Structure-Based drug design
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How can we best use the data base of threedimensional structures to help us more efficiently
design drugs?
X-ray Crystallography- HIV protease inhibitor
NMR Spectroscopy- SAR by NMR
Computational modeling
Ligand binding sites in macromolecules
Combinatorial chemistry - Huge libraries of small
molecules.
Role of X-ray crystallography
* Capable of providing very high resolution structures
which are needed to determine precise atomic level
descriptions of ligand binding sites.
* Things often crystallize better in the presence of ligand
as a result of increased stability (less floppy regions).
* Once crystallization techniques have been worked out
for one complex, they should be fairly similar with
subsequent complexes.
* Well-suited for studying small samples of molecules
that have been screened by a previous method but not
really suited for library screenings.
Role of NMR spectroscopy
* One is not always able to get high enough resolution
needed for drug design.
* Limited to smaller macromolecules, more or less 30
kDa or less.
* It is a method that is capable of determining the
position of some hydrogen bonds.
* It is suited for rapid screening of large number of
molecules as potential ligands using SAR by NMR.
* It can be very quick at mapping residues that are
altered following ligand binding.
Why is it so hard?
* Proteins exist in many different conformational states
which influence and are influenced by ligand binding.
* A single fixed protein structure represents only a very
narrow window for ligand binding.
* We must learn how to accommodate loop fluctuations
and domain movement in our design regimens.
* We must learn how to deal with solvents and
electrostatic interactions if we hope to make more
accurate predictions of binding strengths.
SAR by NMR
* NMR-based screening method.
* Uses a simple (quick) experiment to identify small
organic molecules that bind to proximal subsites of
a protein.
* The molecules are then linked together to produce
high-affinity ligands.
* This can be extremely powerful when used with
small molecule libraries to identify lead-compounds
Shuker et al., Science 274, 1531-1534 (1996).
Outline of SAR by NMR
Shuker et al., Science 274, 1531-1534 (1996).
Outline of SAR by NMR
Shuker et al., Science 274, 1531-1534 (1996).
Outline of SAR by NMR
Shuker et al., Science 274, 1531-1534 (1996).
Outline of SAR by NMR
Shuker et al., Science 274, 1531-1534 (1996).
Outline of SAR by NMR
Shuker et al., Science 274, 1531-1534 (1996).
Outline of SAR by NMR
SAR by NMR applied to Bcl-xL
Bcl (B-Cell Lymphoma) family of proteins plays a key
role in maintenance of normal cellular homeostasis.
Overexpression leads to oncogenic transformations and
plays a role in drug resistance in certain forms of cancer.
The family of protein consists of both antiapoptotic (Bcl-2,
Bcl-xL) and proapoptotic (Bak, Bax, Bad) members.
The structure of several family members is known.
The structure consists of two hydrophobic helices
surrounded by 5 to 7 amphipathic helices.
The antiapoptotic members have a groove that binds to an
-helice (BH3) present in the proapoptotic members.
Petros et al., J Med Chem 49, 656-663 (2006).
Identification of first Bcl-xLsite.
Performed NMR based screen to identify molecules that
would compete with binding of proapoptotic proteins to
Bcl-xL.
Identified that several biaryl compounds bound to the same
binding pocket of Bcl-xL as proapoptotic proteins.
These compounds bind in the same position as a conserved
leucine residue in the BH3 helice
This served as first binding site for SAR by NMR protocol
applied to Bcl-xL.
Petros et al., J Med Chem 49, 656-663 (2006).
Affinities of selected biaryl compounds to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
Biaryl acid bound to Bcl-xL
Black: HSQC of 15N-Bcl-xL.
Red: HSQC of 15N-Bcl-xL with
biaryl acid (Compound 1).
Petros et al., J Med Chem 49, 656-663 (2006).
Identification of first Bcl-xLsite.
Performed additional NMR based screen to identify
molecules that would bound to a different region of Bcl-xL.
Identified that several aromatic compounds that bound to
and adjacent binding pocket of Bcl-xL as proapoptotic
proteins.
These compounds bind in the same position as a conserved
isoleucine residue in the BH3 helice
This served as second binding site for SAR by NMR
protocol applied to Bcl-xL.
Petros et al., J Med Chem 49, 656-663 (2006).
Affinities of selected second site Bcl-xLbinders
Petros et al., J Med Chem 49, 656-663 (2006).
Napthol analog bound to Bcl-xL
Black: HSQC of 15N-Bcl-xL.
Red: HSQC of 15N-Bcl-xL with
biaryl acid (Compound 1).
Green: HSQC of 15N-Bcl-xL with
napthol (Compound 11).
Petros et al., J Med Chem 49, 656-663 (2006).
SAR by NMR applied to Bcl-xL
Compound 11
Compound 1
Petros et al., J Med Chem 49, 656-663 (2006).
SAR by NMR applied to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
SAR by NMR applied to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
SAR by NMR applied to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
Affinities of acylsulfonamides to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
SAR by NMR applied to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
Structure of compound 31 bound to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
SAR by NMR applied to Bcl-xL
Petros et al., J Med Chem 49, 656-663 (2006).
