The role of lipids and salts in two-dimensional crystallization of the glycine-betaine transporter BetP from Corynebacterium glutamicum

被引:12
|
作者
Tsai, Ching-Ju
Ejsing, Christer S.
Shevchenko, Andrej
Ziegler, Christine
机构
[1] Max Planck Inst Biophys, Dept Biol Struct, D-60438 Frankfurt, Germany
[2] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
关键词
membrane proteins; 2D crystallization; lipid species; mass spectroscopy; multiple-precursor ion scanning; electron microscopy;
D O I
10.1016/j.jsb.2007.09.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The osmoregulated and chill-sensitive glycine-betaine transporter (BetP) from Corynebacterium glutamicum was reconstituted into lipids to form two-dimensional (2D) crystals. The sensitivity of Bet? partly bases on its interaction with lipids. Here we demonstrate that lipids and salts influence crystal morphology and crystallinity of a C-terminally truncated BetP. The salt type and concentration during crystallization determined whether crystals grew in the form of planar-tubes, sheets or vesicles, while the lipid type influenced crystal packing and order. Three different lipid preparations for 2D crystallization were compared. Only the use of lipids extracted from C. glutamicum cells led to the formation of large, well-ordered crystalline areas. To understand the lipid-derived influence on crystallinity, lipid extracts from different stages of the crystallization process were analyzed by quantitative multiple-precursor ion scanning mass spectroscopy (MS). Results show that BetP has a preference for fatty acid moieties 16:0-18:1, and that a phosphatidyl glycerol (PG) 16:0-18:1 rich preparation prevents formation of pseudo crystals. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:275 / 286
页数:12
相关论文
共 5 条
  • [1] Regulative interactions of the osmosensing C-terminal domain in the trimeric glycine betaine transporter BetP from Corynebacterium glutamicum
    Kraemer, Reinhard
    Ziegler, Christine
    BIOLOGICAL CHEMISTRY, 2009, 390 (08) : 685 - 691
  • [2] Conformational changes of the betaine transporter BetP from Corynebacterium glutamicum studied by pulse EPR spectroscopy
    Nicklisch, S. C. T.
    Wunnicke, D.
    Borovykh, I. V.
    Morbach, S.
    Klare, J. P.
    Steinhoff, H. -J.
    Kraemer, R.
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2012, 1818 (03): : 359 - 366
  • [3] Regulatory Properties and Interaction of the C- and N-Terminal Domains of BetP, an Osmoregulated Betaine Transporter from Corynebacterium glutamicum
    Ott, Vera
    Koch, Joachim
    Spaete, Kira
    Morbach, Susanne
    Kraemer, Reinhard
    BIOCHEMISTRY, 2008, 47 (46) : 12208 - 12218
  • [4] Structure determination of secondary transport proteins by electron crystallography: Two-dimensional crystallization of the betaine uptake system BetP
    Tsai, CJ
    Ziegler, C
    JOURNAL OF MOLECULAR MICROBIOLOGY AND BIOTECHNOLOGY, 2005, 10 (2-4) : 197 - 207
  • [5] A role for native lipids in the stabilization and two-dimensional crystallization of the Escherichia coli NADH-ubiquinone oxidoreductase (complex I)
    Sazanov, LA
    Carroll, J
    Holt, P
    Toime, L
    Fearnley, IM
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (21) : 19483 - 19491