volume capacity cuvette cells for the measurements in the far-UV and near-UV spectral regions that could not otherwise be used with bench-top CD instruments. The UV protein denaturation assay, a unique feature of the B23 beamline, is another method developed to assess ligand binding interactions, in particular for achiral fatty acid ligand analogues or small organic molecules devoid of UV chromophores, which are difficult, if not impossible to investigate with bench-top CD instruments. The higher vacuum UV and far-UV photon flux has proved essential for the spectroscopic characterisation of membrane proteins in high salt concentrations to enhance protein stability, which cannot be achieved satisfactorily with bench-top instruments due to absorption cut-off.
In this chapter, several examples of SRCD spectroscopy applied to the study of membrane proteins in solution using the Diamond B23 beamline (Hussain et al. 2012a, b; Jávorfi et al. 2010) are presented. Qualitative and quantitative assessments of ligand binding interactions of the FsrC, SbmA, and Ace1 membrane proteins, identification of functionally similar but mechanistically distinct drug targeting FsrC, and the characterisation of suitable detergent conditions for ligand-membrane proteins interaction studies are reviewed.
4.2 Diamond B23 Beamline for Synchrotron Radiation Circular Dichroism (SRCD)
The B23 beamline is a bending magnet beamline at Diamond Light Source, UK, dedicated to SRCDspectroscopy. The beamline consists of two distinct end-stations: module A in operation since 2011 and module B in operation since 2009, see Fig. 4.1. The beamline operates in the wavelength range of 125–650 nm, delivering a highly collimated beam with a focal spot size at the sample of 0.5 mm2 and a photon flux in excess of 1012 photons/s. The high brilliance of the beamline, coupled with its highly collimated incident micro-beam is enabling a large variety of measurements and experiments to be carried out, ranging from dilute to highly concentrated solutions, to thin solid films. The end-station of module A operates in the wavelength range of 125–500 nm and is primarily dedicated to the study of thin chiral films, whereas module B operating in the 165–650 nm is dedicated to solutions and liquid samples. A novel vertical sample chamber, which is unique among the other SRCD beamlines around the world, has been developed to accommodate a horizontal X-Y motorised stage that can hold either the temperature controlled stage (such as Linkam™ stage), which can operate in cryogenic and high temperature conditions (from −150 °C to 300 °C), or standard microtiter or microwell plates (96- and 384-well Suprasil quartz plates (Siligardi and Hussain 2015) for high throughput CD (HT-CD) screening.
Module B is dedicated to ligand binding interactions that are often carried out as CD titrations using small aperture cuvette cells that require the ability to optimise beam alignment in a fast and reproducible manner using a manual X-Y stage (Borisenko et al. 2015). This allows for measurements of dilute solutions (as low as 5 nM protein concentration) (Laera et al. 2011) using small volume capacity cells such as 0.800 ml for 10 cm pathlength or 0.020 ml for 1 cm pathlength. SRCD stopped-flow can also be carried out in both modules. The higher photon flux of SRCD beamlines has traditionally been considered detrimental as it promotes protein denaturation. Measures have been put in place to eliminate or greatly reduce this effect, however, this phenomenon, has also been exploited at the B23 beamline as UV protein denaturation (Hussain et al. 2012a, b; Jávorfi et al. 2010) can be conveniently used to measure accelerated protein photo stability as a function of protein formulation and qualitatively assessing and screening ligand binding interactions (Hussain et al. 2012a, b; Longo et al. 2014, 2015). For module B, a rotating sample cell holder has also been introduced to eliminate protein denaturation induced by the higher vacuum UV and far-UV photon flux for experiments where the UV denaturation effect is not desirable, such as thermal denaturation. Finally, to support the capabilities and potential of B23 beamline applications, a concerted software development program has been put in place. Users can now reduce and analyse their data through a single software application developed at the beamline – CDApps (Hussain et al. 2015). The software is available for users on-site, as well as via remote access, and allows novice users to quickly process their data and take full advantage of the technique.
