Six years after coining the term 'mass spectrometric (MS) peptide char
ting' for the component analysis of peptide mixtures in a whole tissue
, body fluid, or an extract thereof, we offer our current perspective
of this field. Matrix-assisted laser desorption/ionization and electro
spray ionization have replaced plasma desorption and fast atom bombard
ment as ionization methods of choice. At the same time, the upper mass
range has been extended to now include most peptides and proteins of
interest to research on cell-cell communication. In addition to qualit
ative aspects, quantitative applications of MS charting have become im
portant. In combination with new database search algorithms, on-line l
iquid chromatography-tandem mass spectrometry promises greater dividen
ds from MS charting than are achievable with molecular mass matching a
lone. We discuss what is and is not yet possible, and consider foresee
able means for overcoming current limitations. Our intent is to encour
age researchers in the biological and medical sciences to take advanta
ge of this powerful methodology in their various fields of endeavor.