On the Mechanism of Theta Capillary Nanoelectrospray Ionization for the Formation of Highly Charged Protein Ions Directly from Native Solutions.

Theta capillary nanoelectrospray ionization (θ-nanoESI) can be used to "supercharge" protein ions directly from solution for detection by mass spectrometry (MS). In native top-down MS, the extent of protein charging is low. Given that ions with more charge fragment more readily, increasing charge can enhance the extent of sequence information obtained by top-down MS. For θ-nanoESI, dual-channeled nanoESI emitters are used to mix two solutions in low to sub-μs prior to MS. The mechanism for θ-nanoESI mixing has been reported to primarily occur: (i) in a single shared Taylor cone and in the droplets formed from the Taylor cone or (ii) by the fusion of droplets formed from two separate Taylor cones. Using θ-nanoESI-ion mobility MS, native protein solutions were rapidly mixed with denaturing supercharging solutions to form protein ions in significantly higher charge states and with more elongated structures than those formed by premixing the solutions prior to nanoESI-MS. If θ-nanoESI mixing occurred in the Taylor cone and in the droplets resulting from the single Taylor cone, then the extent of protein charging and unfolding should be comparable to or less than that obtained by premixing solutions. Thus, these data are consistent with mixing occurring via droplet fusion rather than in the Taylor cone prior to ESI droplet formation. These data also suggest that highly charged protein ions can be formed by the near-complete mixing of each solution. The presence of supercharging additives in premixed solutions can suppress volatile electrolyte evaporation, limiting the extent of protein charging compared to when the additive is delivered via one channel of a θ-nanoESI emitter. In θ-nanoESI, the formation of two Taylor cones can presumably result in substantial electrolyte evaporation from the ESI droplets containing native-like proteins prior to droplet fusion, thereby enhancing ion charging.

[1]  N. Kelleher,et al.  The Human Proteoform Project: Defining the human proteome , 2021, Science advances.

[2]  M. Jarrold Applications of Charge Detection Mass Spectrometry in Molecular Biology and Biotechnology. , 2021, Chemical reviews.

[3]  W. Donald,et al.  Protein-Small Molecule Interactions in Native Mass Spectrometry. , 2021, Chemical reviews.

[4]  I. Kaltashov,et al.  Charge Manipulation Using Solution and Gas-Phase Chemistry to Facilitate Analysis of Highly Heterogeneous Protein Complexes in Native Mass Spectrometry. , 2021, Analytical chemistry.

[5]  Huilin Li,et al.  High-Pressure Electrospray Ionization Yields Supercharged Protein Complexes from Native Solutions while Preserving Noncovalent Interactions. , 2020, Analytical chemistry.

[6]  C. Supuran,et al.  Supercharging protein ions in native mass spectrometry using theta capillary nanoelectrospray ionization mass spectrometry and cyclic alkylcarbonates. , 2018, Analytica chimica acta.

[7]  Lars Konermann,et al.  Addressing a Common Misconception: Ammonium Acetate as Neutral pH “Buffer” for Native Electrospray Mass Spectrometry , 2017, Journal of The American Society for Mass Spectrometry.

[8]  M. Leeming,et al.  Highly Charged Protein Ions: The Strongest Organic Acids to Date. , 2017, Angewandte Chemie.

[9]  R. Zare,et al.  Rapid Hydrogen-Deuterium Exchange in Liquid Droplets. , 2017, Journal of the American Chemical Society.

[10]  J. Loo,et al.  Salt Bridge Rearrangement (SaBRe) Explains the Dissociation Behavior of Noncovalent Complexes , 2016, Journal of The American Society for Mass Spectrometry.

[11]  E. Williams,et al.  Ultrafast (1 μs) Mixing and Fast Protein Folding in Nanodrops Monitored by Mass Spectrometry. , 2016, Journal of the American Chemical Society.

[12]  C. Borchers,et al.  Protein species-specific characterization of conformational change induced by multisite phosphorylation. , 2016, Journal of proteomics.

[13]  E. Williams,et al.  Supercharging with m-nitrobenzyl alcohol and propylene carbonate: forming highly charged ions with extended, near-linear conformations. , 2015, Analytical chemistry.

[14]  E. Williams,et al.  Theta-Glass Capillaries in Electrospray Ionization: Rapid Mixing and Short Droplet Lifetimes , 2014, Analytical chemistry.

