microcystin detection

54
MICROCYSTIN DETECTION MICROCYSTIN DETECTION

Upload: linus

Post on 29-Jan-2016

29 views

Category:

Documents


0 download

DESCRIPTION

MICROCYSTIN DETECTION. Introduction. A real problem …. Introduction. … with social implications …. “Un chien mort dans les Gorges du Tarn” Lozère online , 29 juin 2005 “L’eau des gorges du Tarn empoisonne les chiens” L’indépendant, 9 août 2005 “Morts mystérieuses dans le Tarn” - PowerPoint PPT Presentation

TRANSCRIPT

Page 1: MICROCYSTIN DETECTION

MICROCYSTIN DETECTIONMICROCYSTIN DETECTION

Page 2: MICROCYSTIN DETECTION

Introduction

A real problem…

Page 3: MICROCYSTIN DETECTION

… with social implications… “Un chien mort dans les Gorges du Tarn”

Lozère online, 29 juin 2005

“L’eau des gorges du Tarn empoisonne les chiens”L’indépendant, 9 août 2005

“Morts mystérieuses dans le Tarn”Nuovo , 17 août 2005

“Fin de l'énigme sur la mort des chiens dans les gorges du Tarn”

Le Nouvel Observateur, 5 août 2005

Introduction

Page 4: MICROCYSTIN DETECTION

TheThe “ “wonderfulwonderful” cyanobacteria blooms” cyanobacteria blooms

Grandview Garden Park, Beijing

Baltic sea

Introduction

Page 5: MICROCYSTIN DETECTION

What do microcystins do?What do microcystins do?

In animals: skin sensitisation, paralysis, In animals: skin sensitisation, paralysis, convulsions, liver damage, disorientation, convulsions, liver damage, disorientation, constipation, scours, abortion and death.constipation, scours, abortion and death.

In humans: skin and eye irritation, dermatitis, In humans: skin and eye irritation, dermatitis, gastroenteritis, diarrhoea and vomiting, nausea, gastroenteritis, diarrhoea and vomiting, nausea, headaches and even death.headaches and even death.

Introduction

Page 6: MICROCYSTIN DETECTION

Microcystin: heptapeptideMicrocystin: heptapeptideIntroduction

Microcystis aeruginosa

Page 7: MICROCYSTIN DETECTION

Detection methodsDetection methods

METHODMETHOD TECHNIQUETECHNIQUE ADVANTAGESADVANTAGES DRAWBACKSDRAWBACKS

BiologicalBiological Mice and cellsMice and cells Easy, low-costEasy, low-cost Ethical, non specific Ethical, non specific non-sensitivenon-sensitive

ChemicalChemical HPLC-UV, HPLC-UV, LCMSLCMS

Sensitive, Sensitive, specificspecific

Expensive, long, skilled Expensive, long, skilled personnelpersonnel

ImmunologicImmunologicalal

ELISA with Mab ELISA with Mab and Paband Pab

Fast, easy, Fast, easy, sensitive, sensitive, availableavailable

Cross-reactivityCross-reactivity

EnzymaticEnzymatic PP inhibitionPP inhibitionFast, easy, Fast, easy, sensitive, sensitive, robustrobust

Non-specific, other Non-specific, other inhibitorsinhibitors

Introduction

Page 8: MICROCYSTIN DETECTION

Our goalOur goal

MicrocystinsMicrocystins detection in drinking waterdetection in drinking water WHO: 1WHO: 1g/L microcystin-LRg/L microcystin-LR

Amperometric biosensorAmperometric biosensor

Cost-effective (SP), sensitive and reliable deviceCost-effective (SP), sensitive and reliable device

3 approaches: enzyme sensor, 3 approaches: enzyme sensor, immunosensor and aptasensorimmunosensor and aptasensor

Objective

Page 9: MICROCYSTIN DETECTION

Enzyme sensor strategyEnzyme sensor strategy

Page 10: MICROCYSTIN DETECTION

Locks and keysLocks and keysProtein Phosphatase : Protein Phosphatase :

production and purificationproduction and purification

Electrochemically active substrate after Electrochemically active substrate after dephosphorylationdephosphorylation

Protein Phosphatase immobilisation:Protein Phosphatase immobilisation: sol-gel, glutaraldehyde, PVA-SbQsol-gel, glutaraldehyde, PVA-SbQ

