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http://www.lipidprofiles.com/ |
Markus
R WENK
(Associate Professor)
Contact Information:
Markus R. Wenk, PhD
National University of Singapore
Department of Biochemistry
8 Medical Drive, Block MD 7
Singapore 117597
T
+65 (6516) 3624
F +65 (6779) 1453
email: bchmrw@nus.edu.sg
Joint appointment : Department of Biochemistry and Department
of Biological Sciences |
Research Interest
Cellular membranes share common classes of lipid constituents,
but differ in the relative proportions of the individual
molecular species. They segregate cellular compartments and
provide a structural scaffold for the organization of enzymatic
machineries and for the anchoring of the cytoskeleton. In
addition, membrane lipids play an important role in cellular
signaling. This signaling function is made possible by the
very active metabolism of some lipids leading to the transient
accumulation of compounds that play critical roles in short
and long range cellular regulation. A well-known example
of regulatory phospholipids are the phosphoinositides (phosphorylated
derivatives of phosphatidylinositol) which contribute to
the regulation of nearly every cellular function including
membrane traffic, cell proliferation, and cell motility.
Similar signaling functions are emerging for a number of
other lipid classes, including ceramides, lysolipids, and
diacylglycerols.
The critical role of lipids in cell, tissue and organismal physiology
is demonstrated by a large number of genetic studies and by the
many human diseases involving the disruption of lipid metabolic
enzymes and pathways. Examples of such diseases include cancer,
diabetes and neurodegenerative diseases. Surprisingly, so far,
the explosion of information in the fields of genomics and proteomics
has not been matched by a corresponding advancement of knowledge
in the field of lipids. Conventional methods of lipid analysis
are hampered by low sensitivity and the difficulty to detect and
measure lipids from unprocessed extracts. Furthermore, many available
techniques of lipid analysis have not been suited to systematic
studies. We plan to capitalize on the increased sensitivity and
resolution power of mass spectrometry to advance the field and
obtain biologically and medically important information.
Enlarge
The inositol head group of phosphatidylinositol
can be reversibly phosphorylated at various positions resulting
in seven naturally occurring phosphoinositides. Shown here
is the molecular structure of 1-stearoyl-2-arachidonoyl-sn-glycero-3-phosphatidylinositol-4,5-bisphosphate,
an abundant PI(4,5)P2 species in mammalian cells. Commonly
used methods for the detection of phosphoinositides include
fluorescent techniques, receptor displacement assays and radiometric
measurements of chromatographically separated products after
metabolic labeling with radioisotope precursors. As a result,
some of these approaches report the position of the phosphate(s)
on the inositol headgroup (isomer information). Electrospray
ionization mass spectrometry, on the other hand, reveals a
number of PIP2 species with different fatty acid compositions,
depending on the number of carbon atoms and double bonds in
their fatty acid moieties. This fatty acid information adds
an additional layer of information to phosphoinositide signaling.
The dotted line indicates the plane of the bilayer and roughly
marks the aqueous-to-hydrophobic boundary of the membrane.
Current Projects
'Lipidomics of neuronal membranes - Identification of lipids involved
in neurosecretion and neurodegenerative diseases'
The goal of this project is to identify membrane lipids which
undergo stimulation induced metabolism during neurosecretion.
This work will be done in collaboration with research groups at
the National University of Singapore, the University of Western
Australia, Perth and Yale University in New Haven, CT, USA.
'Lipid profiling of Mycobacteria in
different physiological states'
The aim of this project is to test whether tubercle bacilli change
their membrane lipid composition upon entry into metabolically
inert states which are resistant to conventional anti-tuberculosis
treatment. Research collaboration with the Novartis Institute
for Tropical Diseases, Singapore.
'Lipidomics of enveloped viruses - novel
molecular insights into host-pathogen interactions'
Mass spectrometry will be used to determine the lipid inventory
of enveloped viruses which will be the first systematic high resolution
compositional analysis of viral envelope lipids. In collaboration
with groups at the Institute for Molecular and Cell Biology, Singapore
and Yale University, New Haven, CT, USA.
Selected Publications
-
Wenk
MR, Lucast L, Di Paolo G, Romanelli AJ, Suchy SF, Nussbaum RL,
Cline GW, Shulman GI, McMurray W, and P De Camilli. 2003. Nat.
Biotechnol. 7:813-817.
Phosphoinositide profiling in complex lipid mixtures using electrospray
ionization mass spectrometry.
-
Wenk
MR, and P De Camilli. 2003. Methods Enzymol.
372:248-260.
Assembly of endocytosis-associated proteins on liposomes.
-
Di
Paolo G, Pellegrini L, Letinic K, Cestra G, Zoncu R, Voronov
S, Chang S, Guo J, Wenk MR, and P De Camilli. 2002. Nature.
402:85-89.
PIP2 generation at sites of focal adhesion: Critical role for
the interaction of PIP Kinase I-gamma with the FERM domain of
talin.
-
Lee
E, Marcucci M, Daniell L, Pypaert M, Weisz O, Ochoa GC, Farsad
K, Wenk MR, and P De Camilli. 2002. Science.
297:1193-1197.
Amphiphysin 2 (Bin1) and T-tubule biogenesis in muscle.
-
Wenk
MR, Pellegrini L, Klenchin VA, Di Paolo G, Chang S, Daniell
L, Arioka M, Martin TF, and P De Camilli. 2001. Neuron
32:79-88.
PIP kinase I-gamma is the major PI(4,5)P2 synthesizing enzyme
at the synapse.
-
Cremona
O, Di Paolo G, Wenk MR, Luthi A, Kim WT, Takei K, Daniell L,
Nemoto Y, Shears SB, Flavell R, McCormick DA, and P De Camilli.
1999. Cell 99:179-188.
Essential role of phosphoinositide metabolism in synaptic vesicle
recycling.
-
Wenk
MR, and J Seelig. 1998. Biochim. Biophys. Acta
1372:2227-2236.
Proton induced vesicle fusion and the isothermal Lalpha<-HII
phase transition of lipid bilayers. A 31P-NMR and titration
calorimetry study.
-
Wenk
MR, and J Seelig. 1998. Biochemistry 37:3909-3916.
Magainin 2 amide interaction with lipid membranes: calorimetric
detection of peptide binding and pore formation.
-
Wenk
MR, and J Seelig. 1997. J. Phys. Chem. B 101:5224-5231.
Vesicle-micelle transformation of phosphatidylcholine / octyl-beta-D-glucopyranoside
mixtures as detected with titration calorimetry.
updated Aug 2007 |
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