CESI-MS of Intact Proteins

Transcription

1 CESI-MS of Intact Proteins Rob Haselberg, Chitra K. Ratnayake, Gerhardus J. de Jong, Govert W. Somsen. iomolecular nalysis, Utrecht University, Universiteitsweg 99, 58 CG, The Netherlands. eckman Coulter, Inc., 5 S. Kraemer lvd, M/S C.NW.5, rea, C 98, United States Introduction There is a growing need for selective and sensitive analytical tools for the characterization of intact proteins. The effective coupling of capillary electrophoresis and electrospray ionization timeof-fl ight mass spectrometry (CE-ESI-TOF-MS) may offer an attractive option by providing both the separation and detection required to distinguish structurally-related protein species [,]. In order to bring CE-ESI-MS to a high performance level, novel sheathless CE-MS interfacing was studied to achieve sensitive detection of intact proteins. stainless-steel capillary fused-silica wall polyimide { CE capillary electrical contact static conductive liquid feed CE capillary conductive liquid spray tip XYZstage nanospray endplate porous tip (length, ~ cm; wall thickness, 5 μm) MS inlet ased on a design of Moini [], a Particle Characterization prototype CESI sprayer was recently developed in the laboratories of eckman Coulter, Inc. Flow rates in CE are very low and the initial droplets formed during the sheathless electrospray process are small, which leads to more effi cient ionization (i.e., nanospray). With sheathless [] interfacing, the ESI [] spray tip can be positioned close to the MS inlet, thereby improving ion sampling effi ciencies. Overall, this can lead to enhanced sensitivity and lower limitsof-detection (LODs). The CESI sprayer provides electrical contact without the need for metal conductive coating, microelectrodes or liquid junctions. In the CESI design (Figure ), the last - cm of the bare fused-silica capillary are etched with hydrofl uoric acid until the section becomes conductive, producing an ~5-μm thick porous wall, which is conductive when in contact with an electrolyte. Capillaries with porous tips are simply inserted in a stainless steel ESI needle fi lled with a static conductive liquid. In this study, the performance of the CESI-MS of intact proteins was evaluated using some model proteins. Reproducibility, linearity and LODs were established. It is demonstrated that CESI-MS provides enhanced responses for intact proteins resulting in sub-nm detection limits. This is a 5- to -fold improvement compared to conventional sheath-liquid CE-MS interfacing using the same capillary dimensions. lood anking Capillary Electrophoresis Centrifugation Flow Cytometry Genomics Lab utomation Lab Tools Figure. () Detailed representation of the CESI sprayer design. () Schematic representation of the CESI-MS set-up using the porous tip. I-579

