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1 eptide library screening approaches based on Edman sequencing.
2 ion site-specific manner using FT-ICR-MS and Edman sequencing.
3 e determined by tandem mass spectrometry and Edman sequencing.
4 th subsequent mass spectrometric analysis or Edman sequencing.
5 onstrated by successful manual and automated Edman sequencing.
6  released from the membrane were analyzed by Edman sequencing.
7 action, and identification of the residue by Edman sequencing.
8 er-727 using mass spectrometry and automated Edman sequencing.
9 liquid chromatography (HPLC) and analyzed by Edman sequencing.
10 no-terminal cleavage site was identified via Edman sequencing.
11                                        Using Edman sequencing, 125I-SB206718 was shown to cross-link
12 tographic techniques, mass spectrometry, and Edman sequencing, a new hexapeptide (SSLSKL) from the Me
13 P-like kinase, identified by "mixed-peptide" Edman sequencing after affinity purification, as the pre
14 on can then be used for other analyses, such Edman sequencing, amino acid analysis, or proteolytic di
15 me-of-flight mass spectrometry and automated Edman sequencing analysis unequivocally identified the p
16 ites, as determined by mass spectrometry and Edman sequencing analysis.
17  versatility because it is not detectable by Edman sequencing and because it cannot be labeled with r
18 xylesterase ES-10 (EC 3.1.1.1) by N-terminal Edman sequencing and extensive LC-MS/MS sequence analysi
19                                      Through Edman sequencing and in vitro and in vivo biochemistry,
20 ation were determined using a combination of Edman sequencing and LC-MS.
21                           We used N-terminal Edman sequencing and LC-MS/MS analysis to characterize t
22 tic digestion of the heme-protein adduct and Edman sequencing and mass spectrometric analysis of the
23                                              Edman sequencing and mass spectrometry results indicated
24 he primary structure of rPrP was verified by Edman sequencing and mass spectrometry, and secondary st
25 estion products of DGP were characterized by Edman sequencing and mass spectrometry.
26 affinity chromatography and characterized by Edman sequencing and mass spectrometry.
27 acid sequence of this band was determined by Edman sequencing and mass spectroscopy.
28                                        Using Edman sequencing and mutagenesis, we identified a new an
29 rate analog covalently attached to Glu-68 by Edman sequencing and radioanalysis using C18 reverse pha
30 ith phenylisothiocyanate in combination with Edman sequencing, and matrix-assisted laser desorption m
31             We used peptide mapping by HPLC, Edman sequencing, and matrix-assisted time-of-flight (MA
32 tion ionization time-of-flight analysis, and Edman sequencing, demonstrated that NADH attachment occu
33 nsional gels and subjected to NH(2)-terminal Edman sequencing for identification and determination of
34 pectrometry (nanoESI-QTOF MS) and N-terminal Edman sequencing for verifying connectivities.
35                          Further, N-terminal Edman sequencing identified unique autocleavage sites in
36 cation was obtained by mass spectrometry and Edman sequencing in recombinant mouse PrP secreted from
37 rger proteins, efficient deblocking prior to Edman sequencing is especially important to obtain quali
38 se-3 cleavage site of O-GlcNAcase, mapped by Edman sequencing, is a noncanonical recognition site tha
39 ral rounds of HPLC, and gas-phase and manual Edman sequencing, is very tedious and requires about 10
40                                              Edman sequencing, mass spectrometry, ultraviolet-visible
41            Proteins were identified by using Edman sequencing, matrix-assisted laser desorption ioniz
42 erized using gel electrophoresis, N-terminal Edman sequencing, matrix-assisted laser desorption ioniz
43                                              Edman sequencing of cell-associated Iga determined that
44                                              Edman sequencing of class I peptide pools generates "mot
45 andom doedecamer peptide library screen with Edman sequencing of MMP-20 cleavage products revealed th
46   The O-glycosylation site was determined by Edman sequencing of pronase-digested Ambn, which gave HP
47 alyzed by collision-induced dissociation and Edman sequencing of radiolabeled peptides.
48                                              Edman sequencing of the lectin-positive bands gave the A
49 to identify protein phosphorylation sites by Edman sequencing of unseparated peptides.
50 mass spectrometry (ESI-q-TOF-MS), N-terminal Edman sequencing, peptide mapping, and other techniques.
51 nts, with sample cleanup and preparation for Edman sequencing performed using a commercial cartridge
52                                              Edman sequencing revealed that two of the major caspase-
53 Moreover, using tandem mass spectrometry and Edman sequencing, specific intramolecular sites of inter
54 tion, the PrcB N terminus is unavailable for Edman sequencing, suggesting that it is acylated.
55  determined, by a combination of HPLC/MS and Edman sequencing, the glycosylation sites in the extrace
56                                              Edman sequencing was used to assign structure to subsite
57 grated approach, combining MS and N-terminal Edman sequencing, was capable of assigning the disulfide
58                  Using mass spectrometry and Edman sequencing, we have mapped additional phosphorylat
59 ectrospray ionization mass spectrometry, and Edman sequencing, we identified a single luciferase pept
60                                        Using Edman sequencing, we identified furin-type proteinase cl