Evaluation of Chemical Labeling Strategies for Monitoring HCV RNA using Vibrational Microscopy

Similar documents
Use of degradable cationic surfactants with cleavable linkages for enhancing the. chemiluminescence of acridinium ester labels. Supplementary Material

Self-organization of dipyridylcalix[4]pyrrole into a supramolecular cage for dicarboxylates

Analytical Method for 2, 4, 5-T (Targeted to Agricultural, Animal and Fishery Products)

Electronic Supplementary Information

Supporting Information

Supporting Information for. Boronic Acid Functionalized Aza-Bodipy (azabdpba) based Fluorescence Optodes for the. analysis of Glucose in Whole Blood

Christophe Lincheneau, Bernard Jean-Denis and Thorfinnur Gunnlaugsson* Electronic Supplementary Information

Manganese powder promoted highly efficient and selective synthesis of fullerene mono- and biscycloadducts at room temperature

ph Switchable and Fluorescent Ratiometric Squarylium Indocyanine Dyes as Extremely Alkaline Sensors

Synthesis and Blastocyst Implantation Inhibition Potential of Lupeol Derivatives in Female Mice

mm C3a. 1 mm C3a Time (s) C5a. C3a. Blank. 10 mm Time (s) Time (s)

All chemicals were obtained from Aldrich, Acros, Fisher, or Fluka and were used without

Supporting Information. Efficient copper-catalyzed Michael addition of acrylic derivatives with primary alcohols in the presence of base

Supporting Information

A pillar[2]arene[3]hydroquinone which can self-assemble to a molecular zipper in the solid state

Development of a near-infrared fluorescent probe for monitoring hydrazine in serum and living cells

Organic and biochemical synthesis of monolignol biosynthetic pathway intermediates

Analysis of fatty acid metabolism using Click-Chemistry and HPLC-MS

Supporting Information

Microwave heating in peptide side chain modification via sulfhydryl reaction

Supporting Information for

Supporting Information

Triptycene-Based Small Molecules Modulate (CAG) (CTG) Repeat Junctions

Supporting Information. Radical fluorination powered expedient synthesis of 3 fluorobicyclo[1.1.1]pentan 1 amine

p-toluenesulfonic Acid-Mediated 1,3-Dipolar Cycloaddition of

Supplemental Material

Supporting Information

Novel D-erythro N-Octanoyl Sphingosine Analogs As Chemo- and Endocrine. Resistant Breast Cancer Therapeutics

Thiol-Activated gem-dithiols: A New Class of Controllable. Hydrogen Sulfide (H 2 S) Donors

Synthetic chemistry-led creation of a difluorinated biaryl ether non-nucleoside reverse transcriptase inhibitor

Highly enantioselective tandem enzyme-organocatalyst crossed aldol reactions. with acetaldehyde in deep-eutectic-solvents.

Electronic Supplementary Material

Supporting Information

SUPPLEMENTAL FIGURE 1 Structures and IC50 values of compounds 13 32

Allenylphosphine oxides as simple scaffolds for. phosphinoylindoles and phosphinoylisocoumarins

Supporting Information: Cis-to-Trans Isomerization of Azobenzene Investigated by Using Thin Films of Metal-Organic Frameworks

Supplementary Information

Supporting Information. Nitrodibenzofuran: a One- and Two-Photon Sensitive Protecting Group that is Superior to

Supporting Information. First synthetic entry to the trimer stage of 5,6-dihydroxyindole polymerization: orthoalkynylaniline-based

Supporting Information. for. Access to pyrrolo-pyridines by gold-catalyzed. hydroarylation of pyrroles tethered to terminal alkynes

Electronic Supplementary Information

Electronic Supplementary Information. Quinine/Selectfluor Combination Induced Asymmetric Semipinacol Rearrangement of

Thermal shift binding experiments were carried out using Thermofluor 384 ELS system. Protein

Supporting Information

Supporting Information. for. Synthesis of 2,1-benzisoxazole-3(1H)-ones by basemediated. photochemical N O bond-forming

