The corneal stroma is a highly organised matrix of type I collagen fibrils embedded in proteoglycans. Corneal transparency depends on the precise uniform spacing of collagen fibrils (~60 nm apart), which causes destructive interference of scattered light.
The dominant glycosaminoglycan in the corneal stroma is $\text{keratan sulphate}$, carried by proteoglycans such as lumican and keratocan. Keratan sulphate chains regulate fibril spacing; when these chains are abnormal or absent (e.g., in macular corneal dystrophy due to CHST6 mutations), fibril spacing becomes irregular and the cornea becomes opaque.
Other GAGs compared:
- Hyaluronic acid: vitreous humor, synovial fluid -- not cornea
- Chondroitin sulphate: cartilage, minor corneal component
- Heparan sulphate: basement membranes, liver
\[\boxed{\text{Keratan sulphate}}\]