[15]  J. Loo,et al.  What Protein Charging (and Supercharging) Reveal about the Mechanism of Electrospray Ionization , 2014, Journal of The American Society for Mass Spectrometry.

[16]  C. Borchers,et al.  Top‐down mass spectrometry and hydrogen/deuterium exchange for comprehensive structural characterization of interferons: Implications for biosimilars , 2014, Proteomics.

[17]  W. Donald,et al.  Solution additives for supercharging proteins beyond the theoretical maximum proton-transfer limit in electrospray ionization mass spectrometry. , 2014, Analytical chemistry.

[18]  Christine M. Fisher,et al.  Affecting protein charge state distributions in nano-electrospray ionization via in-spray solution mixing using theta capillaries. , 2014, Analytical chemistry.

[19]  I. Kaltashov,et al.  Conformer-specific characterization of nonnative protein states using hydrogen exchange and top-down mass spectrometry , 2013, Proceedings of the National Academy of Sciences.

[20]  P. Derrick,et al.  Dual Nano-Electrospray for Probing Solution Interactions and Fast Reactions of Complex Biomolecules , 2012, European journal of mass spectrometry.

[21]  M. Gross,et al.  New Protein Footprinting: Fast Photochemical Iodination Combined with Top-Down and Bottom-Up Mass Spectrometry , 2012, Journal of The American Society for Mass Spectrometry.

[22]  E. Williams,et al.  Electrothermal supercharging of proteins in native electrospray ionization. , 2012, Analytical chemistry.

[23]  A. Burlingame,et al.  The role of conformational flexibility on protein supercharging in native electrospray ionization. , 2011, Physical chemistry chemical physics : PCCP.

[24]  J. Loo,et al.  Top-Down Mass Spectrometry of Supercharged Native Protein-Ligand Complexes. , 2011, International journal of mass spectrometry.

[25]  C. Robinson,et al.  Collision cross sections of proteins and their complexes: a calibration framework and database for gas-phase structural biology. , 2010, Analytical chemistry.

[26]  Christopher J. Hogan,et al.  Ion mobility-mass spectrometry of phosphorylase B ions generated with supercharging reagents but in charge-reducing buffer. , 2010, Physical chemistry chemical physics : PCCP.

[27]  E. Williams,et al.  Effects of supercharging reagents on noncovalent complex structure in electrospray ionization from aqueous solutions , 2010, Journal of the American Society for Mass Spectrometry.

[28]  J. Loo,et al.  New reagents for increasing ESI multiple charging of proteins and protein complexes , 2010, Journal of the American Society for Mass Spectrometry.

[29]  P. Kebarle,et al.  Electrospray: from ions in solution to ions in the gas phase, what we know now. , 2009, Mass spectrometry reviews.

[30]  Christoph H Borchers,et al.  Hydrogen/deuterium exchange mass spectrometry with top-down electron capture dissociation for characterizing structural transitions of a 17 kDa protein. , 2009, Journal of the American Chemical Society.

[31]  E. Williams,et al.  Origin of supercharging in electrospray ionization of noncovalent complexes from aqueous solution , 2009, Journal of the American Society for Mass Spectrometry.

[32]  J. Loo,et al.  Increasing charge while preserving noncovalent protein complexes for ESI-MS , 2009, Journal of the American Society for Mass Spectrometry.

[33]  J. Shabanowitz,et al.  Peptide and protein sequence analysis by electron transfer dissociation mass spectrometry. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[34]  C. Enke,et al.  Practical implications of some recent studies in electrospray ionization fundamentals. , 2001, Mass spectrometry reviews.

[35]  F. McLafferty,et al.  Electron capture dissociation for structural characterization of multiply charged protein cations. , 2000, Analytical chemistry.

[36]  Martin F. Jarrold,et al.  CONFORMATIONS, UNFOLDING, AND REFOLDING OF APOMYOGLOBIN IN VACUUM : AN ACTIVATION BARRIER FOR GAS-PHASE PROTEIN FOLDING , 1997 .

[37]  A. Shvartsburg,et al.  An exact hard-spheres scattering model for the mobilities of polyatomic ions , 1996 .

[38]  P. Schnier,et al.  On the maximum charge state and proton transfer reactivity of peptide and protein ions formed by electrospray ionization , 1995, Journal of the American Society for Mass Spectrometry.

[39]  M. Mann,et al.  Electrospray ionization for mass spectrometry of large biomolecules. , 1989, Science.