L-Carnosine-Derived Fmoc-Tripeptides Forming ph- Sensitive and Proteolytically Stable Supramolecular

Supporting Information

Supplementary Notes. HTS compatible FRET-based conformational sensors clarify membrane receptor activation

Nitro-Grela-type complexes containing iodides. robust and selective catalysts for olefin metathesis

Supporting Information

Supplementary Figures

Heparin Sodium ヘパリンナトリウム

Photoinitiated Multistep Charge Separation in Ferrocene-Zinc Porphyrin- Diiron Hydrogenase Model Complex Triads

Imidazolium Ionic Liquids Containing Selenium: Synthesis and Antimicrobial Activity

Supplementary Materials

Supplemental Information. Reactivity of Monovinyl (Meth)Acrylates Containing Cyclic Carbonates

Catalytic decarboxylative alkylation of β-keto acids with sulfonamides via the cleavage of carbon nitrogen and carbon carbon bonds

Preparation, isolation and characterization of N α -Fmoc-peptide isocyanates: Solution synthesis of oligo-α-peptidyl ureas

Enantioselective synthesis of anti- and syn-β-hydroxy-α-phenyl carboxylates via boron-mediated asymmetric aldol reaction

An Orthogonal Array Optimization of Lipid-like Nanoparticles for. mrna Delivery in Vivo

Supplementary Figure 1. Chemical structures of activity-based probes (ABPs) and of click reagents used in this study.

Supporting Information

Fig.S1 ESI-MS spectrum of reaction of ApA and THPTb after 16 h.

Zinc Chloride Promoted Formal Oxidative Coupling of Aromatic Aldehydes and Isocyanides to α- Ketoamides

Supplementary Materials Contents

Organic Semiconducting Nanoparticles as Efficient Photoacoustic Agents for Lightening Early Thrombus and

PHOTOCATALYTIC DECONTAMINATION OF CHLORANTRANILIPROLE RESIDUES IN WATER USING ZnO NANOPARTICLES. DR. A. RAMESH, Ph.D, D.Sc.,

Electronic Supporting Information

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2007

Supplementary Material (ESI) for Chemical Communications This journal is (c) The Royal Society of Chemistry 2008

Dual-site Controlled and Lysosome-targeted ICT-PET-FRET. Fluorescent Probe for Monitoring ph Changes in Living Cells

Naoya Takahashi, Keiya Hirota and Yoshitaka Saga* Supplementary material

An efficient methodology to introduce o-(aminomethyl) phenyl-boronic acids into peptides: alkylation of secondary amines

Supporting Information for. Use of the Curtius Rearrangement of Acryloyl Azides in the Synthesis of. 3,5-Disubstituted Pyridines: Mechanistic Studies

Supporting Information

Global profiling of dynamic protein palmitoylation

Supporting Information

Electronic Supporting Information

Supporting information

Supporting Information. Design and Synthesis of Bicyclic Pyrimidinones as Potent and Orally. Bioavailable HIV-1 Integrase Inhibitors.

Supporting Information. Copper-catalyzed cascade synthesis of benzimidazoquinazoline derivatives under mild condition

Supporting Information

Supporting Information

Supporting Information

Lewis acid-catalyzed regioselective synthesis of chiral α-fluoroalkyl amines via asymmetric addition of silyl dienolates to fluorinated sulfinylimines

Masatoshi Shibuya,Takahisa Sato, Masaki Tomizawa, and Yoshiharu Iwabuchi* Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences,

Cytosolar delivery of large proteins using nanoparticlestabilized

Stereoselective Aza-Darzens Reactions of Tert- Butanesulfinimines: Convenient Access to Chiral Aziridines

Supplementary Information Titles

Issue in Honor of Prof. Edmund Lukevics ARKIVOC 2006 (v) 86-91

Development of a Cell-penetrating Peptide that Exhibits Responsive. Changes in its Secondary Structure in the Cellular Environment

Supplementary Materials

Pt IV azido complexes undergo copper-free click reactions with alkynes

Direct Aerobic Carbonylation of C(sp 2 )-H and C(sp 3 )-H Bonds through Ni/Cu Synergistic Catalysis with DMF as the Carbonyl Source

