Chemical Biology of Cellular Carbohydrates · Metabolic Glycoengineering with Carbamates Ac...
Transcript of Chemical Biology of Cellular Carbohydrates · Metabolic Glycoengineering with Carbamates Ac...
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Universität Konstanz
Chemical Biology of Cellular Carbohydrates
Valentin WittmannUniversität Konstanz
XVIIth Ischia Advanced School of Organic Chemistry (IASOC Conference), Ischia, 28.09.2016
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PosttranslationalModification
(Glycosylation,Phosphorylation,Ubiquitination,Acetylation,Methylation, ...)
Glycoprotein
Central Dogma of Molecular Biology
DNA RNA ProteinTranscription Translation
Retroviruses
Splicing/Processing
Replication
It has been estimated that more than 50% of all proteins are glycosylated.R. Apweiler, H. Hermjakob, N. Sharon, Biochim. Biophys. Acta 1999, 1473, 4-8.
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Common Classes of Glycoconjugates
S. S. Pinho, C. A. Reis, Nat. Rev. Cancer 2015, 15, 540
1. Mechanistic investigation of carbohydrate-lectin interactions
2. Tracing carbohydrates in living cells
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Carbohydrate-Lectin Interactions
E-selectin • sLex
KD 700 Mgalectin-1 • LacNAc
KD 91 M
Con A • Man(1-2)ManKD 24 M
1I3H
Lec B (PA-IIL) • FucKD 2.9 M
1G1T 1W6P
1GZT
Increased binding affinity through
Multivalency
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Multivalent Carbohydrate-Lectin Interactions
V. Wittmann, R. J. Pieters, Chem. Soc. Rev. 2013, 42, 4492
• Increased affinity even if spacer is too short
• Binding modes?
Strong interest in understanding the molecular mechanisms of multivalency
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Model Lectin: Wheat Germ Agglutinin (WGA)
• Chitin-binding lectin from Triticum vulgaris
• Stable homo dimer: 2 x 171 amino acids
• 8 Binding sites per dimer(4 ‘primary’ and 4 ‘secondary’)
• Carbohydrate ligand:
OOH
NHAcHO
HOOH
OOH
NHAcHOO
OH
AcHNHOO O
OHH
n
and
GlcNAcKd: 1–5 mM
Chitobiose (n = 1)Kd: 50–200 M
WGA • GlcNAc (PDB ID: 2UVO)
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Angew. Chem., Int. Ed. 2000, 39, 4348Angew. Chem., Int. Ed. 2004, 43, 900
Spatial Screening of Wheat Germ Agglutinin (WGA) Ligands
Rn = amino acid side chainor
J. Am. Chem. Soc. 2010, 132, 8704
1.83 mM (1)
NH
O
HNNH
NH2
O OO
HN
HNO
ONHO
NH
OHN
HN O
HN
O
Boc
NH
OHO
AcHN
OHHO
O
O
HN
OHO
AcHN
OHHO
O
O
OHO
AcHN
OHHO
OO
NH
HN
O
OHOH
O
O
AcHNOH
8.4 nM (218 000)
Absolute (and relative) KD values from ITC
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1.7 Å Structure of WGA 3 in Complex with Divalent Ligand
• 4 molecules of divalent ligand span pairs of binding sites.
• For the first time, all 8 binding sites are simultaneously occupied.
• Increased binding affinity of the divalent ligand allows identification of secondary binding sites.
J. Am. Chem. Soc. 2010, 132, 8704
(PDB ID: 2X52)
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2.75 Å Structure of Complex with Tetravalent Cyclic Peptide
1.44 M (1 270)
8.4 nM (218 000)
• two WGA dimers in asymmetric unit
• 11 out of 16 binding sites occupied
• remaining sites obstructed by crystal contacts
J. Am. Chem. Soc. 2010, 132, 8704
(PDB ID: 2X3T)
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90°
Joha
nnes
Bec
k, H
eiko
Möl
ler
Ensemble of the dominant family of conformers of the tetravalent neoglycopeptide determined by NMR spectroscopy
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Superposition of NMR and X-ray Structure
Backbone structure resolved in the crystal fits very well to the dominant conformational family determined by solution NMR.
