Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Tracking SNARE Complex Formation in Live Endocrine Cells
Seong J. An and
Wolfhard Almers*
Syntaxin, synaptosome-associated protein of 25 kD (SNAP25),and vesicle-associated membrane protein/synaptobrevin are collectivelycalled SNAP receptor (SNARE) proteins, and they catalyze neuronalexocytosis by forming a "core complex." The steps in core complexformation are unknown. Here, we monitored SNARE complex formationin vivo with the use of a fluorescent version of SNAP25. InPC12 cells, we found evidence for a syntaxin-SNAP25 complexthat formed with high affinity, required only the amino-terminalSNARE motif of SNAP25, tolerated a mutation that blocks formationof other syntaxin-SNAP25 complexes, and assembled reversiblywhen Ca2+ entered cells during depolarization. The complex mayrepresent a precursor to the core complex formed during a Ca2+-dependentpriming step of exocytosis.
Vollum Institute L-474, Oregon Health Sciences University, 3181 Southwest Sam Jackson Park Road, Portland, OR 97201, USA.
* To whom correspondence should be addressed. E-mail: almersw{at}ohsu.edu
Imaging and Nanomedicine for Diagnosis and Therapy in the Central Nervous System: Report of the Eleventh Annual Blood-Brain Barrier Disruption Consortium Meeting.
L.L. Muldoon, P.G. Tratnyek, P.M. Jacobs, N.D. Doolittle, G.A. Christoforidis, J.A. Frank, M. Lindau, P.R. Lockman, S.P. Manninger, Y. Qiang, et al. (2006)
AJNR Am. J. Neuroradiol.
27, 715-721
|Abstract »|Full Text »|PDF »
Conserved Prefusion Protein Assembly in Regulated Exocytosis.
C. Rickman, J. L Jimenez, M. E. Graham, D. A. Archer, M. Soloviev, R. D. Burgoyne, and B. Davletov (2006)
Mol. Biol. Cell
17, 283-294
|Abstract »|Full Text »|PDF »
Alternative Splicing of SNAP-25 Regulates Secretion through Nonconservative Substitutions in the SNARE Domain.
G. Nagy, I. Milosevic, D. Fasshauer, E. M. Muller, B. L. de Groot, T. Lang, M. C. Wilson, and J. B. Sorensen (2005)
Mol. Biol. Cell
16, 5675-5685
|Abstract »|Full Text »|PDF »
Electrochemical imaging of fusion pore openings by electrochemical detector arrays.
I. Hafez, K. Kisler, K. Berberian, G. Dernick, V. Valero, M. G. Yong, H. G. Craighead, and M. Lindau (2005)
PNAS
102, 13879-13884
|Abstract »|Full Text »|PDF »
Functions of SNAREs in intracellular membrane fusion and lipid bilayer mixing.
Dsl1p, Tip20p, and the Novel Dsl3(Sec39) Protein Are Required for the Stability of the Q/t-SNARE Complex at the Endoplasmic Reticulum in Yeast.
B. A. Kraynack, A. Chan, E. Rosenthal, M. Essid, B. Umansky, M. G. Waters, and H. D. Schmitt (2005)
Mol. Biol. Cell
16, 3963-3977
|Abstract »|Full Text »|PDF »
Endothelin-induced, Long Lasting, and Ca2+ Influx-independent Blockade of Intrinsic Secretion in Pituitary Cells by Gz Subunits.
S. A. Andric, D. Zivadinovic, A. E. Gonzalez-Iglesias, A. Lachowicz, M. Tomic, and S. S. Stojilkovic (2005)
J. Biol. Chem.
280, 26896-26903
|Abstract »|Full Text »|PDF »