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

Similar documents
Supplementary Information

Copyright WILEY-VCH Verlag GmbH, D Weinheim, Supporting Information for Angew. Chem. Int. Ed. Z 18050

One-pot synthesis of dual functional peptides by Sortase A-mediated on-resin cleavage and ligation

Supporting Information

Supporting Information for. PNA FRET Pair Miniprobes for Quantitative. Fluorescent in Situ Hybridization to Telomeric DNA in Cells and Tissue

Novel Water-Soluble Near-Infrared Cyanine Dyes: Synthesis, Spectral Properties, and Use in the Preparation of Internally Quenched Fluorescent Probes

Supporting Information. A fluorogenic assay for screening Sirt6 modulators

Supplementary Material Novel phosphopeptides as surface-active agents in iron nanoparticle synthesis

Dual Use of a Chemical Auxiliary: Molecularly Imprinted Polymers for the Selective Recovery of Products from Biocatalytic Reaction Mixtures

Development and Evaluation of an Albumin-Binding NODAGA-Folate

(A) Effect of I-EPI-002, EPI-002 or enzalutamide on dexamethasone (DEX, 10 nm)

Supporting Information. Fast, Copper-Free Click Chemistry, A Convenient Solid-Phase Approach to Oligonucleotide Conjugation

Supporting Information For:

Postsynthetic modification of unprotected peptides via S-tritylation reaction

Supporting Information

Supporting Information

Convenient Synthesis of Nucleoside 5 -Triphosphates for RNA Transcription. Supplemental Materials

Supporting Information

Supporting Information

Supporting Information

1-N-(3,4,6-tri-O-acetyl-2-deoxy-2-N-acetyl-β-D-glucopyranosylamide)-4-(N -methylidenyl -2 - bromoacetamido)-4,5-anhydro-triazole (5) AcO AcO

Electronic Supplementary Information for

Molecular Imaging of Labile Iron(II) Pools in Living Cells with a Turn-on Fluorescent Probe

Supporting Information

available 3,5-dihydroxybenzoic acid was reduced to afford 3,5-diketohexahydrobenzoic acid in

Supplementary Material A Highly Convenient Procedure for Oligodeoxynucleotide Purification

Supporting Information

Supporting Information

Supporting information. An improved photo-induced fluorogenic alkene-tetrazole reaction for protein labeling

Reduction-free synthesis of stable acetylide cobalamins. Table of Contents. General information. Preparation of compound 1

Supporting Information. Visualization of Phagosomal Hydrogen Peroxide Production by A Novel Fluorescent Probe That Is Localized via SNAP-tag Labeling

Coupling of 6 with 8a to give 4,6-Di-O-acetyl-2-amino-2-N,3-O-carbonyl-2-deoxy-α-Dglucopyranosyl-(1 3)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose.

Backbone modification of a parathyroid hormone receptor-1 antagonist/inverse agonist

General methods. RP-HPLC and LC-MS

Synthesis of Peptide-Grafted Comb Polypeptides via Polymerisation of NCA-Peptides

A selenium-contained aggregation-induced turn-on fluorescent probe for hydrogen peroxide

Post-Synthetic Approach for the Synthesis of 2 -O-Methyldithiomethyl-Modified Oligonucleotides Responsive to Reducing Environment

1G (bottom) with the phase-transition temperatures in C and associated enthalpy changes (in

SUPPORTING INFORMATION

Electronic Supplementary Information. Zhen Zheng, Gongyu Li, Chengfan Wu, Miaomiao Zhang, Yue Zhao, and Gaolin Liang*

Rational design of a ratiometric fluorescent probe with a large emission shift for the facile detection of Hg 2+

Supporting Information. Labeled Ligand Displacement: Extending NMR-based Screening of Protein Targets

Supporting Information

in reaction buffer (40 mm Tris-HCl, ph 8.0, 100 mm NaCl and 10 mm MgCl 2 ). After

SUPPLEMENTARY INFORMATION

2017 Reaction of cinnamic acid chloride with ammonia to cinnamic acid amide

Determination of Carbonyl Compounds In Water by Dinitrophenylhydrazine Derivatization and HPLC/UV*

Rational design of a hexapeptide hydrogelator for controlled-release drug delivery

Supporting Information for DOI: /s Georg Thieme Verlag KG Stuttgart New York Thieme

Super-Resolution Monitoring of Mitochondrial Dynamics upon. Time-Gated Photo-Triggered Release of Nitric Oxide

Amphiphilic diselenide-containing supramolecular polymers

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2008

Supporting Information

Supporting Information

Supplementary Material for: Unexpected Decarbonylation during an Acid- Mediated Cyclization to Access the Carbocyclic Core of Zoanthenol.