J. Am. Chem. Soc. 2010, 132, 8704
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Absolute (and Relative) KD Values from ITC
NH
O
HNNH
NH2
O OO
HN
HNO
ONHO
NH
OHN
HN O
HN
O
Boc
NH
OHO
AcHN
OHHO
O
O
HN
OHO
AcHN
OHHO
O
O
OHO
AcHN
OHHO
OO
NH
HN
O
OHOH
O
O
AcHNOH
HN
ONH
O HN
ONH
O HN
ONH
ONH2
O
NH NH
NHNH
O
O
O
AcHN
OHHO
HOO
O
O
AcHN
OHHO
HO
O
AcHN O
HOHO
HO
O
O
AcHN O
HOHO
HO
O
8.4 nM (218 000)n = 0.84
7.0 nM (261 000)n = 0.95
6.2 nM (295 000)n = 0.86
Cross-linking(precipitate formation)
P. Rohse, V. Wittmann, Chem. Eur. J. 2016, 22, 9724-9733
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Absolute (and Relative) KD Values from ITC
NH
O
HNNH
NH2
O OO
HN
HNO
ONHO
NH
OHN
HN O
HN
O
Boc
NH
OHO
AcHN
OHHO
O
O
HN
OHO
AcHN
OHHO
O
O
OHO
OHHOHO
OO
NH
HN
O
OHOH
O
O
OH
OH
O NH
O HN
ONH
O HN
ONH
O HN
ONH
O HN
ONH
O
NH2
O
NH NH
NHNH
O
O
OOHHO
HOHO
O
O
O
AcHN
OHHO
HO
O
AcHN O
HOHO
HO
O
OOH
O
HOHO
HO
O
HN
ONH
O HN
ONH
O HN
ONH
ONH2
O
NH NH
NHNH
O
O
OOHHO
HOHO
O
O
O
AcHN
OHHO
HO
O
AcHN O
HOHO
HO
O
OOH
O
HOHO
HO
O
1.43 M (1 280)n = 1.81
1.25 M (1 460)n = 1.82
0.85 M (2 150)n = 2.01
P. Rohse, V. Wittmann, Chem. Eur. J. 2016, 22, 9724-9733
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DLS Measurements
• Measurement of scattered light• Influenced by speed of Brownian motion
of particles in solution Size of particles can be determined
Hydrodynamic radius
P. Rohse, V. Wittmann, Chem. Eur. J. 2016, 22, 9724-9733
Molecular weight (calculated)
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Plausible Binding Modes
P. Rohse, V. Wittmann, Chem. Eur. J. 2016, 22, 9724-9733
Divalent Ligands Tetravalent Ligands
L : P2 : 1
L : P1 : 1
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Multivalent Carbohydrate-Lectin Interactions
K: microscopic intermolecular association constantEM: microscopic effective molarity
C. A. Hunter, H. L. Anderson, Angew. Chem., Int. Ed. 2009, 48, 7488V. Wittmann, Curr. Opin. Chem. Biol. 2013, 17, 982
Concentration dependence
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S1
rAB
B0
2
203
13cos 14
A B edd
AB
g gr
S2Dipolar interaction contains information about the distance rAB between two coupled spins S1 and S2
EPR-Spectroscopy: Distance Measurements in (Frozen Glassy) Solution
Angew. Chem., Int. Ed. 2011, 50, 8428
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EPR-Derived Distance Distributions
1 2 3 4 5 6r [nm]
2.2 nm
4.2 nm
2.3 nm
1.8 nm
Ligand + WGA 4:1
Ligand + WGA 1:8
Ligand in solution
Ang
ew. C
hem
., In
t. E
d. 2
011,
50,
842
8
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EPR-Derived Distance Distributions
1.8 nm
Ligand in solution
1 2 3 4 5 6r [nm]
Ligand + WGA 1:8
3.1 nm
Ang
ew. C
hem
., In
t. E
d. 2
011,
50,
842
8
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EPR-Derived Distance Distributions
1 2 3 4 5 6
2.3 nm
r [nm]
Ligand + WGA 1:1
Ligand + WGA 7:1
Angew. Chem., Int. Ed. 2011, 50, 8428
HN
O
OHOHO
AcHNO
NO
NHO
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Protein Labeling: GFP Fusion Proteins
Green Fluorescent Protein (GFP)
NH
HO HN
O
O
NH OH
OHO
O
NH OH
OHNN
OH
cyclization
HO
O
NH OH
ONN
aerialoxidation
HO
O
NH OH
ONN
– H2OSer65
Tyr66Gly67
2008 Nobel Prize in ChemistryMartin ChalfieOsamu ShimomuraRoger Y. Tsien
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Metabolic Glycoengineering (MGE)
OAcO
HNAcOAcO
OAc
OX
O
COOH
OHO
HO
OH OH
NH
OX
glycanbiosynthesis
OCOOH
OHO
HOOH
OHNH
O
YXY
Probe Probe
ManNAc derivatives sialic acids bound to O- and N-glycans
GlcNAc derivatives O-GlcNAc
GalNAc derivatives mucin-type O-glycans
Interconversion can occur (catalyzed by epimerases).
