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U SING SIGHT TO EXPLOIT MOLECULAR KNOWLEDGE

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U SING SIGHT TO EXPLOIT MOLECULAR KNOWLEDGE

Andrea Bernini

Strutural Biology Lab – www.sbl.unisi.it andrea.bernini@unisi.it

10/03/2016@Dipartimento Ingegneria dell’Informazione e Scienze Matematiche

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Structural biology is a branch of molecular biology, biochemistry,

and biophysics concerned with the molecular three-dimensional structure of biological macromolecules such as proteins, RNA, and DNA.

Structural bioinformatics is the branch of bioinformatics which is related to the analysis and prediction of the structure of biological

macromolecules. It deals with generalizations about macromolecular 3D structure such as comparisons of overall folds and local motifs, principles of molecular folding, evolution, and binding interactions, and

structure/function relationships, working both from experimentally solved structures and from computational models. Structural bioinformatics can be seen as a part of computational structural biology.

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B IRTH OF S TRUCTURAL B IOLOGY

1958: John Kendrew and 3D structure of myoglobin.

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Oggi: la stessa molecola di mioglobina visualizzata in grafica 3D con un software gratuito

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S TRUCTURAL LEVELS OF PROTEINS

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P ROTEIN FOLDING AND ENERGY

LANDSCAPE

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S IR K ENDREW AND M YOGLOBIN , 1958

This plasticine model of myoglobin, made by Sir John Kendrew, was the first ever model to be made of a protein molecule. In 1958 John

Kendrew (1917-1977) and Max Perutz (1914-2002) were able to produce a model of its 3-dimensional structure, for which they were awarded the Nobel Prize for chemistry in 1962.

The contorted cylindrical shape, showing the track of polypeptide chain, is supported by wooden rods protruding from a pegboard base;

dimensions of base 18" x 1 1/2"; overall height 8 1/2". The forest of rods

obscured the view of the model and made it hard to adjust. Its size made it cumbersome and problematic to move.

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1965: Kendrew commissiona ad A. A. Barker i primi modelli della mioglobina in palline di metacrilato (e li vende a 600$, stimabili in 4’300$ alla data odierna) .

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F ROM PHYSICAL MODELS TO ABSTRACTION ….

The domain I of CD11a (membrane integrin), wire model decorated with pipecleaner (late 90’s)

The same protein rendered by computer graphics (MolMol)

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E ARLIEST C OMPUTER R EPRESENTATIONS

As early as 1964, Cyrus Levinthal and his colleagues at MIT had developed a system that displayed, on an

oscilloscope, rotating "wireframe"

representations of macromolecular structures.

In a similar way, ATARI created the videogame Asteroids in 1979.

Videogame came later than molecular representation but development rate had been different…

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E VANS & S UTHERLAND C OMPUTERS : 1980-1990

During the 1980's, the most popular computer system for crystallographers was manufactured by Evans &

Sutherland. These computers, costing about $250,000 in 1985, displayed the electron density map, and enabled an amino acid sequence to be fitted

manually into the map.

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M OLECULAR GRAPHICS FOR THE MASSES : R OGER S AYLE ' S R AS M OL , 1993

In 1990, Roger entered graduate school in computer science at the University of Edinburgh. Roger developed his program into a more molecular visualization system, and by 1993, it was being used in

teaching and for images in research publications. Roger generously

made the program available to the world scientific community free of charge when he received his Ph.D.

in June, 1993. In January, 1994, Roger was employed by

GlaxoWellcome, which supported the continued development of

RasMol freeware, including the first version for the Macintosh, for the next two years.

www.openrasmol.org

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JMOL, THE MOLECULAR VIEWER OF THE INTERNET AGE

Jmol is a free, open source molecule

viewer in the form of a Java applet. It is

cross-platform,

running on Windows, Mac OS X, and

Linux/Unix systems.

jmol.sourceforge.net

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S OURCES OF MOLECULAR STRUCTURES

Protein Data Bank (www.rcsb.org) – macromolecules e.g. 2O7N

PubChem (pubchem.ncbi.nlm.nih.gov) – small molecules

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B INDING SITE DISCOVERY AND

VIRTUAL DRUG REPOSITIONING FOR PHARMACEUTICAL CHAPERONES

TARGETING HOMOGENTISATE 1,2-

DIOXYGENASE FOR THE TREATMENT OF

THE INBORN ERROR OF METABOLISM

DISORDER A LKAPTONURIA .

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ruptures of muscles, tendons, ligaments

black spots in eyes

blue-black ears black urine

black cartilage

FOTO: Liverpool

+ aortic valve disease

deficiency of homogentisate 1,2-dioxygenase (HGD) and incapacity to metabolise homogentisic acid (HGA)

(LaDu et al. 1958) -inborn error of metabolism

 HGA accumulates in the body at 2,000 times the normal rate, in form ochronotic pigment it is attacking the bones and turning them black and brittle

 it causes severely debilitating osteoarthritis, heart disease, and other serious health complications

 patients become increasingly disabled as they get older

 the first genetic disease to be discovered more than 110 years ago (MIM 203500; Garrod 1908)

ALKAPTONURIA (AKU)

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ALKAPTONURIA (AKU)

- world-wide incidence is 1:250 000 – 1: 1 000 000

http://www.indiegogo.com/projects/cure-black-bone-disease

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• mapping of the AKU gene to 3q13.33 (Pollak et al. Nat Genet 1993, Janocha et al. Genomics 1994)

• the HGD gene and cDNA described (Granadino et al. Genomics 1997, Fernandez-Canon et al. Nat Genet 1996)

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HGD protein -> dimer of trimers

 expressed mainly in liver, kidneys and prostate (Fernandez-Canon et al. Nat Genet 1996)

 crystal structure described (Titus et al. Nat Struct Biol 2000)

 expression also in chondrocytes, synoviocytes, osteoblasts (Lischi et al. J Cell Physiol 2012)

Rodriguez et al. Hum Mol Genet 2000

HGD trimer side view of hexamer – dimer of

trimers

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AKU – autosomal recessive inheritance father mother

healthy healthy

AKU healthy healthy healthy

child

healthy AKU healthy carrier healthy healthy

carrier carrier

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Binding site discovery workflow

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HGD pockets

HGD structure

with pockets

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HGD pockets

View of HGD pockets in

surface

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Representation of a pocket

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Virtual screening

 A set of molecules are tested in each pocket by molecular docking

simulation

 The affinity between pockets and molecules are calculated

 The molecules with higher affinities are potential chaperones stabilizing the protein- protein interface

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A KNOWLEDGMENTS

Ottavia Spiga

Silvia Galderisi

Neri Niccolai Alfonso Trezza

Vittoria Cicaloni

Annalisa Santucci

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