Bremer, A.; Kent, B.; Hauß, T.; Thalhammer, A.; Yepuri, N.; Darwish, T.; Garvey, C.; Bryant, G.; Hincha, D.: Intrinsically Disordered Stress Protein COR15A Resides at the Membrane Surface during Dehydration. Biophysical Journal 113 (2017), p. 572-579
10.1016/j.bpj.2017.06.027
Open Access Version (externer Anbieter)
Abstract:
Plants from temperate climate zones are able to increase their freezing tolerance during exposure to low, above- zero temperatures in a process termed cold acclimation. During this process, several cold-regulated (COR) proteins are accu- mulated in the cells. One of them is COR15A, a small, intrinsically disordered protein that contributes to leaf freezing tolerance by stabilizing cellular membranes. The isolated protein folds into amphipathic a-helices in response to increased crowding condi- tions, such as high concentrations of glycerol. Although there is evidence for direct COR15A-membrane interactions, the orien- tation and depth of protein insertion were unknown. In addition, although folding due to high osmolyte concentrations had been established, the folding response of the protein under conditions of gradual dehydration had not been investigated. Here we show, using Fourier transform infrared spectroscopy, that COR15A starts to fold into a-helices already under mild dehydration conditions (97% relative humidity (RH), corresponding to freezing at 3 C) and that folding gradually increases with decreasing RH. Neutron diffraction experiments at 97 and 75% RH established that the presence of COR15A had no significant influence on the structure of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) membranes. However, using deuterated POPC we could clearly establish that COR15A interacts with the membranes and penetrates below the headgroup region into the upper part of the fatty acyl chain region. This localization is in agreement with our hypothesis that COR15A-membrane interaction is at least, in part, driven by a hydrophobic interaction between the lipids and the hydrophobic face of the amphipathic protein a-helix.