Time-resolved FTIR spectroscopy for monitoring protein dynamics exemplified by functional studies of Ras protein bound to a lipid bilayer
- 作者：Carsten Kö ; tting ; carsten.koetting@rub.de ; Jö ; rn Gü ; ldenhaupt ; Klaus Gerwert ; gerwert@bph.rub.de
- 关键词：Infrared ; Time-resolved ; Difference spectroscopy ; Rapid scan ; Step scan ; GTPases ; GTP ; Caged-substances ; Ras ; Isotopic labeling ; Band assignment ; Global fit ; Attenuated total reflection (ATR) ; Monolayer ; Solid supported lipid bilayer (SSLB)
- 刊名：Chemical Physics
- 出版年：2012
- 期刊代码：18_03010104
- 类别：ch
- 出版时间：2 March, 2012
- 卷：396
- 期：Complete
- 页码：72-83
- 文件大小：1899 K
摘要
Time-resolved Fourier transform infrared (FTIR) difference spectroscopy is a valuable tool for monitoring the dynamics of protein reactions and interactions. Absorbance changes can be monitored with time resolutions down to nanoseconds and followed for time periods that range over nine orders of magnitude. Membrane proteins bound to solid supported lipid bilayers can be investigated in near physiological conditions with the attenuated total reflection (ATR) technique. Here, we review the basics of time-resolved FTIR with a focus on Ras, a GTPase that is mutated in 25%of human tumors. We show the first time-resolved measurements of membrane anchored Ras and observed the switching between its activated and its inactivated state. We compared those measurements with measurements of the truncated Ras in solution. We found that both the kinetics and the functional groups involved were very similar. This suggested that the membrane did not have a major influence on the hydrolysis reaction.