Imine Hydrogels with Tunable Degradability for

Rapid Microwave-Assisted CNBr Cleavage of Bead-Bound Peptides

Supporting Information

UPLC for Synthetic Peptides: A User`s Perspective

Supporting Information

(Supplementary Information)

Electronic supplementary information. Strong CIE activity, multi-stimuli-responsive fluorescence and data

Supplementary Materials. Synthesis of Reusable Silica Nanosphere-Supported Pt(IV) Complex for. Formation of Disulfide Bonds in Peptides

Supporting Information. for. Angew. Chem. Int. Ed. Z Wiley-VCH 2003

Solid-phase-supported synthesis of morpholinoglycine

A BODIPY-based fluorescent probe for the differential

5-Hydroxymethylcytosine-selective oxidation with peroxotungstate

Electronic Supplementary Information

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

Acid-Base Bifunctional Shell Cross-Linked Micelle Nanoreactor for One-pot Tandem Reaction

Discovery of Decamidine as a New and Potent PRMT1 Inhibitor

Linear Dependence of Water Proton Transverse Relaxation Rate on Shear Modulus in Hydrogels

Utilizing ELSD and MS as Secondary Detectors for Prep HPLC and Flash Chromatography. Tips and Techniques to Optimize ELSD and MS based Purification

Prep 150 LC System: Considerations for Analytical to Preparative Scaling

Supporting Information

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006

Aziridine in Polymers: A Strategy to Functionalize Polymers by Ring- Opening Reaction of Aziridine

Electronic Supplementary Material (ESI) for Medicinal Chemistry Communications This journal is The Royal Society of Chemistry 2012

Supporting Information. Light-Induced Hydrogen Sulfide release from Caged gem-dithiols

SUPPLEMENTARY INFORMATION

Supporting information

Supporting Information

Supporting Information. Enantioselective Organocatalyzed Henry Reaction with Fluoromethyl Ketones

ADVANTAME (TENTATIVE)

Electronic Supplementary Information

Supporting Information

Supplementary Note 2. Synthesis of compounds. Synthesis of compound BI Supplementary Scheme 1: Synthesis of compound BI-7273

Diastereospecific Enolate Addition and Atom- of L/T Calcium Channel Blocker ACT

In vivo monitoring of hydrogen sulfide using a cresyl violet-based ratiometric fluorescence probe

Department of Civil and Environmental Engineering, Stanford University, 473 Via Ortega, Stanford, California 94305, United States

with EDCI (5.73 g, 30.0 mmol) for 10 min. Bromoethylamine hydrobromide (6.15

Electronic Supplementary Information (ESI) for New Journal of Chemistry

Supporting Information

SUPPLEMENTARY INFORMATION

Supporting Information

SUPPLEMENTARY INFORMATION

Shodex TM ODP2 HP series columns

Supporting Information for

All solvents and reagents were used as obtained. 1H NMR spectra were recorded with a Varian

(Supplementary Information)

Transcription:

Supporting Information Copyright Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, 2007

Copyright Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, 2007 Supporting Information for Head-to-Tail Cyclized Cystine-Knot Peptides via a Combined Recombinant and Chemical Route of Synthesis Olga Avrutina, Hans-Ulrich Schmoldt, Dusica Gabrijelcic-Geiger, Alexander Wentzel, Holm Frauendorf, Christian P. Sommerhoff, Ulf Diederichsen and Harald Kolmar Reagents and solvents: All chemicals were of highest grade available and used as supplied. High performance liquid chromatography: HPLC was performed on a Pharmacia Äcta basic system (pump type P-900, variable wavelength detector, type UV-900) by using the following columns: Analytical HPLC: Preparative HPLC: YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 4 µm, 8 nm) Phenomenex Synergi 4u Hydro-RP 80 Å (250 4.6 mm, 4 µm, 8 nm) YMC J sphere ODS H-80, RP C-18 (250 20 mm, 4 µm, 8 nm) Phenomenex Synergi 4u Hydro-RP 80 Å (250 10 mm, 4 µm, 8 nm) - 1 -

