force-spectroscopy of single proteins ii: mechanical engineering in biological systems

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Force-spectroscopy of single proteins II: mechanical engineering in biological systems

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Page 1: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Force-spectroscopyof single proteins

II: mechanical engineering in biological systems

Page 2: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Igor Demonstration of analysis with models of

polymer elasticity

Page 3: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Reverse Engineering of Reverse Engineering of the the

giant muscle protein titingiant muscle protein titin

Page 4: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 5: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

The elastic protein titin is the third filament of muscle

Page 6: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Electron micrographs of isolated titin molecules

Page 7: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 8: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 9: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Machina Carnis

Page 10: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

A

B

C

D

Titin: a complex mechanical protein

Adapted from Linke, 2007, Cardiovascular Research (in press)

Page 11: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Measuring the extensibilityof titin in a single

isolated cardiac fiber

Page 12: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 13: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
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Page 15: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
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Page 17: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Elasticity of PEVK

Page 18: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Electron micrographs of PEVK_I27 polyprotein

Page 19: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Persistence length of PEVK

Page 20: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Elasticity of N2B

Page 21: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 22: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
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Page 26: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

V13P

V11P V15P

wt Y9P

Page 27: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Understand the mechanical design of titin in humans

Create titin phenotypes in mice

Understand the molecular design of its modules

Page 28: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Mechanical design of Mechanical design of the extracellular matrix:the extracellular matrix:

fibronectinfibronectin

Page 29: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

A complex web of proteins and polysaccharides that provides

the mechanical scaffold for organs and tissues

cell membrane

ECM

Page 30: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

NMR structure of 10F3. The RGD residues are identified in the picture.

Fibronectin: a major, cell binding component of the ECM

Page 31: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 32: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Fluorescently labeled fibronectin assembled by CHO cells

Page 33: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 34: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
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Mechanical unfolding of protein domains helps to keep the cells mechanically bonded.

Mechanical hierarchies define the triggers of cellular activity

Cell binding

cryptic

binding

cryptic

binding

Page 39: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Mechanical design of Mechanical design of the extracellular matrix:the extracellular matrix:

polysaccharidespolysaccharides

Page 40: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

amylose

Polysaccharidescellulose

Page 41: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

If we mechanically stretch a sugar ring, it gets longer by switching from a chair to a boat conformation

0.45 nm0.55 nm

Page 42: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 43: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Periodate oxidation cleaves the rings of pectin

Page 44: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 45: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 46: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Ubiquitin chains form a Ubiquitin chains form a mechanical signallingmechanical signalling

system in cellssystem in cells

Page 47: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 48: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

From Weissman, Nature Reviews, 2001, 2:169-178

Page 49: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
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0=4 x 10-4; x=0.25

Page 53: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 54: Force-spectroscopy of single proteins II: mechanical engineering in biological systems
Page 55: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

1.0

0.8

0.6

0.4

0.2

0.0

Pu

nfo

ld (

fo

r t=

1/0

.05

min

-1 )

12 3 4 5 6 7 8 9

102 3

n

n=4

F = 57 pN

n

nkT

Fdx

etentP

01),(

A)

B)

F

n

proteasome polyubiquitin

Targeted protein

Page 56: Force-spectroscopy of single proteins II: mechanical engineering in biological systems

Conclusions

2.- Titin has a complex mechanical design with multiple mechanical elements that combine to create the finely tuned muscle elasticity.

3.- The extensibility of titin can be calculated from single molecule data and then scaled up to explain elasticity in situ.

1.- Single molecule force spectroscopy combined with protein engineering can examine the mechanical design of complex protein structures

4.- This paradigm can be extended to many other biological systems