A new approach to protein sequencing is described. It consists of two
steps: (i) ladder-generating chemistry, the controlled generation from
a polypeptide chain by wet chemistry of a family of sequence-defining
peptide fragments, each differing from the next by one amino acid; an
d (ii) data readout, a one-step readout of the resulting protein seque
ncing ladder by matrix-assisted laser-desorption mass spectrometry. Ea
ch amino acid was identified from the mass difference between successi
ve peaks, and the position in the data set defined the sequence of the
original peptide chain. This method was used to directly locate a pho
sphoserine residue in a phosphopeptide. The protein ladder sequencing
method lends itself to very high sample throughput at very low per cyc
le cost.