Published September 25, 2024 | Version v1
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Structural insights into translocation and tailored synthesis of hyaluronan

Description

Hyaluronan (HA) is an essential component of the vertebrate extracellular matrix. It is a heteropolysaccharide of N-acetylglucosamine (GlcNAc) and glucuronic acid (GlcA) reaching several megadaltons in healthy tissues. HA is synthesized and translocated in a coupled reaction by HA synthase (HAS). Here, structural snapshots of HAS provide insights into HA biosynthesis, from substrate recognition to HA elongation and translocation. We monitor the extension of a GlcNAc primer with GlcA, reveal the coordination of the uridine diphosphate product by a conserved gating loop and capture the opening of a translocation channel to coordinate a translocating HA polymer. Furthermore, we identify channel-lining residues that modulate HA product lengths. Integrating structural and biochemical analyses suggests an avenue for polysaccharide engineering based on finely tuned enzymatic activity and HA coordination.

Data availability

Coordinates and EM maps were deposited to the PDB and EM Data Bank under accession codes 8SMM/EMD-40591, 8SMN/EMD-40594, 8SMP/EMD-40598, 8SND/EMD-40623, 8SNC/EMD-40622 and 8SNE/EMD-40624 for XlHAS1 apo, XlHAS1 HA-bound, XlHAS1 UDP-bound, CvHAS GlcNAc and UDP-GlcA-bound, CvHAS GlcA-extended GlcNAc-bound and CvHAS GlcA-extended GlcNAc and UDP-bound, respectively. Source data are provided with this paper.

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Additional details

Identifiers

DOI
10.1038/s41594-024-01389-1
Other
oai:uchicago.tind.io:13592

Funding

National Institutes of Health
R35GM144130
National Institutes of Health
R01GM117372
Boehringer Ingelheim Fonds
Fellowship

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Biochemistry and Molecular Biology