Prince:FASP

Home        Lab Members         Research         Publications         Internal         Mass Spec         Contact        

FASP Protocol

• Template File provides easy calculation of volumes and masses for Solution preparation

FASP Template

Steps

Cell/Tissue Samples:

• Preparing cells/tissue lysate
  • Prepare SDT lysis buffer making sure you have a 1:10 sample:lysis-buffer ratio
  • Bring this amount of lysis buffer to a boil and drop in frozen sample pellet
  • Incubate the lysed cells for 10 min at 95°C
  • Sonicate the lysed cells (Branson SONIFIER 250 for 30 s) (Amplitude 40%) until no longer viscous (DNA broken)
  • Incubate the mixture for 10 min at 95°C
  • Clarify the crude extract by centrifugation at 16,000 x g at room temperature for 10 min.

• Sample processing (for complex sample) times are for 30K filters, when using large filters multiply volume amounts by 50
  • load up to 40 µl (30μL is best) of supernatant with 200µl of UA buffer in 30k filters (Amicon ultra/ Vivacon 500) and vortex it
  • concentrate the solution for 15 min at 14000 × g
  • Add 100µl of UA and centrifuge the filters for 15 min at 14000 × g (twice)
  • Add 100µl of UA-IAA, mix it well and incubate at room temperature for 20 min in dark. Spin out the UA-IAA reagent at 14000 × g for 15 min.
  • Add 100µl of UA centrifuge the filters for 15 min at 14000 × g (twice)
  • Add 100µl of ABC and centrifuge the filters for 20 min at 14000 × g (twice)
  • Add trypsin (proteomic grade) to the sample in the ratio (1:40)
    • mix the required amount of trypsin in 50µl of ABC and add to the filter, vortex it well and pulse the filters to 2000 × g
    • Incubate the samples for 4 h-18 h at 37 °C
  • Transfer the filter units to new collection tubes and centrifuge at 14000 × g
  • wash the filter with 40µl of ABC and centrifuge at 14000 × g
  • Acidify the solution to 1% formic acid

Purified Protein Samples:

• Sample processing (for purified proteins) times are for 30K filters
  • load ~20 µg (have done up to 100) of purified protein in a 1:4 sample:UA buffer ratio in 30k filters and centrifuge for 15 min at 14000 × g
  • Add 100µl of UA-DTT and mix the solution thoroughly centrifuge for 10 min at 14000 × g
  • Add 100µl of UA and centrifuge for 10 min at 14000 × g
  • Add 100µl of UA-IAA, mix it well and incubate at room temperature for 20 min in dark. Spin out the UA-IAA reagent at 14000 × g for 15 min.
  • Add 100µl of UA centrifuge the filters for 15 min at 14000 × g (twice)
  • Add 100µl of ABC and centrifuge the filters for 15 min at 14000 × g (twice)
  • Add trypsin, (0.8 µg proteomic grade) to the sample in the ratio (1:40)
    • mix the required amount of trypsin in 40 µl of ABC and add to the filter, vortex it well and pulse the filters to 2000 × g
    • microwave (inverter based) the sample at 20% power for 1 min and let it cool to room temperature repeat the microwave process again.
  • Transfer the filter units to new collection tubes and centrifuge for 15 min at 14000 × g
  • wash the filter with 40µl of ABC and centrifuge for 15 min at 14000 × g
  • Acidify the solution to 1% formic acid

Buffer Definitions

• UA
  • 8M Urea in 0.1M Tris-HCl @ pH 8.5
• UA/DTT
  • 0.1M DTT in UA buffer
• UA/IAA
  • 50mM IAA in UA buffer
• SDT Lysis Buffer
  • 4% w/v SDS, 0.1M DTT in 0.1M Tris-HCl @ pH 7.6
• ABC
  • 50mM Ammonium Bicarbonate (in MS grade water)

Ordering Information

• Trypsin
  • Sequencing Grade Trypsin from Promega (C/N #V5113) or Trypsin Gold, Mass Spectrometry Grade from Promega (C/N #V5280)
• Filters
  • Sartorius stedim Vivacon 500 Line Vivacon Product Information
    • 100K
    • 50K
    • 30K
    • 10K requires additional 30 minutes/spin
    • 2K we haven't tried yet

Notes

Measuring peptide concentration in eluant

• 1mg/ml solution has 1.1 au at 280nm

Concentration of the peptides can be estimated by UV spectrometer assuming that 0.1% solution of vertebrate proteins has at 280 nm an extinction of 1.1 absorbance units.

Reference

FASP paper (from the supplement of Nature Methods: 6(5) 2009)

Trypsin

Why you do not want to have any residual reducing agent (e.g. DTT) in your digestion buffer:

Trypsin with disulfide bonds

Porcine Trypsin [Green: Backbone, Red: Disulfide bonds]

In Gel FASP Protocol

Also, try our new and improved In-gel FASP method!