HPLC runs were performed with the following eluents: A (0.1 % aq. TFA), B1 (90 % aq. acetonitrile, 0.1 % TFA), and B2 (100 % acetonitrile, 0.1 % TFA). Two gradients were used. Gradient 1: a) 10 % B2 (6 min), b) 10? 26 % B2 (6 min); c) 26? 30 % B2 (12 min); d) 30? 44 % B2 (6 min). Gradient 2: 10? 40 % B1 (30 min). For analysis and purification HPLC grade acetonitrile and millipore water were used. Flow rates were 1 ml/min for analytical (column 250 4.6 mm), 5 ml/min for semi-preparative (column 250 10 mm), and 10 ml/min for preparative purifications (column 250 20 mm). UV detection was performed at 215 nm for fully deprotected peptides and at 280 nm for the hydrazone-containing peptides to detect hydrazone formation. 1. McoEeTI SDG homoserine lactone (4) O H-SDGGVCPKILKKCRRDSDCLAGCVCGPNGFCGV NH O C 139 H 224 N 44 O 45 S 6 [3423.09] Barnase -McoEeTI fusion protein was dissolved in 0.2 M HCl/8 M urea and 0.6 µl of 5 M BrCN solution was added. After overnight incubation the sample was diluted 1:10 with eluent A containing 5 % acetonitrile and subjected to a XK26 column (Amersham Biosciences) containing Amberchrom CG-300M (Tosoh Bioscience, 100 ml bed volume). After washing with 0.1% Vol. aqueous TFA, the cleaved microprotein was separated from the barnase'-carrier using a gradient from 5 to 50% eluent B1 within 30 min. McoEeTI containing fractions were combined and lyophilized. Additional purification was performed by the preparative HPLC to give 6 mg of 4. Analytical data: HPLC (Figure S1): R t = 18.30 (gradient 1); MS (ESI): m/z: 856.9 [M + 4 H] 4+, 3424.49 [M + H] + ; HRMS (ESI): calcd for C 139 H 224 N 44 O 45 S 6 : 856.38019, 3421.49110, found 856.43374 [M + 4 H] 4+, 3421.49229 [M 0 ]. - 2 -

Figure S1. Analytical HPLC of 4 at 215 nm. Column - Phenomenex Synergi 4u Hydro-RP 80 Å (250 4.6 mm, 4 µm, 8 nm). 2. McoEeTI SDG hydrazide (6) H-SDGGVCPKILKKCRRDSDCLAGCVCGPNGFCGVHse-NHNH 2 C 139 H 228 N 46 O 45 S 6 [3456.2] Hydrazine hydrate (7 µl, 0.14 mmol) was added to McoEeTI SDG homoserine lactone 4 (4.7 mg, 1.4 µmol) solution in water (2 ml). The mixture was stirred for 1 h at room temperature. Reaction was monitored by analytical HPLC (Figure S2). The reaction mixture was lyophilized to remove the excess of hydrazine. The sample was redissolved in 10 % eluent B2 and purified by a preparative HPLC to yield 2.1 mg (44.3%) of 6. Peak at 16.06 min corresponds to a peptide with C-terminal Hse. (MS: calcd 3442.2; found m/z 861.5 [M + 4 H] 4+, 1148.0 [M + 3 H] 3+, 1185.0 [M + 3 H + TFA] 3+ ). Analytical data: HPLC (Figure S3): R t = 15.68 (gradient 1); MS (ESI): m/z: 864.8 [M + 4 H] 4+, 1152.9 [M + 3 H] 3+, 1190.0 [M + 3 H + TFA] 3+. - 3 -

Figure S2. Monitoring of hydrazinolysis of 4 at 215 and 280 nm. Reaction progress after 1 h. Column - Phenomenex Synergi 4u Hydro-RP 80 Å (250 4.6 mm, 4 µm, 8 nm). Figure S3. Analytical HPLC of 6 at 215 and 280 nm in phosphate buffer. Column - Phenomenex Synergi 4u Hydro-RP 80 Å (250 4.6 mm, 4 µm, 8 nm). - 4 -

3. cmcoeeti SDG (8) O DGGVCPKILKKCRRDSDCLAGCVCGPNGFCGVHse N NH C136H218N44O43S6 [3407.2] McoEeTI SDG hydrazide 6 (1.6 mg, 0.46 µmol) was dissolved in 1 ml 10 mm phosphate buffer ph 7.0. NaIO 4 (1 mg, 4.6 µmol) was added as a solution in phosphate buffer (1 ml). After 5 min at room temperature the reaction was terminated by HPLC injection. Monitoring was performed at 280 nm to detect macrocycle formation (Figure S4). Pure yield of 8 was 1 mg (63.7%). Analytical data: HPLC (Figure S5): R t = 19.23 (gradient 2); MS (ESI): m/z: 1136.5 [M + 3 H] 3+, 1173.6 [M + 3 H + TFA] 3+, 1704.3 [M + 2 H] 2+. Figure S4. Monitoring of sodium periodate oxidation-cyclization of 6 at 280 nm in phosphate buffer. Reaction progress after 5 min. Column - Phenomenex Synergi 4u Hydro-RP 80 Å (250 4.6 mm, 4 µm, 8 nm). - 5 -

