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. 2017 May 30;18(6):1160. doi: 10.3390/ijms18061160

Table 2.

Summary of sugar-binding features of the chitin-binding lectins investigated in the present work

Lectin DSA a LEL b PWM c STL d UDA e WGA f
Common features: Binding to chito-oligo
chitotriose-PA (906) N.D. 4.6 μM N.D. N.D. 57 μM 4.7 μM
chitotetraose-PA (907) 43 μM 0.64 μM 53 μM 12 μM 3.8 μM 4.1 μM
Binding to LNH/LNnH
LNnH (type II+ type II; 733) 43 μM 6.7 μM 130 μM 130 μM 29 μM 93 μM
LNH (type I + type II; 734) 19 μM 3.5 μM 93 μM 220 μM 35 μM 110 μM
Unique features:
3 other best PA-oligosaccharides 4.0 μM (323) 2.9 μM (905) 150 μM (004) LacdiNAc-PAA (Glycoconjugate microarray) 3.7 μM (016) 19 μM (053)
4.1 μM (418) 10 μM (903) 300 μM (005) 4.0 μM (014) 19 μM (058)
5.2 μM (420) 39 μM (902) 300 μM (007) 5.5 μM (011) 20 μM (051)

a DSA shows affinity to highly branched N-glycans containing intact type II LacNAc, e.g., 323, 418 and 420; b LEL shows substantial affinity to repeated LacNAc structures, e.g., 902, 903 and 905; c PWM shows relatively weak but significant affinity to a few members of high-mannose-type N-glycans, i.e., 004, 005 and 007.; d STL shows the simplest binding profile among the investigated lectins in FAC, while showing rather selective binding to LacdiNAc-PAA in glycoconjugate microarray; e UDA shows extensive binding to high-mannose-type N-glycans with the structural unit Manα1-3(Manα1-6)Manα1-6Manβ, e.g., 011, 014 and 016; f WGA shows extensive binding to not only GlcNAc-containing glycoconjugates but also those having Neu5Ac clusters. WGA also shows selective binding to hybrid-type N-glycans having bisecting GlcNAc, e.g., 051, 053 and 058. N.D.: Not Detectable.