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. Author manuscript; available in PMC: 2012 Jan 30.
Published in final edited form as: Clin Chim Acta. 2010 Oct 27;412(3-4):277–285. doi: 10.1016/j.cca.2010.10.018

Table 3.

Comparison of modification sites identified in this study with modification sites found in previous work with minimally glycated HSA

HSA Sample Modified Region 1a Modified Region 2b Modified Region 3c Overlapping Residues Modification
HSA-5 520–534 520–525 525–534 K521, K524, & K525 FL-1H2O
HSA-2, HSA-5 414–432 426–442 415–439 K439/R428 FL-1H2O or AFGP
HSA-4, HSA-5 426–442 426–442 415–439 K439 FL, FL-H2O, or Pyr
HSA-2, HSA-4 196–205, 198–209 196–209, 191–205 n/a K199, K205 FL, FL-H2O, or Pyr
HSA-5 281–294 286–294 n/a K286 FL-2H2O or CEL
HSA-2, HSA-4, HSA-5 1–10, 1–12, 5–12 7–17 n/a K12 FL, FL-H2O, or CEL
HSA-2, HSA-4 83–100 n/a 71–84 R81 MG-H1
a

Modified region 1 represents the region of HSA that was found to contain modified sites in this current study. The abbreviations used to represent these modifications are defined in Table 1.

b

Modified region 2 represents the region of HSA that was found in Ref. [29] to be modified to form early and late stage glycation products when using a commercial preparation of minimally-glycated HSA.

c

Modified region 3 represents the region of a commercial preparation of minimally-glycated HSA that was previously found in Ref. [30] to have significant levels of glycation, as measured by using 16O/18O-labeling and mass spectrometry.