2 Materials and Methods Chemicals cetic acid (99.8%), ammonium hydroxide (5%) and isopropanol (IP) were obtained from Merck. Insulin (bovine pancreas), carbonic anhydrase II (bovine erythrocytes), ribonuclease (bovine pancreas) and lysozyme (chicken egg white) were from Sigma-ldrich. Protein test mixtures were prepared in the appropriate concentration with deionized water. GE of mm acetic acid (ph.) containing 5% IP was prepared by diluting.7 ml glacial acetic acid to ml with deionized water/ip (95/5, v/v) and adjusting the ph with ammonium hydroxide. CE system Experiments were carried out on a eckman Coulter capillary electrophoresis instrument. The separation voltage was - kv and the capillary temperature was C. Fused-silica capillaries (total length, cm; inner diameter, μm, outer diameter, 5 μm) equipped with the porous tip [] (length, - cm) were supplied by eckman Coulter. The capillaries were precoated with polyethylenimine (PEI). t the beginning of each day, the coated capillary was conditioned by fl ushing the capillary at 5 psi with air ( min), methanol ( min), deionized water (5 min) and GE ( min). efore each run, the capillary was fl ushed for min (5 psi) with fresh GE. The sample was injected for s at 5 psi. CE-MS MS detection was performed using a ruker Daltonics microtof orthogonal-accelerated time-of-fl ight (TOF) mass spectrometer. Sheathless CE-MS The capillary with the porous tip was placed in a grounded stainless steel needle that could be positioned by an XYZstage (eckman Coulter) fi tting the ruker microtof instrument (Figure ). nanospray end plate and gas diverter were installed to allow nanoesi. The porous tip protruded the grounded needle approximately.5 cm and the needle was fi lled with GE to establish the electrical contact. The optimized spray conditions were as follows; dry gas temperature, 8 C; dry gas nitrogen fl ow,. L/min; nebulizer pressure,. bar. Electrospray in positive ionization mode was achieved using an ESI voltage of -. kv. Sheath-liquid CE-MS For sheath-liquid interfacing, the capillary with porous tip was placed in a grounded coaxial CE-MS sprayer (gilent Technologies) installed on a conventional ESI source comprising the standard ESI endplate and capillary cap. fl ow of μl/min of IP-water-acetic acid (75:5:., v/v/v) was applied as sheath liquid. The optimized conditions for sheathliquid interfacing were: dry gas temperature, 8 C; dry gas nitrogen fl ow, L/min; nebulizer pressure,. bar; ESI voltage, -. kv. Data analysis CESI-MS data were analyzed using ruker Daltonics Data nalysis software. ase-peak electropherograms (PE) were constructed in the range m/z -. For determination of detection linearity and LOD, extracted-ion electropherograms (EIE) for the four model proteins were constructed from their most abundant m/z signals. These were m/z 7.7 and. for insulin, m/z., 6.9,., 8. and 5. for carbonic anhydrase II, m/z 5., 7. and for ribonuclease, and m/z.6, 59. and 789. for lysozyme. Results and Discussion The porous tip capillary was placed in a grounded needle that was positioned on an XYZ-stage (Figure ). The electrical contact was established by fi lling the stainless steel needle with GE. The liquid hardly evaporated from the needle and the same liquid could be used for an entire day of measurements. The porous tip capillaries were coated with positively-charged PEI, which exhibits a net positive charge when an acidic GE is used. Under these conditions, adsorption of peptides and proteins to the capillary wall will generally be avoided due to electrostatic repulsion. Most stable electrospray formation and highest analyte signals were obtained with the capillary tip at a distance of mm to the MS inlet.

3 intensity (x cnts) m/z Figure. () PE obtained with sheathless CESI-MS of a mixture of insulin (), carbonic anhydrase II (), ribonuclease () and lysozyme () (each 5 μg/ml). () Mass spectra obtained at the apices of peaks -. Further conditions, see Materials and Methods Section. mixture of insulin, carbonic anhydrase II, ribonuclease and lysozyme was analyzed by sheathless CESI-MS. Using a GE of mm acetic acid (ph.) with 5% IP, the four proteins were baseline separated within min (Figure ). IP was added to the GE as it provided a modest gain in protein signal intensities. Good quality mass spectra were obtained under these conditions (Figure ). Deconvolution of the mass spectra yielded masses of 57.6 Da (insulin), 9.6 Da (carbonic anhydrase II), 68.8 Da (ribonuclease ) and.5 Da (lysozyme), respectively, which agreed well with their expected molecular masses. The overall performance of the sheathless CESI-MS system was further evaluated by assessing the repeatability, detection linearity and LODs for the test proteins. Migration time RSDs for all four proteins were less than.8% (n=5) and peak area RSDs were within 8% (n=5). Plate numbers ranged from.5 x 5 (insulin) up to.5 x 5 (ribonuclease ). Clearly, the CESI-MS system allows repeatable and effi cient analyses of intact proteins. To check for detection linearity, protein mixtures with concentrations between.5 and 5 μg/ml of each protein were prepared and each solution was analyzed in triplicate. For all proteins, good linear relationships (Table ) between injected concentration and obtained peak areas were obtained. Table also lists the LODs (S/N=) achieved with sheathless CESI-MS. Sub-nM levels could still be detected for carbonic anhydrase II, ribonuclease and lysozyme indicating very favorable LODs for CESI-MS of intact proteins. sheathless interface c sheath liquid interface d protein R LOD R LOD insulin carbonic anhydrase II ribonuclease lysozyme Table. Linearity (R ) a and LODs (nm) b for the four model proteins obtained with CESI-MS and CE-MS with sheathliquid interfacing. a. Concentration range,.5-5 μg/ml (CESI-MS) and - μg/ml (sheath liquid). b. Concentration to yield S/N ratio of as calculated by extrapolation from -μg/ml injection. For carbonic anhydrase analyzed with sheath-liquid CE-MS, a 5-μg/mL injection was used. c. GE, mm ammonium acetate (ph.) containing 5% (v/v) isopropanol. d. GE, mm ammonium acetate (ph.).