4.3 Ligand Binding Studies of the FsrC, Ace1 and SbmA Membrane Proteins
Protein-ligand binding interactions can be assessed by a variety of techniques such as Isothermal Calorimetry (ITC) , Surface Plasmon Resonance (SPR), Fluorescence and Circular Dichroism (CD) . Each technique has its own strengths and weaknesses. ITC can often be inconclusive when the thermal effects associated with the displacement of the bound solvent molecules by the ligand are rather small. SPR requires one of the components to be immobilized, which can lead to false positive or false negative results when compared to non-immobilized conditions. Fluorescence requires the presence of a fluorophore that does not absorb and emit light at the same wavelength for the ligand and/or protein (Tryptophan and Tyrosine residues). CD relies on detectable spectral differences between the observed spectrum of the protein-ligand mixture at (x:y) molar ratio and the calculated sum of the spectra of the protein at (x) molar ratio and ligand at (y) molar ratio. For achiral ligands, the comparison is facilitated by the fact that the ligand chromophore will acquire an induced CD upon binding of a protein site that is chiral. In this case, the detection of any induced CD, which is any spectral difference from that of the protein alone, is unambiguously indicative of the presence of a bound species, as the free achiral form is devoid of any CD from its UV absorbing chromophore (Siligardi and Hussain 1998; Hussain et al. 2012b; Siligardi et al. 2002; Martin et al. 2011). However, for ligands with weak or with no UV chromophore groups, such as sugars, lipids and irregular peptides, the lack of any CD spectral change upon ligand addition does not necessarily signify that there are no binding interactions. The ligand might bind far from the aromatic side-chains of the protein, without causing any detectable secondary structure conformational change. For these cases, the protein UV denaturation assay using the B23 beamline was developed and is now part of the facilities available at the Diamond B23 beamline (Hussain et al. 2012a, b; Jávorfi et al. 2010). High UV photon flux at B23 was used to qualitatively distinguish the binding of ligands to proteins, such as non-steroidal anti-inflammatory drugs to serum albumin, though not a membrane protein is a transporter (Fig. 4.2) (Hussain et al. 2012a). UV denaturation can also be used to discriminate the effects of different excipients, such as detergents, salts, and buffers on peptide hormones such as vasoactive peptide VIP, which binds to a GPCR (Longo et al. 2015) and antibodies (such as cetuximab which is an inhibitor of EGFR, a transmembrane protein) on the effect of formulating agents (Longo et al. 2015; Siligardi and Hussain 2015). These measurements are easy to carry out, as it only requires repeated scanning of samples and a plot of the denaturation decay, which will provide differential dynamics properties of the system.
Binding studies using the CD titration method are even more challenging for membrane proteins than they are for soluble proteins. A common limitation encountered with membrane proteins is that they are often expressed in rather small quantities. At the B23 beamline, the highly collimated incident micro-beam (0.3 × 0.5 mm) is enabling the use of a small aperture cuvette cells of low volume capacity (from few μl to 25 μl for 0.01 cm to 1 cm pathlengths) to measure the SRCD of precious and scarce membrane proteins.
FsrC, a membrane protein histidine kinase, showed very little conformational changes in secondary structure upon addition of ligand Gelatinase Biosynthesis-Activating Pheromone (GBAP). However, the local tertiary structure of FsrC showed significant changes when GBAP was added, indicating the involvement of aromatic residues binding to GBAP, see Fig. 4.3. Qualitative studies showed that the affinity of the ligand GBAP to FsrC was 2 μM, monitored at a single wavelength of 277 nm. Further competitive binding studies with another ligand, siamycin I, showed that siamycin I did not compete with GBAP and that aromatic side-chain residues should be involved in the interaction with the ligand (Patching et al. 2012; Phillips-Jones et al. 2013).
SbmA, a bacterial inner membrane protein of Gram-negative bacteria is involved in the transport within the cell of prokaryotic and eukaryotic antimicrobial peptides and glycopeptides, as well as of peptide-nucleic acid (PNA) oligomers. A SbmA homolog, BacA, is required for the development of Sinorhizobium meliloti bacteroids within plant cells and favours chronic infections with Brucella abortus and Mycobacterium tuberculosis in mice. A SRCD spectroscopic study provided evidence that SbmA and BacA interact in vitro with Bac7 (1–35), a proline rich peptide. Bac7 was titrated at various molar ratios to SbmA and BacA in both the far-UV (180–260 nm) and near-UV (250–330 nm) regions. In the far-UV region, significant changes of secondary structure were observed upon addition of Bac7 to SbmA (see Fig. 4.4a and Table 4.1) and BacA (Fig. 4.4b) indicating binding interactions. In the near-UV region (Runti et al. 2013), characteristic of the local tertiary structure of aromatic side-chain residues (Tryptophan, Tyrosine and Phenylalanine) (Siligardi et al. 1991; Siligardi and Hussain 1998; Hussain et al. 2012b; Gaspar et al. 2011) no significant changes were observed, which suggests that no aromatic residues were involved at close range (radius of 6 Å) in the interface between ligand and protein. The SRCD spectra were converted to ΔA = (AL−AR) units from millidegree units and the plot of ΔA intensities at 223 nm versus the concentrations of Bac7 used in the titration was analysed with a non-linear regression method (Siligardi et al. 2002) to quantitatively determine the dissociation constant using CDApps software (Hussain et al. 2015). The results showed that the peptide had similarly high binding affinities to SbmA (Kd of 0.26 μM) and BacA (Kd of 0.3 μM).
