traveling through proteomes using 3d-em and afm nanoanalysis, july 10, 2006, ethz andreas engel...

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Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of Basel, Switzerland

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Page 1: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Traveling Through Proteomes Using 3D-EM and AFM

Nanoanalysis, July 10, 2006, ETHZAndreas Engel

Maurice E. Müller Institiute, Biozentrum

University of Basel, Switzerland

Page 2: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Electron Tomography

Page 3: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

MPI of Biochemistry Max Planck Society

3D-object => set of 2D-projections3D-object => set of 2D-projections 2D-projections => 3D-2D-projections => 3D-reconstructionreconstruction

Principle of electron tomographyPrinciple of electron tomography

W. Baumeister, R. Grimm, J. Walz: Trends Cell Biol 9 (1999) 81-85W. Baumeister, R. Grimm, J. Walz: Trends Cell Biol 9 (1999) 81-85

Page 4: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Weighted Backprojection

QuickTime™ and aDivX® 5.0 decompressor

are needed to see this picture.

Page 5: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

MPI of Biochemistry Max Planck Society

Zur Anzeige wird der QuickTime™ Dekompressor „Photo“

benötigt.

Sporozoites (Sporozoites (Plasmodium bergheiPlasmodium berghei))

Page 6: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

MPI of Biochemistry Max Planck Society

membranemembrane

microtubulesmicrotubules

ERER

dense granulesdense granules

rhoptriesrhoptries

micronemesmicronemes

polar ringspolar rings

Apical part of a sporozoite cellApical part of a sporozoite cell

Page 7: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Nanoanalytics of Soluble Complexes:

Scanning Transmission Electron Microscopy (STEM)

Page 8: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Scanning Transmission EM

200 Å

Philippe Ringler

Page 9: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

STEM HardwareBF DF

Acceleration voltage 100 kVPressure: < 10-10 Torr

Beam current

Single electron counting

PM

Page 10: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

TMV Analysis

14 nm

Page 11: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Actin

Collaboration with Ueli Aebi, M.E. Müller Insitute

Page 12: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

STEM

Mueller et al, J Mol Biol 99

From mass to shape

Page 13: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Nanoanalytics of Membrane Complexes:

Atomic Force Microscopy (AFM)

Page 14: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Membrane Proteins exist in the Bilayer

QuickTime™ and a decompressor

are needed to see this picture.

Bert de Groot & Helmut Grubmüller

Page 15: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Example: Bacteriorhodopsin

Page 16: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Cytosolic Surface of Bacteriorhodopsin

Dimitrios Fotiadis, unpublished

Page 17: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

CS of Bacteriorhodopsin: Force-induced Conformational

Changes

Müller et al. (1995), J. Mol. Biol. & Fotiadis et al. (2002), Micron

10 nm (A), 4 nm (B, C and D)

Page 18: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

The Surface Dynamics of Bacteriorhodopsin

Scheuring et al., European Biophysics Journal

Similarity ranked imagesare assembled into a movie

QuickTime™ and aTIFF decompressorare needed to see this picture.

Low force

High force

QuickTime™ and aTIFF decompressorare needed to see this picture.

Page 19: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Bacteriorhodopsin: Surface Energy Landscape

6 kT

pd(r) peak positionprobability ofdomain d

Fd = -kTlnpd(r)

Scheuring et al.Eur Biophys J2002

Low force

High force

Low force High force

Page 20: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Unzipping Bacteriorhodopsin

Oesterhelt et al. Science 2000

Page 21: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

Conclusions

• Electron and atomic force microscopies offer great tools for cellular nanoanalytics

• Electron tomography provides entire picture of a cell

• STEM makes the link between mass and shape

• AFM is an ideal tool for assessing structure & dynamics of membrane proteins

Page 22: Traveling Through Proteomes Using 3D-EM and AFM Nanoanalysis, July 10, 2006, ETHZ Andreas Engel Maurice E. Müller Institiute, Biozentrum University of

AcknowledgmentsAFMDaniel Müller*Simon Scheuring* Dimitrios FotiadisPatrick Frederix

2D crystallizationHervé RémigyThomas KaufmannThomas Walz*

Protein expressionNora EiflerMyriam DuckelyPaul Werten

Peter AgreWolfgang BaumeisterYoshi FujiyoshiHelmut GrubmüllerBert deGrootKris Palczewski

STEMShirley MüllerPhilippe RinglerFrancoise Erne-Brand