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
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2
Q

Electrospray Mechanism (3)

A
  1. 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
  2. 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
  3. 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
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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)
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4
Q

Gas Phase Ion Generation

Ion Evaporation Model

A
  • ejection of low molecular weigh species into the gas phase
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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
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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
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7
Q

Native ESI

A

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