Electrospray Ionization Flashcards
1
Q
Electrospray Ionization (4)
A
- soft ionization methods
- can be operated in positive or negative modes (i.e. positive mode is for positive gas-phase ions)
- sample can be prepared in an acidic buffer with an organic solvent (denatured ESI) or in an aqueous buffer with a physcial pH and no organic solvent (native ESI)
- sample is pumped through a capillary column at microliters per minute. the capillary is coated with metal and a high voltage (1-5kV) is applied to the end
2
Q
Electrospray Mechanism (3)
A
- Droplet Formation
- electrostatic force in the liquid causes oppositely charged ions to migrate away from one another
- Coulombic repulsion and surface tension cause a “Taylor Cone” at the tip of the capillary
- with increasing electric force due to the applied voltage charged droplets micormeters in size can break away
- when operated in the positive mode oxidation in the solution occurs at the metal contact and reduction at the counterelectrode
- Droplet Shrinkage
- evaporation leads to smaller charged droplets
- charge density of the droplets increases as they shrink leading to the Rayleigh instability limit
- repulsive Coulombic forces exceed surface tension causing fission of droplets into smaller and highly charged offspring droplets
- evaporation leads to smaller charged droplets
- Desorption of Gaseous Ions
- as solvent evapotation and droplet fission is repeated several times a nanometer sized highly charged droplet remains
- depending upon how the ESI was conducted gas phase positive ions are generated by a specific mechanism
3
Q
Initial Droplet Charge
A
- protons are often the main contribututor to net droplet charge
- they can come from acidic buffer and can also be generated at the metal/solution interface inside the capillary (the ESI represents an electrochemical cell)
4
Q
Gas Phase Ion Generation
Ion Evaporation Model
A
- ejection of low molecular weigh species into the gas phase
5
Q
Gas Phase Ion Generation
Charged Residue Model
A
- native ESI technique
- large globular species such as natively folded proteins are released into the gas phase
- proteins are prepared in an aqueous buffer (ammonium acetate or ammonium bicarbonate) with a pH close to 7 (physical pH) with no organics
- important for the analysis of protein-protein interactinoos or protein-small molecular interactions
- it can keep the non-covalent interaction and allows for the topological investigation of intact protein complexes
6
Q
Gas Phase Ion Generation
Chain Ejection Model
A
- disordered, partially hydrophobic, and capable of binding excess charge carriers
- unfolded proteins/peptides
- denatured ESI technique
- proteins are dissolved in acidic buffers with organic solvents
7
Q
Native ESI
A
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