Transcript
Page 1: Macromolecular Nanomachines In Action

IN ACTION

José Ramón Macías

macromolecularnanomachines

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José Ramón Macías

Hi, my name is:

Bioinformatician

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macromolecularnanomachines

IN ACTION

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Structure

Sequence

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Structure

Function

Sequence

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10 nm

1 mm

100 nm

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X-Ray DiffractionCrystallography

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conformational changes

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Simian Virus 40

Large T antigen

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Simian virus 40(SV40)

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Large T antigen

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Short & straight

Long & straight

Middle curvature

High curvature

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Short & straight

Long & straight

Middle curvature

High curvature

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Bacteriophage SPP1 replicative

Helicase G40P

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D. melanogaster

26S proteasome

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26S proteasome

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X-Ray Crystallography

Requires Crystals

High Resolution

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X-Ray Crystallography

Requires Crystals

High Resolution

3D Electron Microscopy

Medium Resolution

Crystals Not required

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X-Ray Crystallography

Requires Crystals

High Resolution

3D Electron Microscopy

Medium Resolution

Crystals Not required

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X-Ray Crystallography

Requires Crystals

High Resolution

3D Electron Microscopy

Medium Resolution

Crystals Not required

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X-Ray Crystallography

Requires Crystals

High Resolution

3D Electron Microscopy

Medium Resolution

Crystals Not required

Hybrid Models

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X-Ray Crystallography

Requires Crystals

High Resolution

3D Electron Microscopy

Medium Resolution

Crystals Not required

Hybrid Models

Fitting

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3D-EM model Atomic model

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Hybrid model

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GroEL chaperonin

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Anti-tumoralP53 transcription factor

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lectron

icroscopy

ata

ank

E

M

D

B

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10

40

67

117

193

266

363

2002 2003 2004 2005 2006 2007 2008

since June 2002, the number of structures has increasedsteadily.

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Single Particle Icosahedral

HelicalIndividual Structure 2D Crystal

Today there are629 entries

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1 out of 3 structures

are covered by more than one entry

369

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http://biocomp.cnb.csic.es/das/PeppeR

DASx3DEM & PeppeR

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Structure

Sequence

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adopting different conformations

is what leads to function


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