Protein-Protein Interactions in Crystals of the Human Receptor-Type Protein Tyrosine Phosphatase ICA512 Ectodomain Primo, María E. Jakancic, Jean Noguera, Martín E. Risso, Valeria Alejandra Sosa, Laura Sica, Mauricio P. Solimena, Michele Poskus, Edgardo Ermácora, Mario R. ICA512 (or IA-2) is a transmembrane protein-tyrosine phosphatase located in secretory granules of neuroendocrine cells. Initially, it was identified as one of the main antigens of autoimmune diabetes. Later, it was found that during insulin secretion, the cytoplasmic domain of ICA512 is cleaved and relocated to the nucleus, where it stimulates the transcription of the insulin gene. The role of the other parts of the receptor in insulin secretion is yet to be unveiled. The structures of the intracellular pseudocatalytic and mature extracellular domains are known, but the transmembrane domain and several intracellular and extracellular parts of the receptor are poorly characterized. Moreover the overall structure of the receptor remains to be established. We started to address this issue studying by X-ray crystallography the structure of the mature ectodomain of ICA512 (ME ICA512) and variants thereof. The variants and crystallization conditions were chosen with the purpose of exploring putative association interfaces, metal binding sites and all other structural details that might help, in subsequent works, to build a model of the entire receptor. Several structural features were clarified and three main different association modes of ME ICA512 were identified. The results provide essential pieces of information for the design of new experiments aimed to assess the structure in vivo. 2024-01-25T12:27:31Z 2024-01-25T12:27:31Z 2011-09-15 info:eu-repo/semantics/article Primo ME, Jakoncic J, Noguera ME, Risso VA, Sosa L, et al. (2011) Protein-Protein Interactions in Crystals of the Human Receptor-Type Protein Tyrosine Phosphatase ICA512 Ectodomain. PLoS ONE 6(9): e24191. doi:10.1371/journal.pone.0024191 https://hdl.handle.net/10481/87304 10.1371/journal.pone.0024191 eng 6;9 http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess Attribution-NonCommercial-NoDerivatives 4.0 Internacional Plos One . PLoS (Public Library of Science)