Detection of Low Level of Chloramphenicol in Milk and Honey with MIP SPE and LC-MS-MS

August Determination of Pindone in Agricultural Products by LC-MS/MS

Supporting Information. for. Synthesis of dye/fluorescent functionalized. dendrons based on cyclotriphosphazene

Supporting Information

Methyltrioxorhenium-Catalyzed Highly Selective Dihydroxylation of 1,2-Allenylic Diphenyl Phosphine Oxides

Design, synthesis and evaluation of ph-dependent hydrolysable emetine analogs as treatment for prostate cancer.

Transcription:

Electronic Supplementary Information Evaluation of Chemical Labeling Strategies for Monitoring HCV RA using Vibrational Microscopy Matthew oestheden 1,2, Qingyan Hu 1, Angela M. Tonary 1, Li-Lin Tay 3, John Paul Pezacki 1,2, 1 The Steacie Institute for Molecular Sciences, The ational Research Council of Canada, ttawa, Canada, 2 Chemistry Department, University of ttawa, ttawa, Canada 3 The Institute for Microstructural Sciences, The ational Research Council of Canada, ttawa, Canada Table of contents 1. HPLC/LC-MS Analysis of ormal and Modified HCV RA S2 2. Synthesis of 4-C-M S2 3. C Modification of aau-hcv RA S3 4. Figures S1 S9 S4 S12 Correspondence: John.Pezacki@nrc.ca S1

1. HPLC/LC-MS Analysis of ormal and Modified HCV RA In order to separate and quantify the relative proportions of modified and unmodified RA bases, HPLC conditions were first optimized to distinguish the individual monomeric nucleotides (Figure S8). After several trials we determined that the following conditions were optimal:.1 M H 4 Ac, ph 6.5 at a flow-rate of.2 ml/min. Before the optimized HPLC/LC-MS conditions were applied to the analysis of modified RAs, digestion and dephosphorylation of HCV RA and aau-hcv RA were performed to obtain the constituent mononucleosides. HPLC/LC-MS analysis clearly showed that the mononucleoside components of HCV RA and aau-hcv RA were resolved following digestion and dephosphorylation as described in the materials and methods (Figure S2). To determine if the digestion conditions were achieving maximal sample decomposition, the concentration and time dependence of the reaction was examined. The results of the concentration dependence experiment showed that the HCV RA and aau-hcv RA reactions appeared to saturate with 1 25U of S1 nuclease (Figure S9A). Furthermore, the time dependence experiment showed that the digestion reaction saturated after 1 hour (Figure S9B). 2. Synthesis of 4-C-M C Cl H 2 CH 2 Cl 2, rt HBC C 1) CF 3 CH, rt 2) /Et3, CH 2 Cl 2 HBC H 3) Ac 2, Aca, 1 C, 1 hr H C 1 4-C-M 4-Cyano-benzoyl chloride (3 mg, 1.8 mmol) was suspended in 6 ml dichloromethane. -BC-1,2-ethylenediamine (32 µl, 2. mmol) and 3 µl triethylamine in 6 ml dichloromethane was added under argon. The mixture was stirred for 3 min and then rotavaped to dry. The residue was triturated in 5 ml ethyl acetate. The precipitate was collected by vacuum filtration to give crude 1, -BC-1,2-(4- cyanobenzamido)ethylenediamine (432 mg, 83%). Crude 1 (289 mg, 1. mmol) was dissolved in.8 ml trifluoroacetic acid and stirred overnight. The volatile components were removed under vacuum. The residue was added 2 µl triethylamine and dissolved in 2 ml dichloromethane under argon. Maleic anhydride (18 mg, 1.1 mmol) was added and the mixture was stirred for 45 min under argon and then rotavaped to dry. The residue was triturated in 2 ml water. The precipitate was collected by vacuum filtration and washed with 2 ml of ethyl acetate to give 135 mg of white solid (47%). This white solid was added.8 ml acetic anhydride and 45 mg of anhydrous sodium acetate. The mixture was heated at 1 C for 1 hr After cooling down, 15 ml ice water was added and the mixture was stirred for another hour. Then it was brought to basic by added sodium carbonate. The precipitate was collected by vacuum filtration and purified by silica column chromatography (8:2 of ethyl acetate: hexane) to give final product 3. 1 H MR (4 MHz) 7.97 (d, 2H), 7.89 9d, 2H), 6.87 (s, 2H), 3.74 (t, 3H), 3.64 (t, 2H). FAB-MS (M+1) calculated 27.1; found 27.1. S2