Biosensor developmentBiosensor development

Biosensor validationBiosensor validation

Objective

Page 11: MICROCYSTIN DETECTION

Protein PhosphatasesProtein PhosphatasesEnzymatic Activity Results

Ascorbic acid 2-phosphatep-Nitrophenol + colour at = 405nm

Protein Phosphatase

p-Nitrophenyl Phosphate

PP2A-Upstate: PP2A-Upstate: 1900 mU / mL1900 mU / mL

PP1-Biolabs:PP1-Biolabs: 1574 mU / mL1574 mU / mL

PP2A-GTP: PP2A-GTP: 1080 mU / mL1080 mU / mL

Page 12: MICROCYSTIN DETECTION

Ascorbic acid 2-phosphateAscorbic acid 2-phosphate

P OH

OH

O

Ascorbic acid 2-phosphate Ascorbic acidAscorbic Acid (red)

Protein Phosphatase

Ascorbic Acid (ox)e-

Ascorbic Acid 2-Phosphate +400mV

Electrochemical Results

Page 13: MICROCYSTIN DETECTION

Ascorbic acid (comm. or ALP)Ascorbic acid (comm. or ALP)

No fouling (CV/CA)

Electrochemical Results

Page 14: MICROCYSTIN DETECTION

Ascorbic acid (PP)Ascorbic acid (PP)

NOTHING...

Electrochemical Results

Page 15: MICROCYSTIN DETECTION

4-Methoxyphenyl phosphate4-Methoxyphenyl phosphate

Ascorbic acid 2-phosphate Ascorbic acid4-Methoxyphenol (red)

Protein Phosphatase

4-Methoxyphenol (ox)e-

4-Methoxyphenyl Phosphate

+350mV

NMR: Non-pure P OH

OH

O

Electrochemical Results

Page 16: MICROCYSTIN DETECTION

4-Methoxyphenol (comm. or ALP)4-Methoxyphenol (comm. or ALP)

Fouling (CV/CA)

Electrochemical Results

Page 17: MICROCYSTIN DETECTION

4-Methoxyphenol (PP)4-Methoxyphenol (PP)

NOTHING...

Electrochemical Results

Page 18: MICROCYSTIN DETECTION

Phenyl phosphatePhenyl phosphate

Ascorbic acid 2-phosphate Ascorbic acidPhenol

Protein Phosphatase

Quinonee-

Phenyl Phosphate +550mV

Electrochemical Results

Page 19: MICROCYSTIN DETECTION

Phenol (comm. or ALP)Phenol (comm. or ALP)

Fouling (CV/CA)

Electrochemical Results

Page 20: MICROCYSTIN DETECTION

Phenyl phosphate (PP)Phenyl phosphate (PP)

NOTHING...

Electrochemical Results

Page 21: MICROCYSTIN DETECTION

Naphthyl phosphateNaphthyl phosphate

Ascorbic acid 2-phosphate Ascorbic acid Naphthol (red)

Protein Phosphatase

Naphthol (ox)e-

Naphthyl Phosphate +200mV

Electrochemical Results

Page 22: MICROCYSTIN DETECTION

Naphthol (comm. or ALP)Naphthol (comm. or ALP)

Fouling (CV/CA)

Electrochemical Results

Page 23: MICROCYSTIN DETECTION

Naphthol (PP2A-Upstate)Naphthol (PP2A-Upstate)

PP2A recognises -NP by CV, but there is

fouling

PP2A = 9.1mU[-NP] = 3mM

Electrochemical Results

Page 24: MICROCYSTIN DETECTION

Naphthol (PP1-Biolabs)Naphthol (PP1-Biolabs)

PP1 recognises-NP by CA, but there is fouling

PP1 = 7.5 mU[-NP] = 10mM

E = +370mVt = 9min

116nA(blk: 5nA)

Electrochemical Results

Page 25: MICROCYSTIN DETECTION

p-p-AminophenylAminophenyl phosphate phosphate

Ascorbic acid 2-phosphate Ascorbic acidp-Aminophenol (red)

Protein Phosphatase

p-Aminophenol (ox)e-

p-Aminophenyl Phosphate +150mV

Electrochemical Results

Page 26: MICROCYSTIN DETECTION

p-p-AminophenolAminophenol (ALP) (ALP)

Instability

Electrochemical Results

Page 27: MICROCYSTIN DETECTION

p-Aminophenol (PP1-Biolabs)p-Aminophenol (PP1-Biolabs)

PP1 recognisesp-APP by CA,

but p-AP is unstable

PP1 = 10mU[p-APP] = 0.1mM

E = +150mVt = 15min

67nA(blk: 5nA)

Electrochemical Results

Page 28: MICROCYSTIN DETECTION

Catechyl monophosphateCatechyl monophosphate

Ascorbic acid 2-phosphate Ascorbic acidCatechol (red)

