Identification of hPin1 inhibitors that induce apoptosis in a mammalian Ras transformed cell line
Elena Bayer, Michael Thutewohl, Claudia Christner, Thomas Tradler, Frank Osterkamp,
Herbert Waldmann* and Peter Bayer*
Department of Chemical Biology, Max-Planck-Institut für molekulare Physiologie, Otto-Hahn-Str. 11, D44227 Dortmund, Germany, and Universität Dortmund, Fachbereich 3, Organische Chemie, D-44221
Dortmund, Germany Molecular and Structural Biophysics, Max- Planck-Institute for Molecular Physiology,
Otto-Hahn-Str. 11, 44227 Dortmund & Interdisciplinary Centre for Magnetic Resonance, Dortmund, German.
Jerini AG, Invalidenstraße 130, 10115 Berlin, Germany
Methods
Protease coupled Pin1 assay: Measurements were done on a Dynex UV-Vis Reader at 390 nm and 4°C in 35 mM HEPES buffer
(pH 7.8).[6,10] (Ref. 10: G. Fischer, H. Bang and C. Mech, Biomed. Biochim. Acta, 1984, 43, 1101-1111). Ac-Ala-Ala-pSer-ProArg-pNA (120uM) was used as a substrate. The synthesized compounds and hPin1 (6nM) were incubated for 30 min and
measurements started by addition of trypsin (0.19 mg/ml). Under the condition [S0] << Km, recorded progression curves can be
described by first-order kinetics. From the observed rate constant kobs a first-order rate constant kenz for enzymatic catalysis of cis
to trans isomerization can be calculated as kobs=k0+kenz, where k0 represents the first-order rate constant for the non-catalyzed
cis/trans isomerization. Inhibitor constants (IC50) were determined by analyzing the concentration dependence of each inhibitor
on PPIase activity. hPin1 IC50 values of the most active compounds were confirmed by single cell measurements with a Hewlett
Packard 8452A diode array UV/VIS spectrophotometer at 10°C. Specificity against PPIases hCyp18 and hFKBP12 was measured
according to Hennig et al.,1998 using Suc-AFPF-pNA (100 µM) as a peptide substrate and a-chymotrypsin (0.47 mg/ml) as
isomer-specific protease.
NMR measurements: All experiments were performed at a temperature of 300 K on a Varian Inova-600 spectrometer (Varian,
Darmstadt) equipped with shielded Z-gradients. 1D experiments were recorded with unlabeled protein and
15N-HSQC
spectra
(100uM protein, pH 6.8, 50mM phosphate buffer, 50mM sodium sulfate, 10mM 1,4-dithiothreitol) were acquired on uniformly
15N-labeled
samples. 1D precipitation experiments were started by adding a 6 molar excess of the corresponding inhibitor
dissolved in a 100mM DMSO stock solution.
Mass Spectrometry: Mass spectra were recorded on a quadrupole time-of-flight mass spectrometer type Q-TOF micro
(Micromass, Manchester, UK) equipped with a nanoESI source. The capillary voltage was 1200 V, the sample cone voltage 28.0
V and the extraction cone voltage 1.0 V. The source temperature was set to 80 °C, no cone gas flow was used. The mass
spectrometer was calibrated over the mass range m/z 100 to 2000 using a 10 mM solution of phosphoric acid in 30 % 2-propanol.
Spray capillaries were manufactured in-house using a micropipette puller type PB-7 (Narishige, Tokyo, Japan) and coated with
platinum in a sputter coater type SCD 050 (BAL-Tec, Balzers, Liechtenstein). For determination of the accurate molecular mass
of the intact protein, the solution was desalted using C4-ZipTips (Millipore, Bedford, MA, USA). Equilibration of the C 4-ZipTips
and washing of the bound protein was done with 5% formic acid. The protein was eluted with 1-2 µL of 50% acetonitrile/0.1%
formic acid.
S1
S2
Figure 3: A, NMR tubes showing precipitation of a 100M hPin1 solution. Left, control (addition of 3l of a 100mM DMSO
solution), middle, 6-fold molar excess of compound 1, right, 6-fold molar excess of juglone. B, SDS gel under reducing
conditions. S, supernatant, MW, molecular weight marker, P, precipitate.
Figure 4: TOF MS ES+ spectra of juglone-treated and untreated wild type Pin1. A, wild type Pin1 (exp. molecular mass 18108
Da). B, wild type Pin1 treated with a 5-fold molar excess of juglone. Recorded mass spectra revealed new signals representing
molecular masses of Pin1 modified by 2,3,4,5,6 (exp. 18452.5, 18625.0, 18813.5, 18985.6, 19175.5 Da, respectively) and more
juglone (J) molecules. To avoid detection of noncovalent Pin1/juglone adducts, any loosely bound juglone was removed by C4
chromatography of the protein prior to analysis.
Tables 1-3: Compounds investigated as possible Pin1 inhibitors. Inhibitors, leading to apoptosis of a Ras-transformed MDCK-f3
cell line, are labelled with bold letters, inhibitors of Pin1 presented in figure 1 are additionally underlined. Numbers in brackets
refer to the original published compound numbers9b.
Table 1:
HO
1
R
Me
N
HN
O
O
MeO
S3
O
N
Me
Y
O
R2
R1
Entry
R2
O
O
1
NH
N
H
S
O
2
O
N
3
(21)
-OH
4
(20/2)
5
(20/3)
6
(20/4)
-OH
-OH
-OH
O
7
-OH
O
8
-OH
OMe
O
9
O
OH
O
10
O
Table 2:
OH
R2
1
R
3
R
*
HN
O
N
OH
N
H
O
O
O
4
R
entry
R1
R2
S4
*
R3
R4
1
O
D
Me
H
D
D
L
L
L
L
D
D
H
H
H
H
H
Me
Me
H
H
OH
OH
H
H
H
H
H
D
H
H
D
H
H
L
L
D
D
H
Me
Me
H
H
H
H
H
D
H
H
D
H
H
D
H
H
D
Me
H
D
H
H
HOPh=i
2
3
4
5
6
7
8
HOPhHOPhHOPhPhImid
Imid
Imid
i
i
i
i
i
i
i
O
9
Imid
O2N
10
Imid
11
=
ii
ii
ii
ii
12
13
14
15
Imid
Imid
Imid
Imid
Imid
16
Imid
17
Imid
18
Imid
19
Imid
20
ortho
Imid
BnO
21
22
=o
ortho o
meta o
Imid
Imid
L
L
H
H
H
H
23
para o
Imid
D
H
H
N
HN
Imid
HO
HOPh-
S5
Ph-
Table 3:
R2
R1
HN
R4
R3
*
O
N
OH
N
O
O
3
R
O
HO
entry
R1
R2
1
*
R3
R4
D
H
Ph
D
H
Naph
HOPh-
2
(45)
HOPh-
S6