Deciphering the substrate recognition mechanisms of the heparan sulfate 3- <i>O</i> -sulfotransferase-3
Rylee Wander, Andrea M. Kaminski, Yongmei Xu, Vijayakanth Pagadala, J.M. Krahn, Truong Quang Pham, Jian Liu, Lars C. Pedersen
Abstract
-sulfated octasaccharide (8-mer 3). The 8-mer 1 is a known favorable substrate for 3-OST-3, whereas the 8-mer 3 is an unfavorable one. Unlike the 8-mer 1, we discovered that the 8-mer 3 displays two binding orientations to the enzyme: productive binding and non-productive binding. Results from the enzyme activity studies demonstrate that 8-mer 3 can contribute to either substrate or product inhibition, possibly attributed to a non-productive binding mode. Our results suggest that heparan sulfate substrates interact with the 3-OST-3 enzyme in more than one orientation, which may regulate the activity of the enzyme. Our findings also suggest that different binding orientations between polysaccharides and their protein binding partners could influence biological outcomes.