For the membrane protein Ace1 (actinobacter chlorhexidine efflux transport system 1), no significant conformational changes in the far-UV region (180–250 nm) were observed in the presence of an achiral chlorhexidine antibacterial drug (Hassan et al. 2013). However, in the near-UV region, the SRCD titration unambiguously showed the induced CD of the bound chorhexidine to the AceI membrane protein (Fig. 4.5a). The non-linear regression analysis of the SRCD data revealed adissociation constant (Kd) of 6 μM (Fig. 4.5b). In this example the binding was demonstrated by the increased induced CD at about 270 nm, which reach a plateau upon saturation. The ligand binding did not perturb the content of the secondary structure of Ace1, as illustrated by the lack of conformational changes in the far-UVSRCD spectrum.
4.4 Protein Stability
Throughout the course of protein production, different batches of proteins are expressed and different protocols or procedures for purification are used. These variables can have an effect on the integrity of the proteins. This is especially relevant to membrane proteins that have to be solubilised in different detergents for stabilisation and for crystallisation with potential ligand molecules.
The example of the FsrC protein (Patching et al. 2012) showed that it required 1.5 h of incubation time for stabilisation, which was determined by measuring consecutive repeated scans of about 3 min each in the 260–180 nm region until the dominating alpha helical spectral feature stopped increasing at about 30 scans, see Fig. 4.6. It was essential to know the specific equilibration time for FsrC, and more generally, the equilibration time for membrane proteins in each specific detergent, when assessing ligand binding interactions, as otherwise it might result in ambiguous results. Interestingly, for FsrC the addition of ligand peptide GBAP appeared to stabilize the protein rather quickly (Fig. 4.6). The sugar transport protein GalP was also monitored for stability over time using the repeated scan method using high UV photon flux (Kalverda et al. 2014) showing that GalP is stable over repeated scans using a smaller bandwidth of 1.1 nm.
4.5 Temperature Denaturation
Temperature denaturation studies on proteins are routinely used to determine the thermodynamic properties of wild type proteins, their mutants, and the effect of ligand binding interactions or that of excipients as stabilisers to withstand long protein storage and transport conditions.
However, for the SbmA protein (described in Sect. 4.4) the thermal behaviour was not affected by the addition of peptide Bac-7 (Fig. 4.7a), even though conformational changes by SRCD were observed in the far-UV region (Fig. 4.4) (Runti et al. 2013). The SRCD titration of Bac7 with SbmA indicated that the molecular interaction was accompanied by an 11 % decrease in alpha helical content for either SbmA or Bac7 (Table 4.1). The thermal studies, however, showed no significant differences between the melting temperature (Tm = 55 °C) of SbmA and the melting temperature of a mixture of SbmA and Bac7 (Fig 4.7).
In the temperature denaturation study of the Ace1 protein (Kalverda et al. 2014) the protein melting temperatures were measured by ramping the temperature from 5 to 90 °C while monitoring the far-UVCD spectrum, particularly at 209 nm or 222 nm. The wild-type protein was observed to be rather stable at temperatures below 60 °C. However, mutant E50Q Ace1, known to impair resistance to chlorhexidine, showed thermal denaturation at 40 °C. Chlorhexidine binding greatly increased the thermal stability of the E50Q mutant protein in a dose-dependent manner. Importantly, these experiments yielded evidence, albeit indirect, that the Ace1 protein was itself involved in binding chlorhexidine as an integral feature of the resistance mechanism.
