High-Fidelity Protein Targeting into Membrane Lipid Microdomains in Living Cells

被引:21
作者
Beutel, Oliver [1 ]
Nikolaus, Joerg [2 ]
Birkholz, Oliver [1 ]
You, Changjiang [1 ]
Schmidt, Thomas [3 ]
Herrmann, Andreas [2 ]
Piehler, Jacob [1 ]
机构
[1] Univ Osnabruck, Div Biophys, Dept Biol, D-49076 Osnabruck, Germany
[2] Humboldt Univ, Inst Biol Biophys, D-10099 Berlin, Germany
[3] Leiden Inst Phys, Leiden, Netherlands
关键词
lipid-phase separation; lipid rafts; multivalent chelators; proteins; single-molecule studies; HISTIDINE-TAGGED PROTEINS; PLASMA-MEMBRANE; ANCHORED PROTEIN; T-CELLS; RAFT; DOMAINS; ORGANIZATION; RECOGNITION; SEGREGATION; COMPLEXES;
D O I
10.1002/anie.201306328
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lipid analogues carrying three nitrilotriacetic acid (tris-NTA) head groups were developed for the selective targeting of His-tagged proteins into liquid ordered (l(o)) or liquid disordered (l(d)) lipid phases. Strong partitioning into the l(o) phase of His-tagged proteins bound to tris-NTA conjugated to saturated alkyl chains (tris-NTA DODA) was achieved, while tris-NTA conjugated to an unsaturated alkyl chain (tris-NTA SOA) predominantly resided in the l(d) phase. Interestingly, His-tag-mediated lipid crosslinking turned out to be required for efficient targeting into the l(o) phase by tris-NTA DODA. Robust partitioning into l(o) phases was confirmed by using viral lipid mixtures and giant plasma membrane vesicles. Moreover, efficient protein targeting into l(o) and l(d) domains within the plasma membrane of living cells was demonstrated by single-molecule tracking, thus establishing a highly generic approach for exploring lipid microdomains in situ.
引用
收藏
页码:1311 / 1315
页数:5
相关论文
共 34 条
[1]   The HIV lipidome:: A raft with an unusual composition [J].
Brügger, B ;
Glass, B ;
Haberkant, P ;
Leibrecht, I ;
Wieland, FT ;
Kräusslich, HG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (08) :2641-2646
[2]   In vitro reconstitution of the ordered assembly of the endosomal sorting complex required for transport at membrane-bound HIV-1 Gag clusters [J].
Carlson, Lars-Anders ;
Hurley, James H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (42) :16928-16933
[3]   Membrane rafting: From apical sorting to phase segregation [J].
Coskun, Unal ;
Simons, Kai .
FEBS LETTERS, 2010, 584 (09) :1685-1693
[4]   Dimerization controls the lipid raft partitioning of uPAR/CD87 and regulates its biological functions [J].
Cunningham, O ;
Andolfo, A ;
Santovito, ML ;
Iuzzolino, L ;
Blasi, F ;
Sidenius, N .
EMBO JOURNAL, 2003, 22 (22) :5994-6003
[5]   Molecular recognition of histidine-tagged molecules by metal-chelating lipids monitored by fluorescence energy transfer and correlation spectroscopy [J].
Dorn, IT ;
Neumaier, KR ;
Tampé, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (12) :2753-2763
[6]   Single-molecule microscopy reveals plasma membrane microdomains created by protein-protein networks that exclude or trap signaling molecules in T cells [J].
Douglass, AD ;
Vale, RD .
CELL, 2005, 121 (06) :937-950
[7]   Lateral ligand-receptor interactions on membranes probed by simultaneous fluorescence-interference detection [J].
Gavutis, M ;
Lata, S ;
Lamken, P ;
Müller, P ;
Piehler, J .
BIOPHYSICAL JOURNAL, 2005, 88 (06) :4289-4302
[8]   The coreceptor CD2 uses plasma membrane microdomains to transduce signals in T cells [J].
Kaizuka, Yoshihisa ;
Douglass, Adam D. ;
Vardhana, Santosh ;
Dustin, Michael L. ;
Vale, Ronald D. .
JOURNAL OF CELL BIOLOGY, 2009, 185 (03) :521-534
[9]   Segregation of sphingolipids and sterols during formation of secretory vesicles at the trans-Golgi network [J].
Klemm, Robin W. ;
Ejsing, Christer S. ;
Surma, Michal A. ;
Kaiser, Hermann-Josef ;
Gerl, Mathias J. ;
Sampaio, Julio L. ;
de Robillard, Quentin ;
Ferguson, Charles ;
Proszynski, Tomasz J. ;
Shevchenko, Andrej ;
Simons, Kai .
JOURNAL OF CELL BIOLOGY, 2009, 185 (04) :601-612
[10]   Membrane mechanisms for signal transduction: The coupling of the meso-scale raft domains to membrane-skeleton-induced compartments and dynamic protein complexes [J].
Kusumi, Akihiro ;
Fujiwara, Takahiro K. ;
Morone, Nobuhiro ;
Yoshida, Kenta J. ;
Chadda, Rahul ;
Xie, Min ;
Kasai, Rinshi S. ;
Suzuki, Kenichi G. N. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2012, 23 (02) :126-144