3. C Modification of aau-hcv RA To overcome stereoelectronic effects in the cyano-labeling of HCV RA we utilized 3-cyanobenzyl-HS to label aau-163mer. Again, initial analysis of the electrophoretic migration showed an increase in the apparent mass of labelled aau- 163mer, which was consistent with a successful reaction (Figure S4A). HPLC comparison to control reactions clearly showed the appearance of a new product at 23.6 min., with a corresponding disappearance of the aau peak at 1.5 min., both of which were indicative of a successful reaction (Figure S4C). ESI-MS analysis of the digested nucleoside mixture showed a signal for the 3-C-modified aau (aau-c; m/z = 429). Electrophoretic analysis of C-HCV RA revealed a mass-shift that was consistent with those seen for Bz-HS and 3-C-HS modified aau-163mer (Figure S5A). Furthermore, the presence of the peak believed to be aau-c was immediately apparent at 23.6 min (Figure S5B). We conclude that 3-C-HS successfully modified aau-hcv RA. S3

A) 4 nt 2 nt L 1:1 1:2 1:4 B) 18 16 14 12 1 8 6 4 2 C U aau G A 1:1 1:2 1:4 Figure S1. Regulating the extent of aau incorporation. A) Electrophoretic migration of HCV RA compared to aau-hcv RA synthesized with decreasing amounts of aau. As the amount of aau is decreased the migration of aau-hcv RA begins to approach that of HCV RA. B) HPLC analysis displayed a reciprocal relationship between aau and U as the concentration of aau in the transcription reaction was decreased. X:Y = aau:utp in transcription reaction. S4

G 13. min. A 21.1 min. C 3.9 min. U 5.9 min. 2 5 8 11 14 17 2 aau 11. min. 2 5 8 11 14 17 2 Figure S2. HPLC resolution of digested and dephosphorylated RA. HCV RA (top) clearly showed the presence of C, U, G and A. Analysis of aau-hcv RA (bottom) showed an additional eluent that corresponded to aau. Samples were detected at 254 nm. S5

A) 25 2 ii iii mau 15 1 5 i 3 5 7 9 11 13 15 17 19 21 23 25 aau + Bz Bz-HS aau B) i ii iii H 2 H H H R R m/z = 317 m/z = 421 m/z = 237 Figure S3. Evaluating aau modification with Bz-HS. A) Bz-HS eluted at 22.5 min. (blue). In the presence of aau a new peak at 23.6 min. (pink) appeared, in addition to the Bz-HS peak. This coincided with the disappearance of the aau peak at 1.6 min. (green). B) Structures of aau (i), aau-bz (ii) and Bz-HS (iii). LC-MS confirmed the identity of the peaks corresponding to these materials. R = dephosphorylated ribose sugar. S6

A) 5 nt 2 nt L C Bz 5 nt 2 nt L C C B) A C U aau G 3 7 1 13 17 2 23 Bz Ctrl C) H H C m/z = 429 R aau-c 23.6 min. 3 7 1 13 17 2 23 3C Ctrl Figure S4. Labeling of a model RA system with Bz-HS and 3-C-HS. A) Electrophoretic migration of 163mer modified with Bz-HS (left) and 3-C-HS (right). Labeled products showed an increase in apparent mass. B) HPLC showing the disappearance of aau (1.6 min.) and the appearance of Bz-modified aau (23.6 min.) when control (Ctrl, blue) and Bz-modified (Bz, pink) 163mer reactions were analyzed. C) HPLC comparison of 163mer control (Ctrl, blue) and 3-C-HS (3C, red) labeling reactions showing the appearance of aau-c (23.6 min.) and corresponding disappearance of aau (1.6 min.). S7