In a study by Bettaney et al. (2013), the SRCD spectra of three inositol membrane transport proteins (IolF, IolT, and YfiG) measured with the Diamond B23 beamline showed a cut-off below 180 nm, indicated by the voltage of the photomultiplier tube (PMT) detector exceeding 600 V (Fig. 4.8). It is essential for accurate secondary structure estimations that the positive CD bands at about 190–195 nm of the α-helical conformation are measured with the lowest level of noise possible, which can be readily achieved with synchrotron CD beamlines. Repeated scans can also improve the signal-to-noise-ratio, but at an increased overall time (the noise is reduced by the root square of the number of scans). Following successful confirmation of secondary structural integrity and composition, the specificity of IolF, IolT, and YfiG for a large variety of inositols and sugars of D and L configurationn was determined by measuring the cellular uptake of radiolabelled 3H-myo-inositol in the presence of unlabelled competing compounds (Bettaney et al. 2013) as well as differences in thermodynamic properties, which could give indications of any concerns for crystallisation trials.
4.6 Conformational Analysis and HT-CD Screening of Protein Crystallisation Buffers
The assessment of protein folding in solution is particularly important because conformational changes among a wild type protein and its mutants/constructs are likely to affect the protein activity and stability. Protein folding plays a crucial role in the function of a protein and its characterisation is a prerequisite for the understanding of the mechanism and consequences of sequence amino acid point mutation that could trigger protein misfolding for insulin, α-synuclein, lysozyme, and transthyrethin to name but a few cases with serious health implications (Blancas-Mejía and Ramirez-Alvarado. 2013; Ruzza et al. 2014, 2015; Marchiani et al. 2013).
A recent example regarding the importance of protein folding characterisation (including different constructs of the same protein) by SRCD is the case of the membrane protein GDP-mannose-dependent mannosyltransferase WbdD. In this example, the accurate determination of the α-helical content of the protein was crucial as a molecular ruler to regulate O-antigen chain length in lipopolysaccharide of E coli 09A (Hagelueken et al. 2015).
WbdD is a membrane-associated protein and its interaction with WbdA (another GDP-mannose-dependent mannosyltransferase) is essential for the ability of the soluble polymerase to act on the membrane-embedded undecaprenyl lipid–linked acceptor (Clarke et al. 2009). The authors investigated two insertion and two deletion variants of WbdD1–556 to gain some structural insight into the effect of the changes in the coiled-coil region. Multi-techniques such as the crystal structure of WbdD1-556 showing the coiled-coil region, molecular modelling and small angle X-ray scatterings (SAXS) models were coupled to elucidate the 3D structure. The study was further expanded with a bioassay of different constructs, giving various lengths of coupled lipopolysaccharides with CD spectroscopy. Circular dichroism analysis of WbdD1–459 and WbdD1–556 using the CONTINLL algorithm (Sreerama and Woody 2004; Hussain et al. 2015) on spectra collected on B23 at Diamond confirmed a detectable increase in α-helical content, as was expected by the addition of a coiled-coil region (Fig. 4.9). This multi-technique study helps to piece together information gathered and complements the limitations of each of the individual techniques into a final and more complete understanding of the role of the coiled-coil region of the protein as a molecular ruler.
The high photon flux of the B23 beamline has been successfully used to develop a protein UV-denaturation assay that can discriminate the relative stability of different types of protein folding and also to qualitatively determine ligand binding interactions (Hussain et al. 2012a, b; Jávorfi et al. 2010; Longo et al. 2014, 2015). The latter application has been very useful to study ligands with weak or no UV chromophores that would otherwise be difficult or impossible to monitor by conventional benchtop CD spectrometer.
The conformation of peptides and proteins is known to be affected by environmental conditions such as buffer composition, pH, salt concentration, detergents, metal ions and precipitants. The latter is widely used in crystallography to enhance crystallisation. However, the use of CD spectroscopy for such characterisations would be rather laborious and time consuming as this would normally be carried out by measuring the samples in a single cuvette cell, one by one. The unique highly collimated incident micro-beam (from 0.3 mm2 to 1.5 mm2 cross section) of the B23 has recently been exploited for the use of 96- or 384-well plates, to allow for high throughput CD (HT-CD) (Fig. 4.10) screening to characterise protein folding in crystallisation conditions and in protein-drug binding interactions (Siligardi and Hussain 2015).
