dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

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Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides Steen Brøndsted Nielsen Department of Physics and Astronomy University of Aarhus June 24-27, 2004, Lyon-France

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Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides Steen Brøndsted Nielsen Department of Physics and Astronomy University of Aarhus. June 24-27, 2004, Lyon-France  . DNA DAMAGE. HOW DOES UV RADIATION CAUSE GENETIC DAMAGE ?. - PowerPoint PPT Presentation

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Page 1: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

Steen Brøndsted Nielsen

Department of Physics and Astronomy

University of Aarhus

June 24-27, 2004, Lyon-France 

Page 2: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

DNA DAMAGE

Page 3: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

HOW DOES UV RADIATION CAUSE GENETIC DAMAGE ?

1) Direct absorption of light by the nucleobases

followed by physical and chemical reactions

and / or

2) Ionisation of water (H2O H2O+ + e) followed

by electron attachment to nucleobases

Modification of nucleobases may lead to loss of base-pairing specificity

Page 4: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

Elucidate the processes at the single-molecule level.

Isolated damage to nucleotides, the basic building blocks of DNA and RNA, upon electron attachment.

OUR APPROACH

Page 5: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

TOOLBOX

ELECTROSPRAY IONISATION

MASS SPECTROMETRY:

ACCELERATOR INSTRUMENT

ION STORAGE RING ELISA

LASERS

QUANTUM CHEMICAL CALCULATIONS

Page 6: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

BARE IONS

ELECTROSPRAY IONISATION

droplets

Page 7: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

ELECTROSPRAY ION SOURCE

1 mbar 10-3 mbar 10-5 mbar 10-6 mbar

Heatedcapillary

ESI needle4kV

22-pole ion trap

Tube lensSkimmer

OctapoleLenses

Acceleration tube

Page 8: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

GAS-PHASE EXPERIMENTS ON NUCLEOTIDE ANIONS

PROBLEM:

Attachment of an electron to a negative

ion is unlikely because of the repulsion

between the two negative charges.

SOLUTION:

High-energy collisions with sodium:

electron transfer from Na to the ion.

R 0

dianion

Ener

gy

Anion - electron distance R

dianion

Compare: the violent reaction of sodium with water !

Nielsen et al., J. Am. Chem. Soc. 125, 9592-9593 (2003).

Liu et al., Chem. Phys. Chem. 4, 1341-1344 (2003).

Page 9: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

ACCELERATOR INSTRUMENT

ESIsource

Magnet

Na collision cell

Electrostaticanalyser

0 V

50 kVChanneltron

detector

+

R = 2 mB = 1.4 T

T=500 K

Page 10: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

COLLISION INTERACTION TIME: FEW FEMTOSECONDS

Na

-Nucleotide anion

105 m/s

1 nm

The electron transfer process is nearly vertical.

Page 11: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

Electron attachment to AMP anions

O

OH OH

N N

N N

NH2

CH2O

O

P

O

OH

1

2

34

567

8

9

1'2'3'

4'

5'

m/q 346

Ne

Na

Liu et al., Chem. Phys. Chem. 4, 1341-1344 (2003).

80 120 160 200 240 280 320 360

dianion[AMPAH] [AMPO]

AMP

A

H2PO4

PO3

AMP

[AMPAH]A

H2PO4

PO3

m/q

Page 12: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

164 166 168 170

High-energy collisions between dAMP anions and Na and Ne

100 150 200 250 300

m/q

dAMPdAMP2

fragment ions m/q 330

Page 13: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

Spectrum obtained after collisions between AMP(H2O)13 and Na

100 200 300 400 500 600

m/q

170 190 210 230 250

AMP(H2O)13

AMP2 AMP2(H2O)9

AMP

Page 14: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

100 200 300 400 500 600

m/q

dG2

dT2

dC2

dA2

Electron transfer from Na to dinucleotide anions

sugar

sugar

phosphate

nucleobase

nucleobase

dianion

-

Page 15: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

IS THE NUCLEOTIDE DIANION INTACT ?

H loss is observed upon electron attachment to nucleobases in vacuo.

