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The required mass of the peptide/protein and the formats allowable depend on several
variables, and these variables will determine the ultimate outcomes. An ideal peptide
(one that is purified and which does not wash off the cartridge matrix) can be sequenced for
20 to 25 cycles at low pmol levels (10 to 15 pmol). However, such samples are scarce. In fact,
buffers, detergents, and other peptides present, as well as the sequence itself, will affect
the results. Copious amounts of Tris and Glycine, salts, as well as detergents, will
also adversely affect the ability to interpret the data or interfere with machine operation.
For PVDF blotted samples, the “rule of thumb” is that a well defined, clearly visible
coomassie stained band blotted to PVDF will generally yield some information. For solution
samples, 50 pmol or so is recommended for strong results; however, samples with 10 to 20 pmol
will produce adequate results.
While these recommendations clearly do not reflect current state-of-the-art analysis,
the PPF finds that “real-world sequencing” is subject to unpredictable variables;
therefore, estimates of producing robust results must be made on the conservative side. Naturally,
it is assumed that the NH2-terminus is not blocked.
Bring your sample to the Purdue Proteomics Facility located in Room B054C in the Hansen Building. Fill
out a Protein Sequence Analysis Request Form, which can be found on the wall outside
the lab. Leave the form and your sample inside the facility with one of the lab technicians.
The Purdue Protein Facility uses the Applied Biosystems Procise 492 Dual Column instrument. This is a completely integrated, computer-controlled device capable of several modes of operation with either blotted or solution (glass fiber matrix) samples. Both gas-phase and pulsed-liquid phase cycles are operational. Data collection is digital, and files can be downloaded to a laser printer for image/data manipulation. There are extra bottle positions for experimental chemistries.