Validation of Shewanella oneidensis MR-1 small proteins by AMT tag-based proteome analysis

被引:42
作者
Romine, MF
Elias, DA
Monroe, ME
Auberry, K
Fang, RH
Fredrickson, JK
Anderson, GA
Smith, RD
Lipton, MS [1 ]
机构
[1] Pacific NW Natl Lab, Environm & Mol Sci Lab, Div Biol Separat & Mass Spectrometry, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, Div Biol Sci, Richland, WA 99352 USA
[3] Pacific NW Natl Lab, Div Sci & Expt Resources, Richland, WA 99352 USA
关键词
D O I
10.1089/omi.2004.8.239
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Using stringent criteria for protein identification by accurate mass and time (AMT) tag mass spectrometric methodology, we detected 36 proteins of 101 amino acids in length, including 10 that were annotated as hypothetical proteins, in 172 global tryptic digests of Shewanella oneidensis MR-1 proteins. Peptides that map to the conserved, but functionally uncharacterized proteins SO4134 and SO2787, were the most frequently detected peptides in these samples, while those that map to hypotheticals SO2669 and SO2063, conserved hypotheticals SO0335 and SO2176, and the SlyX protein (SO1063) were observed at frequencies similar to those from essential small proteins (ribosomal proteins and translation. initiation factor IF-1), suggesting that they may function in similarly important cellular functions. In addition, peptides were detected that map to 30 genes predicted to encode frameshifts, point mutations, or recoding signals. Of these 30 genes, peptides that map to positions beyond internal stop codons were detected in 13 genes (SO0101, SO0419, SO0590, SO0738, SO1113, SO1211, SO3079, SO3130, SO3240, SO4231, SO4328, SO4422, and SO4657). While expression of the full-length formate dehydrogenase encoded by SO0101 can be explained by incorporation of selenocysteine at the internal stop codon, the mechanism of translating downstream sequences in the remaining genes remains unknown.
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页码:239 / 254
页数:16
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