SUPPORTING INFORMATION
Phototriggerable 2’,7-caged Paclitaxel Radu A. Gropeanu1, Hella Baumann2, Sandra Ritz1, Volker Mailänder1,3, Thomas Surrey2, Aránzazu del Campo1* 1
Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany. Tel
+49 6131 379563; Fax +49 6131 379271, e-mail:
[email protected] 2
Microtubule Cytoskeleton Laboratory, London Research Institute, Lincoln's Inn Fields
Laboratories, 44 Lincoln's Inn Fields, London WC2A 3LY, United Kingdom 3
3rd Department of Medicine (Hematology, Oncology, and Pneumology), University Medical
Center of Johannes Gutenberg-University Mainz, Langenbeckstr. 1, 55131 Mainz, Germany
S1
0.838
1.12
5
10
5
10
4
104
10
3
10
10
2
10
10
0.1% DMSO 3
2
0
20044 0
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29884 0
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48.7
105
10
0
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10
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37.0
105
4
150K
4
100 nM PTX 103
103
102
10
100 nM 2’7-bisNvoc-PTX Pre-irradiated
3tsphiP oneH
A F og)647(l
0
10
5
10
0
30760 0
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2
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32.3
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29475 0
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10
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29045 0
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36.9
29587 0
10
50 µM 2’7-bisNvoc-PTX
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0
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1.13
31571
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250K
1.43
0
29242 0
50K
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250K
Propidium Iodide (lin)
Figure S7. Dot plots of the FACS analysis data of HeLa cells. Data are shown from two independent experiments of HeLa cells after 20 h incubation in medium containing DMSO, PTX and caged derivatives at indicated concentrations respectively. The plots show the antiphospho histone H3 serine 10 labeling intensities (indicative of the mitotic cells) versus the intensity of the propidium iodide nucleic acid stain (indicative of the total amount of DNA per cell). S2