Protein Phosphatase

Catechol (ox)e-

Catechyl Monophosphate +40mV

NMR: Catechyl monophosphate P OH

OH

O

Electrochemical Results

Page 29: MICROCYSTIN DETECTION

CatecholCatechol (comm. or ALP) (comm. or ALP)

Fouling (CV/CA)

Electrochemical Results

Page 30: MICROCYSTIN DETECTION

Catechol (PP2A-Upstate)Catechol (PP2A-Upstate)

PP2A recognises CMP by CV, but there is fouling

PP2A = 13.6mU[CMP] = 0.5mM

Electrochemical Results

Page 31: MICROCYSTIN DETECTION

Catechol (PP1-Biolabs)Catechol (PP1-Biolabs)

PP1 recognises CMP by CA!!!,

but there is fouling

PP1 = 7.5mU[CMP] = 5mME = +450mV

t = 9min

Electrochemical Results

1383nA(blk: 395nA)

CMP + PP

blank

Page 32: MICROCYSTIN DETECTION

Natural susbstrates: peptidesNatural susbstrates: peptides

Ascorbic acid 2-phosphate Ascorbic acidRRACVA Peptide (red)

Protein Phosphatase

RRACVA Peptide (ox)e-

RRApCVA Peptide +500mV

Electrochemical Results

Ascorbic acid 2-phosphate Ascorbic acidRRAYVA Peptide (red)

Protein Phosphatase

RRAYVA Peptide (ox)e-

RRApYVA Peptide +550mV

DIFFICULT SYNTHESIS...

NOTHING...

Page 33: MICROCYSTIN DETECTION

Electrochemical substratesEnzyme sensor

P OH

OH

OCatechyl monophosphate

4-Methylumbelliferylphosphate

α-Naphthylphosphate

Page 34: MICROCYSTIN DETECTION

CV and amperometryEnzyme sensor

α-Naphthyl phosphate + PP: + 300 mV → 116 nA (blk: 23%)

Catechyl phosphate + PP: + 450 mV → 637 nA (blk: 5%)

4-Methylumbelliferyl phosphate + PP: + 700 mV → 429 nA (blk: 52%)

MUP + PP

blank

Page 35: MICROCYSTIN DETECTION

H3 CN+

O

OOH

OH

OH

OH

N+CH3

OO

OHOH

OHOH

PVA-SbQprepolymer

h ν

E

E

E

Y -N+CH3

OO

OHOH

OHOH

(Enzyme)

+ E E

PVA-SbQ entrapment method

Immobilisation Results

Page 36: MICROCYSTIN DETECTION

MC-LR detection (e-)Enzyme sensor

PP:PVA

3 h neon light1 day drying

4°C

Inhibition

30 min MCRT

Electrochemical detection

5mM CP+ 450 mV

C W R

IC50 = 8.30 μg/L

Page 37: MICROCYSTIN DETECTION

PP1α

• genetically engineered enzyme

• histidine tags

•selective towards MCs

The affinity of histidine residues for Ni precharged magnetic beads allows selective immobilisation of histidine fusion protein.

Page 38: MICROCYSTIN DETECTION

30 mg of PP1α

25 μL of mag-Ni-PP1α in 300 μL assay buffer

30 μL/SPE+160 μL of MC-LR

30’ incubation

+10 μL α-NPP

SPE

Chronoamperometry

Page 39: MICROCYSTIN DETECTION

MC-LR, ppb

1 10 100 1000

I, %

40

50

60

70

80

90

100

110

IC50=12 ppb

IC50=77 ppb

(M. Campàs et al., 2005)

PP1PP1αα BIOSENSOR BIOSENSOR

SPE

Page 40: MICROCYSTIN DETECTION

Random sequence

Constantregion

Constantregion

5’ 3’

ssDNA oligonucleotides

Combinatorial LibraryTarget

OTAMagnetic

Beads

Binding

Washing

Elution

AmplificationPCR

Purification of ssDNA

dsDNA

Enriched ssDNA pool

1. SELEXRound

2-n SELEXRound

Last SELEXRound

Cloning andSequencing

SELEXProcess

MB

MB

MB

MB

MB

Removal of unboundoligonucleotides

Page 41: MICROCYSTIN DETECTION

ImmunosensorImmunosensor strategystrategy

Page 42: MICROCYSTIN DETECTION

The “immuno” strategy

Screen-printed electrode

MC-enzymeconjugate

Enzyme product

Immunosensor

PAb/MAb

Enzyme substrate

MC

Page 43: MICROCYSTIN DETECTION

CheckerboardsImmunosensor

[MAb] = 1 µg/L [MC-LR-HRP]MAb = 195,0 µg/L

[PAb] = 1:2,750 [MC-LR-HRP]PAb = 277,5 µg/L

21,9 µg/L

23,5 µg/L

Page 44: MICROCYSTIN DETECTION

Competition optimisationImmunosensor

MC-LR-HRP incubation time: compromise betweenthe colorimetric response (from HRP) and the [MC]

