Skip to main content
. 2016 Jul 14;13:87–95. doi: 10.2142/biophysico.13.0_87

Table 1.

Protein–ligand interactions measured by MS under non-denaturing conditions

Proteins (peptides) Ligands KD (μM) References

MS Othersa
FK506 binding protein FK506 (drug) 0.0004 [5]
Globin Heme [6]
Vancomycinb Peptide 1–90 1–170 [13]
OppA Peptide 56–2,900 [22]
Replication terminator protein DNA ≤0.002 0.0005 [23]
Chorismate mutase Inhibitor 1.7 1.0 [24]
RNase A 2′CMPc 2.0 1.0 [25]
hGHbpd Compounde 0.76 0.7 [14]
Beta-peptide Zinc 20 [26]
Antigen binding fragment Hexasaccharide ligand 6.3 5.9 [27]
Norovirus P domain HBGA oligosaccharide 333–2,778 [28]
ABC transporterf Drug and lipid [21]
a

methods except for MS,

b

glycopeptide,

c

cytidine 2′monophosphate,

d

the soluble domain of human growth hormone receptor,

e

neutral nonpolar compounds from the compound collection at Biovitrum AB,

f

ATPbinding cassette transporter P-glycoprotein.