Nanoscale protein architecture of the kidney glomerular basement membrane
Hani Suleiman,
Lei Zhang,
Robyn Roth,
John E Heuser,
Jeffrey H Miner,
Andrey S Shaw,
Adish Dani
Affiliations
Hani Suleiman
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, United States
Lei Zhang
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, United States
Robyn Roth
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, United States
John E Heuser
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, United States
Jeffrey H Miner
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, United States; Renal Division, Department of Medicine, Washington University School of Medicine, St. Louis, United States
Andrey S Shaw
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, United States; Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, United States
Adish Dani
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, United States; Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, United States
In multicellular organisms, proteins of the extracellular matrix (ECM) play structural and functional roles in essentially all organs, so understanding ECM protein organization in health and disease remains an important goal. Here, we used sub-diffraction resolution stochastic optical reconstruction microscopy (STORM) to resolve the in situ molecular organization of proteins within the kidney glomerular basement membrane (GBM), an essential mediator of glomerular ultrafiltration. Using multichannel STORM and STORM-electron microscopy correlation, we constructed a molecular reference frame that revealed a laminar organization of ECM proteins within the GBM. Separate analyses of domains near the N- and C-termini of agrin, laminin, and collagen IV in mouse and human GBM revealed a highly oriented macromolecular organization. Our analysis also revealed disruptions in this GBM architecture in a mouse model of Alport syndrome. These results provide the first nanoscopic glimpse into the organization of a complex ECM.