A Rational Approach to Identification of Wild Type Trans-sialidases for the Production of Human Milk Oligosaccharides By Rune Thorbjørn Nordvang BioEng.

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Presentation transcript:

A Rational Approach to Identification of Wild Type Trans-sialidases for the Production of Human Milk Oligosaccharides By Rune Thorbjørn Nordvang BioEng Institute for Chemical and Biochemical Engineering Technical University of Denmark Glycobiology World Congress August 11 th 2015 Philadelphia

Outline Human Oligo Saccharides - structures and properties The BioEng HMO production setup (for sialyllated HMOs) In silico Trans-sialidase discovery – Strategy development – In silico results In vitro verification – Experimental – In vitro results Conclusions & Perspectives

HMO blueprint and selected HMO structures Bode L Glycobiology 2012;22: © The Author Published by Oxford University Press. All rights reserved. For permissions, please

Bode L Glycobiology 2012;22: © The Author Published by Oxford University Press. All rights reserved. For permissions, please Enzyme-catalysed synthetic HMO production setup

cGMP Figure adapted from: Zeuner B, et al Enzyme and Microbial Technology 55:85-93 Enz.

One native trans-sialidase is known TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784

The trans-sialidase of Trypanosomas cruzi TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784

The trans-sialidase of Trypanosomas cruzi TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784 Not a sialyl-transferase Virulence factor in a human pathogen

A quintuple mutant of it’s close cousin from the non-pathogenic T. rangeli

Tr13 Directed evolution

Compared to M. viridifaciens No trans-sialidase activity observed… …From a pupulation of more than 200 constructed mutants Jers C, et al. Oxford jour. doi: / protein/gzu054

All avancements based on TcTS New knowledge about trans-sialidases needed. No trans-sialyllation screening assays. Hard to find conserved AA when TcTS is the only trans-sialidase. What to do?

Hydrophobic pocket Conserved sialidase active site Conserved sialidase active site TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784 Reaquaint with TcTS

Hydrophobic pocket Conserved sialidase active site Conserved sialidase active site Hypothesis 1: The family of sialidases is extremely conserved and it can be speculated that a trans-sialidase could have developed in parallel with the TcTS inferring an aromatic sandwich in a similar position as it is found in TcTS. TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784 Enzyme identification strategy development

Hydrophobic pocket Conserved sialidase active site Conserved sialidase active site Hypothesis 2: If hypothesis 1 is correct, sialidases with an aromatic sandwich above the active site will be a good candidates for identifying sialidases with trans-activity. TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784 Enzyme identification strategy development

TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784 Hydrophobic pocket Conserved sialidase active site Conserved sialidase active site Search for motif: [W/Y/F-x-R-D-R] Enzyme identification strategy development

A closer look at the TcTS active site TcTS model based on Amaya M.F., et.al. (2004) Structure 12: 775–784

Candidate selection 3D homology moddeling using HHpred and CPHmodels Alignment of active site residues Visual inspection Aligned active site residues for 1 of 15 candidate enzymes

4 candidates enzymes model and align well

4 candidate enzymes selected for in vitro analysis

Candidate alignment overview

One candidate stands out

The remaining 3 candidates included - Deep narrow binding pockets

Enzyme expression setup Gene sequences synthesized (DNA2.0) – With N-terminal His-taq – T7 promotor expression system vector Transformed into E. coli BL2 (DE3) Overnight 30ᵒ C autoinduction expression Enzyme recovery – Sonication – Äkta purification

Applying the candidate enzymes to the trans-sialidase setup cGMP Figure adapted from: Zeuner B, et al Enzyme and Microbial Technology 55:85-93 Enz.

cGMP Figure adapted from: Zeuner B, et al Enzyme and Microbial Technology 55:85-93 Enz. Reaction conditions Volume: 1ml (Eppendorf tubes) Lactose: 100 g/L cGMP: 40 g/L Temperature: 30 O C (Thermo mixer) pH:6.4 Mixing:700 rpm (Thermo mixer) Reaction stop:Heat inactivation 10 min. Reaction time:2 hours

HPLC - Analysis Sial A Type: HPAEC-PAD Column:CarboPac TM PA100 Machine: ICS 3000 (Dionex Corp., Sunnyvale, CA) Hydrolase/Sialidase

HPLC - Analysis Sial A Sial H Hydrolase/Sialidase

Sial A Sial H Sialic acid Sialyllactose Hydrolase/Sialidase HPLC - Analysis

Sial A Sial H Hydrolase/Sialidase Trans-activity!!! Sialic acid Sialyllactose HPLC - Analysis

Sial A Sial H Sialic acid Sialyllactose Mystery peak 2 HPLC - Analysis

Product identification 3-sialyllactose MS and β-galactosidase treatment Confirmed by NMR

Time study SialH Products 3’SL and 3SL reaches levels of 1.5 mM and 0.9 mM respectively SA 3’SL 3SL 6’SL

Time study (all candidates) SA 3’SL 3SL 6’SL SA

Time Study (all candidates)

Conclusion ”We give to you”

Conclusion The trans-sialidase of Haemophilus parasuis (HpTS)

Conclusion Novel trans-sialidase identified -From a database of 2909 sialidases -Identified by rational sequence analysis strategy -First confirmed bacterial trans-sialidase -Trans-sialidase of H. parasuis Novel sialylation product identified -New type of 3-sialyllactose 4 candidates showed trans-activity -Although higher hydrolysis rates were observed

Novel trans-sialidase identified -From a database of 2909 sialidases -Identified by rational sequence analysis strategy -First confirmed bacterial trans-sialidase -Trans-sialidase of H. parasuis Novel sialylation product identified -New type of 3-sialyllactose 4 candidates showed trans-activity -Although higher hydrolysis rates were observed < Conclusion Hypothesis 1: The family of sialidases is extremely conserved and it can be speculated that a trans-sialidase could have developed in parallel with the TcTS inferring an aromatic sandwich in a similar position as it is found in TcTS. Hypothesis 2: If hypothesis 1 is correct, sialidases with an aromatic sandwich above the active site will be a good candidates for identifying sialidases with trans-activity.

Novel trans-sialidase identified -From a database of 2909 sialidases -Identified by rational sequence analysis strategy -First confirmed bacterial trans-sialidase -Trans-sialidase of H. parasuis Novel sialylation product identified -New type of 3-sialyllactose 4 candidates showed trans-activity -Although higher hydrolysis rates were observed < Conclusion Hypothesis 1: The family of sialidases is extremely conserved and it can be speculated that a trans-sialidase could have developed in parallel with the TcTS inferring an aromatic sandwich in a similar position as it is found in TcTS. Hypothesis 2: If hypothesis 1 is correct, sialidases with an aromatic sandwich above the active site will be a good candidates for identifying sialidases with trans-activity.

Perspectives Crystallography of HpTS – Common traits between TcTS and HpTS – Further improvement of Tr13? – Identification of more native trans-sialidases Identification of other trans-glycosidases – ”Where can I find a sandwich ?”

Acknowledgements Colleagues: Arla Foods A.M.B.A for providing substrate for donating the trans-sialylation reaction substrates PhD C. Jers PhD J. Holck PhD M. Lezyk PhD C. NyffeneggerPhD B. Zeuner PhD Candidate S Jamek Prof AS Meyer (Supervisors) Prof JD Mikkelsen Asst Prof M. Pinelo

Questions please Thank you for your attention