Figure S5. Analytical HPLC of 8 at 215 and 280 nm. Gradient 2. Column - YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 4 µm, 8 nm). 4. McoEeTI KKV homoserine lactone (3) O H-SGVCPKILKKCRRDSDCLAGCVCGPNGFCGAKKV NH O C 148 H 246 N 46 O 42 S 6 [3534.28] McoEeTI KKV homoserine lactone was synthesized according to the method described in section 1. Additional purification was made by the preparative HPLC to give 8 mg of 3. Analytical data: HPLC (Figure S6): R t = 19.01 min (gradient 2); MS (ESI): m/z: 884.1 [M + 4 H] 4+, 3533.69 [M + H] + ; HRMS (ESI): calcd for C 148 H 246 N 46 O 42 S 6 : 883.92858, 3531.68520; found 883.92839 [M + 4 H] 4+, 3531.68199 [M 0 ]. - 6 -

Figure S6. Analytical HPLC of 3 at 215 nm. Gradient 2. Column - YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 4 µm, 8 nm). 5. McoEeTI KKV hydrazide (5) H-SGVCPKILKKCRRDSDCLAGCVCGPNGFCGAKKVHse-NHNH 2 C 148 H 250 N 48 O 42 S 6 [3566.32] Hydrazine hydrate (10 µl, 0.2 mmol) was added to McoEeTI KKV homoserine lactone 3 (7 mg, 2 µmol) solution in 2 ml 10 mm phosphate buffer (ph 6). The mixture was stirred for 1 h at room temperature. Reaction was controlled by analytical HPLC (Figure S7). After the starting lactone was completely consumed, the reaction mixture was lyophilized to remove the excess of hydrazi ne. The dry residue after lyophilization was re-dissolved in water-acetonitrile mixture and subjected to a preparative HPLC affording 4.5 mg (64.3%) of 5. Analytical data: HPLC (Figure S8) : R t = 16.92 (gradient 2); MS (ESI): m/z: 892.4 [M + 4 H] 4+, 1189.6 [M + 3 H] 3+, 3566.7 [M + H] +. - 7 -

Figure S7. Monitoring of hydrazinolysis of 3 at 215 nm in water. Reaction progress after 1 h. Gradient 2. Column - YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 8 nm). Figure S8. Analytical HPLC of 5 at 215 nm in phosphate buffer. Gradient 2. Column - YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 4 µm, 8 nm). - 8 -

6. McoEeTI KKV aldehyde (7) OHCCO-GVCPKILKKCRRDSDCLAGCVCGPNGFCGAKKVHse-NHNH 2 C 147 H 245 N 47 O 42 S 6 [3535.27] McoEeTI KKV hydrazide 5 (4 mg, 1.1 µmol) was dissolved in phosphate buffer 1 ml 10 mm phosphate buffer ph 7.0. NaIO 4 (2.4 mg, 11 µmol) was added as a solution in phosphate buffer (1 ml). After 5 min at room temperature the reaction was terminated by HPLC injection (Figure S9). Yield of 7 was 2.5 mg (62.8%). Analytical data: HPLC: R t = 18.55 min (gradient 2); MS (ESI): m/z: 3535.7 [M + H] +. Figure S9. Monitoring of sodium periodate oxidation of 5 at 215 nm in phosphate buffer. Reaction progress after 5 min. Gradient 2. Column - YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 8 nm). - 9 -

7. cmcoeeti KKV (9) O GVCPKILKKCRRDSDCLAGCVCGPNGFCGAKKVHse N NH C 147 H 243 N 47 O 41 S 6 [3517.25] cmcoeeti KKV aldehyde 7 (2 mg, 0.56 µmol) was dissolved in 1 ml of 0.25 M sodium acetate buffer (ph = 5) and incubated at room temperature. The reaction progress was monitored by analytical HPLC at 215 and 280 nm (Figure S10). After 72 h the reaction mixture was subjected to preparative HPLC to yield 0.5 mg (25 %) of cmcoeeti KKV hydrazone (9). Analytical data: HPLC (Figure S11): R t = 20.23 min (gradient 2); MS (ESI): m/z: 704.3 [M + 5 H] 5+, 880.1 [M + 4 H] 4+, 1173.2 [M + 3 H] 3+, 3518.7 [M + H] +. Figure S10. Monitoring of macrocyclization of 7 at 215 and 280 nm in sodium acetate buffer. Reaction progress after 72 h. Gradient 2. Column - YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 8 nm). - 10 -

Figure S11. Analytical HPLC of 9 at 215 nm. Gradient 2. Column - YMC J sphere ODS H-80, RP C-18 (250 4.6 mm, 4 µm, 8 nm). - 11 -