De novo sequencing of peptides using MALDI/TOF-TOF

被引:169
作者
Yergey, AL
Coorssen, JR
Backlund, PS
Blank, PS
Humphrey, GA
Zimmerberg, J
Campbell, JM
Vestal, ML
机构
[1] NICHHD, Lab Cellular & Mol Biophys, NIH, Bethesda, MD 20892 USA
[2] Appl Biosyst Inc, Framingham, MA USA
[3] Univ Calgary, Dept Physiol & Biophys, Neurosci Res Grp, Calgary, AB T2N 1N4, Canada
关键词
D O I
10.1016/S1044-0305(02)00393-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The recently developed MALDI TOF-TOF instrument yields relatively complex but interpretable fragmentation spectra. When coupled with a straightforward sequence extension algorithm, it is possible to develop complete peptide sequences de novo from the spectra. This approach has been applied to a set of peptides derived from typtic digestion of electrophoretically separated sea urchin egg membrane proteins. When directed to proteins that have been described previously, the results were in essential agreement with those obtained by conventional data base searching approaches, with certain important exceptions. The present method detected errors in published sequences and was able to develop sequences from peptides differing in mass by one dalton (Da). These results show both the power of the present approach and the need for using de novo methods more frequently than may be otherwise appreciated.
引用
收藏
页码:784 / 791
页数:8
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