4 In order to assess the gain in signal provided by CESI-MS, a comparison with sheath-liquid CE-MS was made. The same capillary, i.e. equipped with the porous tip, was placed in a coaxial sprayer installed on a conventional ESI source. sheath liquid of IP-water-acetic acid (75/5/., v/v/v) was applied at a fl ow rate of μl/min. These conditions had shown to be optimal for intact protein analysis in a previous CE-MS study []. baseline separation within min (Figure ) and linear protein signals (Table ) were obtained for the test proteins, indicating the proper functioning of the sheath-liquid interfacing. intensity (x cnts) Figure. PE obtained with sheath-liquid CE-MS of a mixture of insulin (), carbonic anhydrase II (), ribonuclease () and lysozyme () (each 5 μg/ml) using a conventional ESI source and a sheath liquid of isopropanol-water-acetic acid (75/5/., v/v/v). Further conditions, see Materials and Methods Section. Protein signals obtained with sheath liquid interfacing were approximately a factor to 5 lower with respect to CESI-MS (cf. fi gures and ; note that injected protein concentrations are 5 and 5 μg/ml, respectively). In particular, insulin showed reduced response with sheath liquid CE-MS. The lower protein signals are the overall result of the dilution of the CE effl uent by the sheath liquid and the lower ionization and ion sampling effi ciencies obtained using conventional ESI in stead of nanospray. It should be noted that the IP in the sheath liquid strongly enhances protein ionization, as without IP, protein signals are even much lower. Furthermore, the baseline noise observed is more favorable in CESI-MS (Figure ). intensity (cnts) Figure. aseline signal and noise in the min interval during () CESI-MS and () sheath-liquid CE-MS of the protein test mixture. Traces represent extracted-ion traces for insulin (; m/z.), carbonic anhydrase II (; m/z 6.9), ribonuclease (; m/z 7.) and lysozyme (; m/z/ 59.). Further conditions, see Materials and Methods Section. The application of sheath liquid causes signifi cant chemical noise, which is avoided with CESI-MS. Overall, the LODs achieved with CESI-MS are considerably lower than for sheath-liquid CE-MS (Table ).

5 Conclusion The performance of CESI-MS for the analysis of intact proteins was evaluated. Sub-nanomolar LODs were obtained with the CESI-MS system using a nanoesi source. These are highly favorable sensitivities which, to our knowledge, have not been achieved before with CE-MS for intact proteins. The gain in performance of the CESI-MS system with respect to sheath-liquid CE-MS can be attributed to the reduced noise levels and increased analyte responses. The very favorable LODs and overall performance indicates that CESI-MS can be highly useful for intact protein analysis. This article is based on results previously published in Journal of Chromatography (, vol. 7, pp ). References [] R. Haselberg, G.J. de Jong, G.W. Somsen, J. Chomatogr., 59 (7) 8. [] R. Haselberg, G.J. de Jong, G.W. Somsen, Electrophoresis, () 66. [] M. Moini, nal. Chem. 79 (7). [] R. Haselberg, G.J. de Jong, G.W. Somsen, nal. Chim cta, 678 () 8. In development. For Laboratory Use Only; not for use in diagnostic procedures. eckman Coulter and the stylized logo are trademarks of eckman Coulter, Inc., and are registered with the USPTO. For eckman Coulter s worldwide offi ce locations and phone numbers, please visit Contact Us at eckman Coulter, Inc. PRINTED IN U.S..