Myoglobin, a highly α-helical protein, was investigated by SRCD spectroscopy dissolved in a selection of 48 conditions from the MemGold2 crystallisation screen (Molecular Dimensions) that is widely used for membrane protein crystallization. The corresponding 48 SRCD spectra (Fig. 4.11) showed significant conformational differences that could be attributed to electrolyte concentration and pH. It is important to note that despite myoglobin being a highly α-helical soluble protein its conformation can be perturbed by the membrane protein crystallisation buffer MemGold2. This can be readily illustrated in the pie chart of the secondary structure content determined by SRCD spectroscopy using CONTINLL of the SRCD spectra of the 96-well multiplate (Fig. 4.12).
Most membrane proteins are highly helical and it is not inconceivable that they too might behave similarly to myoglobin under various buffer conditions. This is consistent with the fact that membrane proteins only crystallise in certain buffer conditions (Privé 2007; O’Malley 2011) but not in others. This raises the question whether proteins that do not crystallise do not do so because they have different conformations that do not promote association or that their thermodynamic properties are significantly different, inhibiting crystal formation.
The availability of HT-CD facility at the B23 beamline opens up the possibility of finding cross-correlations between buffer conditions and protein conformation, identifying possible buffer targets that could promote crystallisation for further 3D structural determination by X-ray crystallography.
4.7 Conclusion
The work described in this chapter highlights the use of CD and SRCD spectroscopy for studies of membrane proteins, particularly when a wide spectral range from far-UV to near-UV region (180–350 nm) is achieved for both protein and ligand. This approach enables the determination of the stability and content of the protein secondary structure, the qualitative and quantitative assessment of ligand binding interactions and the characterisation of the solvent (detergent) conditions to optimise protein stability and binding properties. It has been successful in the identification of drugs that despite similar activity revealed different thermodynamics properties when bound to various protein constructs.
The amide bond of the protein backbone structure gives information about the protein secondary structure while the aromatic side-chains of the tryptophan, tyrosine and phenylalanine amino acid residues provide details about their local tertiary structure, as such, these are ideal as molecular probes for ligand binding interactions. The chromophore of the ligand can be used to unambiguously determine ligand binding in both far- and near-UV regions and in particular whether protein conformational changes are occurring upon ligand binding. Further development in high throughput allows the screening of crystallization buffers and the potential screening of ligands in drug discovery with membrane proteins acting as host or target receptor. This broad approach of CD spectroscopy in solution for membrane proteins is advantageous. SRCD in particular provides wavelength extension in the vacuum UV region and higher photon flux, which enables more penetrating measurements with less transparent media (NaCl content up to 500 mM) and in small volume capacity cuvette cells that are unattainable using bench-top CD instruments .
References
Berova N, Nakanichi K, Woody RW (2000) Circular dichroism principles and applications, 2nd ed. New York: Wiley-VCH
Berova N, Polavarapu PL, Nakanishi K, Woody RW (2012) Comprehensive chiroptical spectroscopy: applications in sterochemical analysis of synthetic compounds, natural products and biomolecules, vol 2. New Jersey: John Wiley & Sons
Bettaney KE, Sukumar P, Hussain R, Siligardi G, Henderson PJF, Patching SG (2013) A systematic approach to the amplified expression, functional characterization and purification of inositol transporters from Bacillus subtilis. Mol Membr Biol 30:3–14
Blancas-Mejía LM, Ramirez-Alvarado M (2013) Systemic amyloidoses. Annu Rev Biochem 82:745–774
Borisenko KB, Shanmugam J, Williams BAO, Ewart P, Gholipour B et al (2015) Photo-induced optical activity in phase-change memory materials. Sci Rep 5:8770
