Literature DB >> 8785339

Immuno-atomic force microscopy of purple membrane.

D J Müller1, C A Schoenenberger, G Büldt, A Engel.   

Abstract

The atomic force microscope is a useful tool for imaging native biological structures at high resolution. In analogy to conventional immunolabeling techniques, we have used antibodies directed against the C-terminus of bacteriorhodopsin to distinguish the cytoplasmic and extracellular surface of purple membrane while imaging in buffer solution. At forces > or = 0.8 nN the antibodies were removed by the scanning stylus and the molecular topography of the cytoplasmic purple membrane surface was revealed. When the stylus was retracted, the scanned membrane area was relabeled with antibodies within 10 min. The extracellular surface of purple membrane was imaged at 0.7 nm resolution, exhibiting a major and a minor protrusion per bacteriorhodopsin monomer. As confirmed by immuno-dot blot analysis and sodium dodecyl sulfate-gel electrophoresis, labeling of the purple membrane was not observed if the C-terminus of bacteriorhodopsin was cleaved off by papain.

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Year:  1996        PMID: 8785339      PMCID: PMC1225149          DOI: 10.1016/S0006-3495(96)79743-6

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  32 in total

1.  Atomic force microscopy produces faithful high-resolution images of protein surfaces in an aqueous environment.

Authors:  S Karrasch; R Hegerl; J H Hoh; W Baumeister; A Engel
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2.  Scanning tunnelling microscopy observations of biomolecules on layered materials.

Authors:  H Jungblut; S A Campbell; M Giersig; D J Müller; H J Lewerenz
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Journal:  Biochemistry       Date:  1995-07-04       Impact factor: 3.162

5.  Bacteriorhodopsin precursor is processed in two steps.

Authors:  U Wölfer; N A Dencher; G Büldt; P Wrede
Journal:  Eur J Biochem       Date:  1988-05-16

6.  Topology of the morphological domains of the chaperonin GroEL visualized by immuno-electron microscopy.

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7.  The correlation averaging of a regularly arranged bacterial cell envelope protein.

Authors:  W O Saxton; W Baumeister
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8.  Model for the structure of bacteriorhodopsin based on high-resolution electron cryo-microscopy.

Authors:  R Henderson; J M Baldwin; T A Ceska; F Zemlin; E Beckmann; K H Downing
Journal:  J Mol Biol       Date:  1990-06-20       Impact factor: 5.469

9.  Localization of a sequence motif complementary to the nuclear localization signal in proteasomes from Thermoplasma acidophilum by immunoelectron microscopy.

Authors:  A Grziwa; B Dahlmann; Z Cejka; U Santarius; W Baumeister
Journal:  J Struct Biol       Date:  1992 Sep-Oct       Impact factor: 2.867

10.  Location of subunits within the acetylcholine receptor by electron image analysis of tubular crystals from Torpedo marmorata.

Authors:  E Kubalek; S Ralston; J Lindstrom; N Unwin
Journal:  J Cell Biol       Date:  1987-07       Impact factor: 10.539

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  13 in total

1.  Tapping-mode atomic force microscopy produces faithful high-resolution images of protein surfaces.

Authors:  C Möller; M Allen; V Elings; A Engel; D J Müller
Journal:  Biophys J       Date:  1999-08       Impact factor: 4.033

2.  Following single antibody binding to purple membranes in real time.

Authors:  Ferry Kienberger; Harald Mueller; Vassili Pastushenko; Peter Hinterdorfer
Journal:  EMBO Rep       Date:  2004-05-14       Impact factor: 8.807

3.  Conformational change of bacteriorhodopsin quantitatively monitored by microcantilever sensors.

Authors:  Thomas Braun; Natalija Backmann; Manuel Vögtli; Alexander Bietsch; Andreas Engel; Hans-Peter Lang; Christoph Gerber; Martin Hegner
Journal:  Biophys J       Date:  2006-01-27       Impact factor: 4.033

4.  Atomic force microscope imaging contrast based on molecular recognition.

Authors:  M Ludwig; W Dettmann; H E Gaub
Journal:  Biophys J       Date:  1997-01       Impact factor: 4.033

5.  The height of biomolecules measured with the atomic force microscope depends on electrostatic interactions.

Authors:  D J Müller; A Engel
Journal:  Biophys J       Date:  1997-09       Impact factor: 4.033

6.  In vitro single-cell dissection revealing the interior structure of cable bacteria.

Authors:  Zaixing Jiang; Shuai Zhang; Lasse Hyldgaard Klausen; Jie Song; Qiang Li; Zegao Wang; Bjørn Torger Stokke; Yudong Huang; Flemming Besenbacher; Lars Peter Nielsen; Mingdong Dong
Journal:  Proc Natl Acad Sci U S A       Date:  2018-08-06       Impact factor: 11.205

Review 7.  Visualization of internal in situ cell structure by atomic force microscopy.

Authors:  María L Segura-Valdez; Lourdes T Agredano-Moreno; Alma L Zamora-Cura; Reyna Lara-Martínez; Luis F Jiménez-García
Journal:  Histochem Cell Biol       Date:  2018-09-11       Impact factor: 4.304

8.  Atomic force microscope imaging of phospholipid bilayer degradation by phospholipase A2.

Authors:  M Grandbois; H Clausen-Schaumann; H Gaub
Journal:  Biophys J       Date:  1998-05       Impact factor: 4.033

9.  Thy-1 immunolabeled thymocyte microdomains studied with the atomic force microscope and the electron microscope.

Authors:  J Thimonier; C Montixi; J P Chauvin; H T He; J Rocca-Serra; J Barbet
Journal:  Biophys J       Date:  1997-09       Impact factor: 4.033

10.  Differential stiffness and lipid mobility in the leaflets of purple membranes.

Authors:  Kislon Voïtchovsky; Sonia Antoranz Contera; Miya Kamihira; Anthony Watts; J F Ryan
Journal:  Biophys J       Date:  2005-12-30       Impact factor: 4.033

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