Fluorescence correlation methods for imaging cellular behavior of sphingolipid-interacting probes.

作者: Rachel Kraut , Nirmalya Bag , Thorsten Wohland

DOI: 10.1016/B978-0-12-386487-1.00018-3

关键词: CellBiologyDocking (molecular)Cell biologyFluorescenceCell signalingSphingolipidCell surface receptorMembraneFluorescence correlation spectroscopy

摘要: For cell biologists interested in the properties of membranes, their composition, and dynamics, realization that sphingolipids cholesterol have capacity to self-organize into ordered domains has given rise a need visualize these lipids actual living membranes. In order find out how various classes distribute membrane what behaviors are, it is extremely useful apply fluorescent probes either interact with lipids, or themselves behave like naturally occurring lipids. At same time, imaging modalities observe require appropriate spatial temporal resolution, on milli- microsecond timescale. Knowledge organization changes during processes signaling invasion by pathogens will undoubtedly be relevant our understanding action infectious diseases, bacterial toxins, even disease pathologies prion Alzheimer's disease, where glycosphingolipids (GSL) sphingolipid-rich act as receptors docking sites. such cases, composition dynamics clearly play role infectivity. The present challenge coming up high-resolution non-invasive approaches observing dynamic structural features sphingolipid-containing domains. This chapter discuss several variants applications fluorescence correlation spectroscopy well can used study sphingolipid dynamics.

参考文章(117)
F.M. Platt, G.R. Neises, R.A. Dwek, T.D. Butters, N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis. Journal of Biological Chemistry. ,vol. 269, pp. 8362- 8365 ,(1994) , 10.1016/S0021-9258(17)37202-2
A H Merrill, G van Echten, E Wang, K Sandhoff, Fumonisin B1 inhibits sphingosine (sphinganine) N-acyltransferase and de novo sphingolipid biosynthesis in cultured neurons in situ. Journal of Biological Chemistry. ,vol. 268, pp. 27299- 27306 ,(1993) , 10.1016/S0021-9258(19)74249-5
Single Molecules and Nanotechnology Single Molecules and Nanotechnology. ,vol. 12, ,(2008) , 10.1007/978-3-540-73924-1
Daniel Axelrod, Total internal reflection fluorescence microscopy in cell biology. Methods in Enzymology. ,vol. 361, pp. 1- 33 ,(2003) , 10.1016/S0076-6879(03)61003-7
Rhoderick E. Brown, Sphingolipid organization in biomembranes: what physical studies of model membranes reveal. Journal of Cell Science. ,vol. 111, pp. 1- 9 ,(1998) , 10.1242/JCS.111.1.1
N.O. Petersen, P.L. Höddelius, P.W. Wiseman, O. Seger, K.E. Magnusson, Quantitation of membrane receptor distributions by image correlation spectroscopy: concept and application Biophysical Journal. ,vol. 65, pp. 1135- 1146 ,(1993) , 10.1016/S0006-3495(93)81173-1
Akihiro Kusumi, Yuki M. Shirai, Ikuko Koyama-Honda, Kenichi G.N. Suzuki, Takahiro K. Fujiwara, Hierarchical organization of the plasma membrane: Investigations by single-molecule tracking vs. fluorescence correlation spectroscopy FEBS Letters. ,vol. 584, pp. 1814- 1823 ,(2010) , 10.1016/J.FEBSLET.2010.02.047
Radhia Mahfoud, Nicolas Garmy, Marc Maresca, Nouara Yahi, Antoine Puigserver, Jacques Fantini, Identification of a Common Sphingolipid-binding Domain in Alzheimer, Prion, and HIV-1 Proteins Journal of Biological Chemistry. ,vol. 277, pp. 11292- 11296 ,(2002) , 10.1074/JBC.M111679200