Carvalho AL, Trincão J, Romão MJ (2009) X-ray crystallography in drug discovery. Methods Mol Biol 572:31–56
Clarke BR, Greenfield LK, Bouwman C, Whitfield C (2009) Coordination of polymerisation, chain termination, and export in assembly of the Escherichia coli lipopolysaccharide 09a antigen in an ATP-binding cassette transporter-dependent pathway. J Biol Chem 284:30662–30672
Fasman GD (1996) Circular dichroism and the conformational analysis of biomolecules. Plenum Press, New York
Fiedler S, Cole L, Keller S (2013) Automated circular dichroism spectroscopy for medium-throughput analysis of protein conformation. Anal Chem 85:868–1872
Gaspar D, Lúcio M, Rocha S, Costa Lima JLF, Reis S (2011) Changes in PLA2 activity after interacting with anti-inflammatory drugs and model membranes: evidence for the involvement of tryptophan residues. Chem Phys Lipids 164:292–299
Hagelueken G, Clarke BR, Huang H, Tuukkanen A, Danciu I et al (2015) A coiled-coil domain acts as a molecular ruler to regulate O-antigen chain length in lipopolysaccharide. Nat Struct Mol Biol 22:50–56
Hassan KA, Jackson S, Penesyan A, Patching S, Tetu SG et al (2013) Transcriptomic and biochemical analyses identify a family of chlorhexidine efflux proteins. Proc Natl Acad Sci U S A 110(50):20254–20259
Hussain R, Jávorfi T, Siligardi G (2012a) Circular dichroism beamline B23 at the Diamond Light Source. J Synchrotron Radiat 19:32–135
Hussain R, Jávorfi T, Siligardi G (2012b) Spectroscopic analysis: synchrotron radiation circular dichroism. Comprehen Chiral 8:438–448
Hussain R, Benning K, Myatt D, Jávorfi T, Longo E et al (2015) CDApps: integrated software for experimental planning and data processing at beamline B23 Diamond Light Source. J Synchrotron Radiat 22:465–468
Jávorfi T, Hussain R, Myatt D, Siligardi G (2010) Measuring circular dichroism in a capillary cell using the B23 synchrotron radiation CD beamline at Diamond Light Source. Chirality 22:149–E153
Johnson WC (1990) Protein secondary structure and circular dichroism: a practical guide. Proteins: Struct Funct Bioinf 7:205–214
Kalverda AP, Gowdy J, Thompson GS, Homans SW, Henderson PJF, Patching S (2014) TROSY NMR with a 52 kDa sugar transport protein and the binding of a small-molecule inhibitor. Mol Membr Biol 31:131–140
Keegan N, Ridley H, Lakey JH (2010) Discovery of biphasic thermal unfolding of OmpC with implications for surface loop stability. Biochemistry 49:9715–9721
Kelly SM, Jess TJ, Price NC (2005) How to study proteins by circular dichroism. Biochim Biophys Acta 1751:119–139
Kim YP, Yeo KJ, Kim MH, KimY-C JYH (2010) Structural characterisation of the intra-membrane histidine kinase YbdK from Bacillus subtilis in DPC micelles. Biochem Biophys Res Commun 391:1506–1511
Laera S, Ceccone G, Rossi F, Gilliland D, Hussain R, Siligardi G, Calzolai L (2011) Measuring protein structure and stability of protein-nanoparticle systems with synchrotron radiation circular dichroism. Nano Lett 11:4480–4484
Longo E, De Santis E, Hussain R, van Der Walle C, Casas-finet J, Uddin S, dos Santos A, Siligardi G (2014) The effect of palmitoylation on the conformation and physical stability of a model peptide hormone. Int J Pharm 472:156–164
Longo E, Hussain R, Siligardi G (2015) Application of circular dichroism and magnetic circular dichroism for assessing biopharmaceuticals formulations photo-stability and small ligands binding properties. Int J Pharm 480:84–91
Marchiani A, Mammi S, Siligardi G, Hussain R, Tessari I, Bubacco L, Delogu G, Fabbri D, Dettori MA, Sanna D, Dedola S, Serra PA, Ruzza P (2013) Small molecules interacting with α-synuclein: antiaggregating and cytoprotective properties. Amino Acids 45:327–338
Martin SR, Schilstra MJ, Siligardi G (2011) Biophysical approaches determining ligand binding to biomolecular targets, detection, measurement and modelling. In: Podjarmy A, Dejaegere A, Kieffer B (eds) Chapter 7: circular dichroism. Cambridge: RSC Publishing, pp 226–246
Mason SF (1982) Molecular optical activity and the chiral discrimination. Cambridge University Press, Cambridge
O’Malley MA, Helgeson ME, Wagner NJ, Robinson AS (2011) Towards rational design of protein detergent complexes: determinants of mixed micelles that are critical for the in vitro stabilisation of a G-protein coupled receptor. Biophys J 101:1938–1948