C. Desfrancois, H. Abdoul-Carime, and J. P. Schermann, J. Chem. Phys. 104, 7792 (1996).S. Gohlke, H. Abdoul-Carime, and E. Illenberger, Chem. Phys. Lett. 380, 595 (2003). G. Hanel, B. Gstir, S. Denifl, P. Scheier, M. Probst, B. Farizon, M. Farizon, E. Illenberger, and T. D. Märk, Phys. Rev. Lett. 90, 188104 (2003). H. Abdoul-Carime, S. Gohlke, and E. Illenberger, Phys. Rev. Lett. 92, 168103 (2004).

H loss is observed upon electron attachment to deoxyribose in vacuo.

S. Ptasińska, S. Denifl, P. Scheier, and T. D. Märk, J. Chem. Phys. 18, 8505 (2004).

Page 16: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

1.5 1 0.5 0m/q

# of D in AMP

0

1

2

3

Intact dianion H D

AMP dissolved in CD3OD:

Selection of deuterium-labelled ions for collision experiments

O

OH OH

N N

N N

NH2

CH2O

O

P

O

OH

1

2

34

567

8

9

1'2'3'

4'

5'

Exchangeable hydrogens

Liu et al., J. Chem. Phys., issued for Sept. 1 (2004).

Page 17: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

WHAT IS THE ORIGIN OF THE HYDROGEN ?

POH phosphoric acid group

OH sugar

NH2 nucleobase

CH sugar or nucleobase

Page 18: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

Electron attachment to nucleotides:

dehydrogenation at nitrogen sites

NNH

O

OCH3

NNH

O

O

Thymine Uracil Adenine Cytosine Guanine

N N

N N

NH2

NN

O

NH2

N N

N NH

O

NH2

1 2 3

Page 19: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

0 1 2 30.0

0.1

0.2

0.3

0.4

2 )

Number of nitrogen hydrogens

RNA nucleotide DNA nucleotide

Cross section for formation of dehydrogenated dianion

Page 20: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

• H-loss from N

• No D-loss from C

H. Abdoul-Carime, S. Gohlke, and E. Illenberger, Phys. Rev. Lett. 92, 168103 (2004).

Dissociative electron attachment to deuterated thymine

Page 21: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

THE DNA DOUBLE HELIX

Page 22: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

Watson-Crick base pairs Base mispairing

Biological relevance?

Page 23: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

WHAT IS THE LIFETIME OF THE DIANION ?

Page 24: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

1 mMicro-channel platedetector

Accelerator with electrospray ion source

Magnet

Ion bunch

Injection

ELectrostatic Ion Storage Ring Aarhus (ELISA)

S.P. Møller, NIM A 394, 281 (1997).

J.U. Andersen, J.S. Forster, P. Hvelplund, T.J.D. Jørgensen, S.P Møller, S. Brøndsted Nielsen, U.V. Pedersen, S. Tomita, and H. Wahlgreen, Rev. Sci. Instrum. 73, 1284-1287 (2002).

Channeltron

Sodium

Page 25: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides
Page 26: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

0.0 0.5 1.0 1.5 2.0

100

101

102 298 K 203 K

Dec

ay ra

te [a

.u.]

Time [ms]

= 0.2 ms

Electron autodetachment from the AMP dianion

Liu et al., J. Chem. Phys., issued for Sept. 1 (2004).

Page 27: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

1 mMicro-channel platedetector

Accelerator with electrospray ion source

Magnet

Ion bunch

Injection

Channeltron

Long-lived component ?

Dump of a remaining beam in the micro-channel plate detector after 34 ms of storage time.

Sodium

Page 28: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

34.00 34.05 34.10 34.150

30

60

90

Cou

nts

Time [ms]

40 s

Dump of beam in the detector after 34 ms of storage time

AMP2

(m/q 172.5)

13C-AMP2

(m/q 173)

Page 29: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

CONCLUSIONS

• Electron transfer to nucleotide anions occurs in

collisions with sodium vapour.

• Electron attachment leads to dehydrogenation of

the nucleobase nitrogens.

• The dehydrogenated dianion is longlived.

Other fragmentation channels than H-loss upon electron attachment ?

Page 30: Dehydrogenation of nucleobases upon electron attachment to isolated nucleotides

ACKNOWLEDGEMENTS

University of Aarhus:

Preben Hvelplund Jens Ulrik Andersen

Shigeo Tomita Bo Liu

Jimmy Rangama

Leopold-Franzens Universität Innsbruck:

Paul Scheier Gabriel Hasan

FUNDING

The Danish Natural Science Research Council

Aarhus Center for Atomic Physics (ACAP)