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Metabolic Glycoengineering (MGE)
OAcO
HNAcOAcO
OAc
OX
O
COOH
OHO
HO
OH OH
NH
OX
glycanbiosynthesis
OCOOH
OHO
HOOH
OHNH
O
YXY
Probe Probe
Challenges
• Simultaneous detection of two (or more) different sugars
• Detection of glycans inside living cells
• Protein-specific detection of glycosylation
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Bioorthogonal Ligation Reactions for MGE
10–5 10–4 10–3 10–2 10–1 1 101 102 103 104 105
Staudinger ligation
CuAAC
+
NNN
OO
R RN3SPAAC
Rate constant / M–1s–1
Staudinger SPAAC CuAAC
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Inverse-Electron-Demand Diels-Alder (DAinv) Reaction
Carboni & Lindsey 1959, Sauer 1962
LUMO
HOMO
LUMO
HOMO
E
diene dienophile
2008: First application to bioconjugation
Braun/Wiessler: Drug Des. Dev. Ther. 2008, 2, 289Fox: J. Am. Chem. Soc. 2008, 130, 13518Weissleder/Hilderbrand: Bioconjugate Chem. 2008, 19, 2297
very fast irreversible metal-free bioorthogonal
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Spac
er
Spa c
e rChem. Eur. J. 2012, 18, 6548
Application of the DAinv Reaction for Bioconjugation
Chem. Commun. 2014, 50, 10827
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Dienophiles for the DAinv Reaction
10–5 10–4 10–3 10–2 10–1 1 101 102 103 104 105
Rate constant / M–1s–1
inverse-electron-demand Diels-Alder reaction
Staudinger SPAAC CuAAC
R
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Metabolic Glycoengineering with the DAinv Reaction
Angew. Chem., Int. Ed. 2013, 52, 4265
OAcO
HNAcOAcO
OAc
O
O
COOH
OHO
HO
OH OH
NH
O
glycanbiosynthesis
OCOOH
OHO
HOOH
OHNH
O
n
nNN
NN
R
NN
R n
Probe Probe
–N2
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Metabolic Glycoengineering with the DAinv Reaction
Control (no sugar)
Fluorescence images of living HEK 293T cells
Cells grown with 100 µM sugar for 2 days, incubated with Tz-biotin, and then AlexaFluor®647-streptavidin
Ac4ManNPtl
Ac4ManNHxl Sca
le b
ar: 3
0 m
Angew. Chem., Int. Ed. 2013, 52, 4265Tz-biotin
k = 0.021 M–1s–1
k = 0.041 M–1s–1
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Metabolic Glycoengineering with Carbamates
Ac4ManNPeocAc4ManNAloc Ac4ManNHeocAc4ManNBeoc
Control(no sugar)
Fluorescence images of living HEK 293T cells
Sca
le b
ar: 3
0 m
Chem. Eur. J. 2014, 20, 16502
0.0015 M–1s–1 0.014 M–1s–1 0.017 M–1s–1 0.074 M–1s–1
metabolic incorporation DAinv reactivity
Cells were grown with 100 µM sugar for 2 days, then incubated with Tz-biotin (1 mM, 6 h, 37 °C) and Alexa-Fluor®647-streptavidin (20 min, 37 °C).