2 h MC incubation + 30 min competition with MC-LR-HRP (90 µL of MC + 10 µL of MC-LR-HRP)

Page 45: MICROCYSTIN DETECTION

MC-LR detection (colour)

ELISA WELLS

IC50 (MAb) = 0.14 μg/L

IC50 (PAb) = 1.60 μg/L

SPEs

IC50 (MAb) = 0.28 μg/L

IC50 (PAb) = 1.81 μg/L

Immunosensor

Page 46: MICROCYSTIN DETECTION

Looking for a mediatorImmunosensor

Ferrocene carboxylic acid

o-Phenylene diamine (PDA)

Catechol

2,6-Dichlorophenol-indophenol (DPIP)

Os(2,2‘-bipyridyl)2Cl(4-(aminomethyl)pyridine)

7,7,8,8-Tetracyanoquinodimethane (TCNQ)

1-Methoxy-5-methyl-phenazinium methyl sulfate (MMPMS)

5-Methyl-phenazinium methyl sulfate (MPMS)

Page 47: MICROCYSTIN DETECTION

MPMSImmunosensor

MPMS + HRP + H2O2

MPMS Chronoamperometry

2 min substrate incubationEreading = - 0.2 V for 20 sec

Page 48: MICROCYSTIN DETECTION

MC-LR detection (e-)Immunosensor

MPMS in solution

Total system for MAb: 5441 ± 542 nA (10.0 %)

Total system for PAb: 5698 ± 675 nA (11.9 %)

No Ab: 4595 ± 362 nA (7.9 %)No MC-LR-HRP: 4400 ± 342 nA (7.8 %)No H2O2: 2901 ± 115 nA (4.0 %)No MPMS: 1026 ± 183 nA (17.8 %)

IC50 (MAb) = 0.02 μg/L

IC50 (PAb) = 1.73 μg/L

19 % for MAb

15 % for PAb

of MC-LR-HRP

non-specific

adsorption

1041

1298

Page 49: MICROCYSTIN DETECTION

Looking for an immobilised mediator

Immunosensor

Ferrocene-COOH

Catechol

1-Methoxy-5-methyl-phenazinium methyl sulfate (MMPMS)

Prussian Blue (PB)

Meldola Blue Reinecke salt (MBRS)

Os “wire”

Cobalt phthalocyanine

7,7,8,8-Tetracyanoquinodimethane (TCNQ)

Page 50: MICROCYSTIN DETECTION

TCNQImmunosensor

Chronoamperometry

2 min substrate incubationEreading = - 0.2 V for 20 sec

TCNQ + HRP + H2O2

TCNQ

Page 51: MICROCYSTIN DETECTION

MC-LR detection (e-)Immunosensor

Immobilised TCNQ

Total system for MAb: 2404 ± 172 nA (7.2 %)

Total system for PAb: 2770 ± 399 nA (14.4 %)

No Ab: 2021 ± 152 nA (7.5 %)No MC-LR-HRP: 1912 ± 196 nA (10.3 %)No H2O2: 448 ± 43 nA (9.6 %)No TCNQ: 802 ± 61 nA (7.6 %)

22 % for MAb

13 % for PAb

of MC-LR-HRP

non-specific

adsorption

IC50 (MAb) = 0.46 μg/L

IC50 (PAb) = 1.66 μg/L

492

858

Page 52: MICROCYSTIN DETECTION

Aptasensor strategyAptasensor strategy

Page 53: MICROCYSTIN DETECTION

Aptasensor

Screen-printed electrode

Biotinylatedaptameragainst MC

Enzyme substrate

Enzyme product

MC-enzymeconjugate

Streptavidinor avidin

Aptasensor schemeAptasensor scheme

Page 54: MICROCYSTIN DETECTION

Random sequence

Constantregion

Constantregion

5’ 3’

ssDNA oligonucleotides

Combinatorial LibraryTarget

OTAMagnetic

Beads

Binding

Washing

Elution

AmplificationPCR

Purification of ssDNA

dsDNA

Enriched ssDNA pool

1. SELEXRound

2-n SELEXRound

Last SELEXRound

Cloning andSequencing

SELEXProcess

MB

MB

MB

MB

MB

Removal of unboundoligonucleotides