Using Empirical Phase Diagrams to Understand the Role of Intramolecular Dynamics in Immunoglobulin G Stability
dc.contributor.author | Ramsey, Joshua D. | |
dc.contributor.author | Gill, Michelle L. | |
dc.contributor.author | Kamerzell, Tim J. | |
dc.contributor.author | Price, E. Shane | |
dc.contributor.author | Joshi, Sangeeta B. | |
dc.contributor.author | Bishop, Steven M. | |
dc.contributor.author | Oliver, Cynthia N. | |
dc.contributor.author | Middaugh, C. Russell | |
dc.date.accessioned | 2017-04-26T19:34:04Z | |
dc.date.available | 2017-04-26T19:34:04Z | |
dc.date.issued | 2009-07 | |
dc.identifier.citation | Ramsey, J. D., Gill, M. L., Kamerzell, T. J., Price, E. S., Joshi, S. B., Bishop, S. M., … Middaugh, C. R. (2009). Using Empirical Phase Diagrams to Understand the Role of Intramolecular Dynamics in Immunoglobulin G Stability. Journal of Pharmaceutical Sciences, 98(7), 2432–2447. http://doi.org/10.1002/jps.21619 | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/23821 | |
dc.description.abstract | Understanding the relationship between protein dynamics and stability is of paramount importance to the fields of biology and pharmaceutics. Clarifying this relationship is complicated by the large amount of experimental data that must be generated and analyzed if motions that exist over the wide range of timescales are to be included. To address this issue, we propose an approach that utilizes a multidimensional vector-based empirical phase diagram (EPD) to analyze a set of dynamic results acquired across a temperature-pH perturbation plane. This approach is applied to a humanized immunoglobulin G1 (IgG1), a protein of major biological and pharmaceutical importance whose dynamic nature is linked to its multiple biological roles. Static and dynamic measurements are used to characterize the IgG and to construct both static and dynamic empirical phase diagrams. Between pH 5 and 8, a single, pH-dependent transition is observed that corresponds to thermal unfolding of the IgG. Under more acidic conditions, evidence exists for the formation of a more compact, aggregation resistant state of the immunoglobulin, known as A-form. The dynamics-based EPD presents a considerably more detailed pattern of apparent phase transitions over the temperature-pH plane. The utility and potential applications of this approach are discussed. | en_US |
dc.publisher | Elsevier | en_US |
dc.rights | This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | en_US |
dc.subject | Immunglobulin G. | en_US |
dc.subject | Molecular dynamics | en_US |
dc.subject | Physical characterization | en_US |
dc.subject | Physical stability | en_US |
dc.subject | Empirical phase diagram | en_US |
dc.title | Using Empirical Phase Diagrams to Understand the Role of Intramolecular Dynamics in Immunoglobulin G Stability | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Ramsey, Joshua D. | |
kusw.kuauthor | Gill, Michelle L. | |
kusw.kuauthor | Kamerzell, Tim J. | |
kusw.kuauthor | Price, E. Shane | |
kusw.kuauthor | Joshi, Sangeeta B. | |
kusw.kuauthor | Middaugh, C. Russell | |
kusw.kudepartment | Pharmaceutical Chemistry | en_US |
kusw.kudepartment | Chemistry | en_US |
dc.identifier.doi | 10.1002/jps.21619 | en_US |
kusw.oaversion | Scholarly/refereed, author accepted manuscript | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.identifier.pmid | PMC3762222 | en_US |
dc.rights.accessrights | openAccess |
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Except where otherwise noted, this item's license is described as: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.