k2:
50 % 13 % 6 % n/d
... and Jeremias Dold
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DMB Labeling of Released Sialic Acids
Ac4ManNAloc
Ac4ManNBeoc
50 %
13 %
Jeremias Dold
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Accelerating the DAinv Reaction
k = 0.137 M–1s–1 k = 13 M–1s–1
Devaraj group, Angew. Chem., Int. Ed. 2012, 51, 7476
Devaraj groupChemBioChem 2013, 14, 205
Wittmann groupBioconjugate Chem. 2014, 25, 147
See also: J. A. Prescher, Mol. BioSyst. 2014, 10, 1693
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Dual-Labeling Strategy (HEK 293T Cells)
Bioconjugate Chem. 2014, 25, 147
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Dual-Labeling Strategy (HEK 293T Cells)
Bioconjugate Chem. 2014, 25, 147
OAcO
HNAcOAcO
OAc
O
O
Control (no sugar)
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Visualization of Protein-Specific Glycosylation in Living Cells
Cy3-Tz (reacts more specific)
ON N
ONHN
N
NN
COO
TAMRA-Tz (cell-permeable)
Detection of FRET with high contrast even in presence of a large excess ofacceptor fluorophores by fluorescence lifetime imaging microscopy (FLIM)
Proteins of interest (POI): O-GlcNAc transferase (OGT), forkhead transcription factor Foxo1, tumor suppressor p53, serine/threonine kinase Akt1
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Fluorescence Lifetime Imaging Microscopy (FLIM)
The fluorescence lifetime is the average time that a molecule spends in the excited state.
J. R. Lakowicz et al., Biophys. J. 1984, 46, 463-477
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Visualization of O-GlcNAcylation of OGT inside Living Cells
F. Doll, A. Buntz, A.-K. Späte, V. F. Schart, A. Timper, W. Schrimpf, C. R. Hauck, A. Zumbusch, V. Wittmann, Angew. Chem. Int. Ed. 2016, 55, 2262-2266
HEK293T cells were transfected with OGT-EGFP or EGFP constructs and treated with Ac4GlcNAc (–) or Ac4GlcNCyoc (+) for 20 h.
Western blot analysis after immuno-precipitation using an anti-GFP antibodyand labeling with Cy3-tetrazine.
Representative fluorescence modulationlifetime images of individual cells afterlabeling with TAMRA-tetrazine.
10 µm
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Visualization of Protein-Specific Glycosylation in Living Cells
O-GlcNAcylation of Foxo1, p53, and Akt1 visualized by FLIM-FRET microscopy of individual cells
10 µm
F. Doll, A. Buntz, A.-K. Späte, V. F. Schart, A. Timper, W. Schrimpf, C. R. Hauck, A. Zumbusch, V. Wittmann, Angew. Chem. Int. Ed. 2016, 55, 2262-2266
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AcknowledgementThe groupOliver BaudendistelMonica BoldtJeremias DoldRaphael FahrnerRebecca FaißtJessica PfotzerPhilipp RohseOliver RudolphiVerena SchartMarkus SchöweDavid StängleMichael VoggelDaniel WielandIvan Zemskov
Former group membersDr. Ellen BatroffDr. Henning BeckmannDr. Carline MaierhoferDr. Andrea NiederwieserDr. Anne-Katrin-Späte
CooperationProf. Dr. Malte Drescher, Patrick Braun (U Konstanz, Chemistry)Prof. Dr. Wolfram Welte, David Schwefel (U Konstanz, Biology)Prof. Dr. Andreas Zumbusch, Franziska Doll (U Konstanz, Chemistry)Prof. Dr. Andreas Marx (U Konstanz, Chemistry)Prof. Dr. Thomas U. Mayer (U Konstanz, Biology)Prof. Dr. Christof Hauck (U Konstanz, Biology)Prof. Dr. W. Reutter (FU Berlin)Prof. Dr. H. Scherer (FU Berlin)Prof. Dr. G. Mayer (U Bonn)
Proto Chemicals AG
SFB 969
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Acknowledgement