Dynamic structural biology at the protein membrane interface
| dc.contributor.author | Burke, John E. | |
| dc.date.accessioned | 2021-01-29T19:10:11Z | |
| dc.date.available | 2021-01-29T19:10:11Z | |
| dc.date.copyright | 2019 | en_US |
| dc.date.issued | 2019 | |
| dc.description.abstract | Since I started doing scientific research, I've been fascinated by the interplay of protein structure and dynamics and how they together mediate protein function. A particular area of interest has been in understanding the mechanistic basis of how lipid-signaling enzymes function on membrane surfaces. In this award lecture article, I will describe my laboratory's studies on the structure and dynamics of lipid-signaling enzymes on membrane surfaces. This is important, as many lipid-signaling enzymes are regulated through dynamic regulatory mechanisms that control their enzymatic activity. This article will discuss my continued enthusiasm in using a synergistic application of hydrogen–deuterium exchange MS (HDX–MS) with other structural biology techniques to probe the mechanistic basis for how membrane-localized signaling enzymes are regulated and how these approaches can be used to understand how they are misregulated in disease. I will discuss specific examples of how we have used HDX–MS to study phosphoinositide kinases and the protein kinase Akt. An important focus will be on a description of how HDX–MS can be used as a powerful tool to optimize the design of constructs for X-ray crystallography and EM. The use of a diverse toolbox of biophysical methods has revealed novel insight into the complex and varied regulatory networks that control the function of lipid-signaling enzymes and enabled unique insight into the mechanics of membrane recruitment. | en_US |
| dc.description.reviewstatus | Reviewed | en_US |
| dc.description.scholarlevel | Faculty | en_US |
| dc.identifier.citation | Burke, J. E. (2019). Dynamic structural biology at the protein membrane interface. Journal of Biological Chemistry, 294(11), 3872-3880. https://doi.org/10.1074/jbc.AW118.003236. | en_US |
| dc.identifier.uri | https://doi.org/10.1074/jbc.AW118.003236 | |
| dc.identifier.uri | http://hdl.handle.net/1828/12625 | |
| dc.language.iso | en | en_US |
| dc.publisher | Journal of Biological Chemistry | en_US |
| dc.subject | phosphoinositide | |
| dc.subject | hydrogen-deuterium exchange mass spectrometry | |
| dc.subject | HDX–MS | |
| dc.subject | phosphatidylinositol kinase | |
| dc.subject | Akt PKB | |
| dc.subject | protein dynamics | |
| dc.subject | PI3K | |
| dc.subject | PI4K | |
| dc.subject | PI3K/Ak | |
| dc.subject | Akt | |
| dc.subject | lipid signaling | |
| dc.subject | phosphatidylinositide 3-kinase (PI3K) | |
| dc.subject.department | Department of Biochemistry and Microbiology | |
| dc.title | Dynamic structural biology at the protein membrane interface | en_US |
| dc.type | Article | en_US |