Patching SG, Edara S, Ma P, Nakayama J, Hussain R, Siligardi G, Phillips-Jones MK (2012) Interactions of the intact FsrC membrane histidine kinase with its pheromone ligand GBAP revealed through synchrotron radiation circular dichroism. Biochim Biophys Acta Biomembr 1818:1595–1602
Pellecchia M, Bertini I, Cowburn D, Dalvit C, Giralt E et al (2008) Perspectives on NMR in drug discovery: a technique comes of age. Nat Rev Drug Discov 7:738–745
Pennisi E (2012) ENCODE project writes eulogy for junk DNA. Science 337:1159–1160
Phillips-Jones MK, Patching SG, Edara S, Nakayama J, Hussain R, Siligardi G (2013) Interactions of the intact FsrC membrane histidine kinase with the tricyclic peptide siamycin I revealed through synchrotron radiation circular dichroism. Phys Chem Chem Phys 15:444–447
Potter CA, Ward A, Lauri C, Williamson MP, Henderson PJF, Phillips-Jones MK (2002) Expression, purification and characterisation of full-length heterologously expressed histidine protein kinase RegB from Rhodobacter sphaeroides. J Mol Biol 320:201–213
Powl AM, O’Reilly AO, Miles AJ, Wallace BA (2010) Synchotron radiation circular dichroism spectroscopy-defined structure of the C-terminal domain of NaChBac and its role in channel assembly. Proc Natl Acad Sci U S A 107:14064–14069
Privé GG (2007) Detergents for the stabilization and crystallization of membrane proteins. Methods 41:388–397
Psakis G, Saidijam M, Shibayama K, Polaczek J, Bettaney KE et al (2009) The sodium-dependent D-glucose transport protein of Helicobacter pylori. Mol Microbiol 71:391–403
Runti G, del Carmen LRM, Stoilova T, Hussain R, Jennions M, Choudhury HG, Benincasa M, Gennaro R, Beis K, Scocchi M (2013) Functional characterization of SbmA, a bacterial inner membrane transporter required for importing the antimicrobial peptide Bac7(1-35). J Bacteriol 195:5343–5351
Ruzza P, Siligardi G, Hussain R, Marchiani A, Islami M et al (2014) Ceftriaxone blocks the polymerization of α-synuclein and exerts neuroprotective effects in vitro. ACS Chem Neurosci 5:30–38
Ruzza P, Hussain R, Biondi B, Calderan A, Tessari I, Bubacco L, Siligardi G (2015) Effects of trehalose on thermodynamic properties of alpha-synuclein revealed through synchrotron radiation circular dichroism. Biomolecules 5:724–734
Siligardi G, Hussain R (1998) Biomolecules interactions and competitions by non-immobilised ligand interaction assay by circular dichroism. Enantiomer 3:77–87
Siligardi G, Hussain R (2010) Applications of circular dichroism. In: Lindon J, Tranter G, Koppenaal D (eds) Encyclopedia of spectroscopy and spectrometry, vol 1, 2nd edn. Elsevier, Oxford, pp 9–14
Siligardi G, Hussain R (2015) CD spectroscopy: an essential tool for quality control of protein folding. In: Raymond JO (ed) Structural proteomics: high-throughput methods, methods in molecular biology, vol 1261. New York: Springer; pp 255–276
Siligardi G, Campbell MM, Gibbons WA, Drake AF (1991) Conformational analysis of the melanin concentrating hormone (MCM) by CD spectroscopy: disulphide bridge and aromatic tyrosyl contribution. Eur J Biochem 206:23–29
Siligardi G, Panaretou B, Meyer P, Singh S, Woolfson DN, Piper PW, Pearl LH, Prodromou C (2002) Regulation of Hsp90 ATPase activity by the co-chaperone Cdc37p/p50cdc37. J Biol Chem 277:20151–20159
Sreerama N, Woody RW (2004) On the analysis of membrane protein circular dichroism spectra. Protein Sci 13:100–112
Yeo KJ, Kwak S-N, Kim HJ, Cheong C, Kim MH, Jeon YH (2008) Expression and characterisation of the integral membrane domain of bacterial histidine kinase SCO3062 for structural studies. Biochem Biophys Res Commun 376:409–413
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We gratefully acknowledge the Diamond Light Source Ltd. for the B23 beamtime allocation (www.diamond.ac.uk/Home/ForUsers.html).
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Hussain, R., Siligardi, G. (2016). Characterisation of Conformational and Ligand Binding Properties of Membrane Proteins Using Synchrotron Radiation Circular Dichroism (SRCD). In: Moraes, I. (eds) The Next Generation in Membrane Protein Structure Determination. Advances in Experimental Medicine and Biology, vol 922. Springer, Cham. https://doi.org/10.1007/978-3-319-35072-1_4
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