A) L aau C ~ 1, nt 4 nt 2 nt B) G C H R H m/z = 429 C A U aau-c 2 7 12 17 22 Figure S5. Analysis of C-HCV RA. A) Electrophoretic analysis showed a mass-shift upon modification of aau-hcv RA that indicated a successful reaction. B) The clear disappearance of aau (1.6 min.) and appearance of aau-c (23.6 min.) was also indicative of a successful labeling reaction. L = RA Ladder; = HCV RA; aau = aau-hcv RA; C = C-HCV RA. S8

Diameter (nm) Spread (nm) HCV RA 3.7 17.7 aau-hcv RA 28.5 14.7 D-HCV RA 24.3 1. C-HCV RA 31.6 17.5 Figure S6. DLS analysis of modified HCV RAs. o clear difference between the normal and modified HCV RAs could be resolved using DLS. However, the size of the collapsed state approximated that required to fit inside the mature HCV virion (~3 nm). All values are reported as mean of 1 measurements. Diameter = mean hydrodynamic diameter; Spread = size of population distribution. S9

1 9 RLU/(mg/mL) 8 7 6 5 4 3 Cells Mock D-RA D-rATP D-rUTP D-rGTP D-rCTP Figure S7. Decreases in luciferase activity were causally linked to the incorporation of specific D-rTPs into HCV replicon RA. Incorporation of deuterated ATP and UTP affected luciferase activity less than deuterated GTP and CTP. The reasons for this remain unclear. All measurements were made in triplicate and are reported as mean values ± one standard deviation. D-RA = D-HCV RA S1

A) C 4.5 min. U 6.4 min. G 12.6 min. aau 1.1 min. A 19.4 min. 4. 6. 8. 1. 12. 14. 16. 18. B) 244. 245. 262.2 179. 237. 315.1 278.9 34.3 423. 475.8 489. 56.4 339.9 556. 559. 584. 15 175 2 225 25 275 3 325 35 375 4 425 45 475 5 525 55 575 6 625 65 675 7 725 75 775 8 487. 177. 237. 246. 181. 279.2 285.2 338.1 341.9 15 175 2 225 25 275 3 325 35 375 4 425 45 475 5 525 55 575 6 625 65 675 7 725 75 775 8 317.1 461. 452.5 353. 391.8 462.9 512. 515.8 568.9 613.262. 623.3 674.8 693.8 15 175 2 225 25 275 3 325 35 375 4 425 45 475 5 525 55 575 6 625 65 675 7 725 75 775 8 3. 4. 5. 6. 7. 8. 9. 1. 11. 12. 13. 14. 15. 16. 17. 18. 19. Figure S8. ptimizing the elution conditions of 5 mononucleosides. A) C, U, A, G and aau were all resolved as shown by this overlay of their respective elution profiles. Samples were detected at 254 nm. B) C, U, A and G were identified by LC-MS as molecular ions (M+1) at a concentration of 1 mm. The modified uridine, aau, was identified from a weekly ionizing ammonium adduct (M+18) at a concentration of 6 mm. Even after accounting for concentration differences the ionization of aau was low. S11

A) 15 1 mau 5 C U G A 5U 25U 1U 2U 2 15 mau 1 5 C U aau G A 25U 5U 1U 2U B) 6 1 5 8 4 mau 3 2 1 C U G A 24 Hr. 8 Hr. 4 Hr. 2 Hr. 1 Hr. mau 6 4 2 C U aau G A 24 Hr. 8 Hr. 4 Hr. 2 Hr. 1 Hr. Figure S9. Validating the digestion of HCV RA and aau-hcv RA. A) The digestion reaction saturated between 2 1U for HCV RA (left) and 1 25U for aau-hcv RA (right). B) The digestion of HCV RA (left) and aau-hcv RA (right) saturated after 2 hours. C and U 2U (A) and 1 Hr. (B) data points were not collected. S12