5n6w | pdb_00005n6w

Retinoschisin R141H Mutant

Loading... Status: waiting for Mol* initialization Structural highlights 5n6w is a 16 chain structure with sequence from Human. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Gene: RS1, XLRS1 (HUMAN) Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease [XLRS1_HUMAN] X-linked retinoschisis. The disease is caused by mutations affecting the gene represented in this entry. Function [XLRS1_HUMAN] May be active in cell adhesion processes during retinal development. Publication Abstract from PubMed Retinoschisin, an octameric retinal-specific protein, is essential for retinal architecture with mutations causing X-linked retinoschisis (XLRS), a monogenic form of macular degeneration. Most XLRS-associated mutations cause intracellular retention, however a subset are secreted as octamers and the cause of their pathology is ill-defined. Therefore, here we investigated the solution structure of the retinoschisin monomer and the impact of two XLRS-causing mutants using a combinatorial approach of biophysics and cryo-EM. The retinoschisin monomer has an elongated structure which persists in the octameric assembly. Retinoschisin forms a dimer of octamers with each octameric ring adopting a planar propeller structure. Comparison of the octamer with the hexadecamer structure indicated little conformational change in the retinoschisin octamer upon dimerization, suggesting that the octamer provides a stable interface for the construction of the hexadecamer. The H207Q XLRS-associated mutation was found in the interface between octamers and destabilized both monomeric and octameric retinoschisin. Octamer dimerization is consistent with the adhesive function of retinoschisin supporting interactions between retinal cell layers, so disassembly would prevent structural coupling between opposing membranes. In contrast, cryo-EM structural analysis of the R141H mutation at approximately 4.2A resolution was found to only cause a subtle conformational change in the propeller tips, potentially perturbing an interaction site. Together, these findings support distinct mechanisms of pathology for two classes of XLRS-associated mutations in the retinoschisin assembly. Structural analysis of X-linked retinoschisis mutations reveals distinct classes which differentially effect retinoschisin function.,Ramsay EP, Collins RF, Owens TW, Siebert CA, Jones RP, Wang T, Roseman AM, Baldock C Hum Mol Genet. 2016 Oct 23. pii: ddw345. doi: 10.1093/hmg/ddw345. PMID:27798099 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

Proteopedia Page Contributors and Editors (what is this?)

OCA