the structural basis of the cross-bridge cycle

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The structural basis of the cross-bridge cycle

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The structural basis of the cross-bridge cycle. DECORATED ACTIN was the first em reconstruction Moore, Huxley, and DeRosier 1970 J. Mol Biol. Reconstruction by filtered least squares. Projection every 1° (181 projections) Number of observational equations is 161 x 181=29141 - PowerPoint PPT Presentation

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Page 1: The structural basis of the cross-bridge cycle

The structural basis of the cross-bridge cycle

Page 2: The structural basis of the cross-bridge cycle

DECORATED ACTIN

was the first em reconstruction

Moore, Huxley, and DeRosier

1970 J. Mol Biol.

Page 3: The structural basis of the cross-bridge cycle

Reconstruction by filtered least squares

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P f = g

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The classical solution to the equations

P f= g + e

which minimises the sum of squares oferror seTe is

PT P f = PTg

PT P is th enorma l o r Hessia n matrix

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The solution is

f = (PTP)-1 PTg

but PTg is the back projection.

Thus the inverse least squares matrix (PTP)-1

provides the analytical filter for turning theback projection into the required density

Page 8: The structural basis of the cross-bridge cycle

Projection every 1° (181 projections)

Number of observational equations is

161 x 181=29141

Order of normal matrix 17645.

Problem should be well determined

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Oops!!

Page 10: The structural basis of the cross-bridge cycle

Crowther, R. A., DeRosier, D. J. and Klug, A. (1972) The reconstruction of a three-dimensional structure from projections and its application to electron microscopy. Proc. Royal Soc. London 317A: 319-40.

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Case 2. Projection every 3°, not enough data to invert the normal matrix. How much data is there?

To determine the rank of a positive (semi) definite matrix we determine its eigenvalue spectrum

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Decorated actin at 13Å resolving power calculated by filtered least squares

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Electron cryo-microscopy (of decorated actin) shows how strong binding of myosin to actin releases nucleotide Holmes, Angert, Kull, Jahn, Schroeder (2003) Nature 425, 423-427

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Four sub-domain refinement

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The cross-bridge cycle

As revealed by crystallography

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Geeves, M.A. & Holmes, K.C. (2005)

The molecular mechanism of muscle contraction

Adv Protein Chem 71, 161-93

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Lymn & Taylor, 1971

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The myosin motor domain must move the lever arm from pre- to

post- power stroke.

It must bind to actin strongly or weakly

Both functions are controlled by ATP binding and hydrolysis

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Crystallography on the motordomain (particularly Dictyostelium Myosin 2) shows two conformations of myosin:

lever UP and lever DOWN

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Diskussionsthemen• Nennen Sie die Hauptthesen,

über die Sie sprechen werden.

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Thema 1• Details über das Thema

• Argumente und Beispiele

• Warum ist das Thema für Ihr Publikum von Bedeutung?

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switch 1

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QuickTime™ and aApple Motion JPEG Format A decompressor

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Fischer et al (2005) PNAS102 6873-8

QuickTime™ and aSorenson Video 3 decompressorare needed to see this picture.

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Fischer et al (2005) PNAS102 6873-8

QuickTime™ and aSorenson Video 3 decompressorare needed to see this picture.

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Weak and Strong Binding

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Coureux, P. D.Wells, A. L.Menetrey, J.Yengo, C. M.Morris, C. A.Sweeney, H. L.Houdusse, A. (2003)

A structural state of the myosin V motor without bound nucleotide

Nature 425 419-23

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Rayment_chicken

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Upper/lower 50K fitted

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Myo 5

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