Neukam, M. ; Sala, P. ; Brunner, A.D.* ; Ganß, K. ; Palladini, A. ; Grzybek, M. ; Topcheva, O. ; Vasiljevic, J. ; Broichhagen, J.* ; Johnsson, K.* ; Kurth, T.* ; Mann, M.* ; Coskun, Ü. ; Solimena, M.
     
 
    
        
Purification of time-resolved insulin granules reveals proteomic and lipidomic changes during granule aging.
    
    
        
    
    
        
        Cell Rep. 43:113836 (2024)
    
    
    
		
		
			
				Endocrine cells employ regulated exocytosis of secretory granules to secrete hormones and neurotransmitters. Secretory granule exocytosis depends on spatiotemporal variables such as proximity to the plasma membrane and age, with newly generated granules being preferentially released. Despite recent advances, we lack a comprehensive view of the molecular composition of insulin granules and associated changes over their lifetime. Here, we report a strategy for the purification of insulin secretory granules of distinct age from insulinoma INS-1 cells. Tagging the granule-resident protein phogrin with a cleavable CLIP tag, we obtain intact fractions of age-distinct granules for proteomic and lipidomic analyses. We find that the lipid composition changes over time, along with the physical properties of the membrane, and that kinesin-1 heavy chain (KIF5b) as well as Ras-related protein 3a (RAB3a) associate preferentially with younger granules. Further, we identify the Rho GTPase-activating protein (ARHGAP1) as a cytosolic factor associated with insulin granules.
			
			
				
			
		 
		
			
				
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
    
        Typ der Hochschulschrift
        
    
 
    
        Herausgeber
        
    
    
        Schlagwörter
        Arhgap1 ; Clip Tag ; Cp: Cell Biology ; Cp: Metabolism ; Kif5b ; Rab3a ; Snap Tag ; Granule Aging ; Insulin Granule ; Lipidomics ; Organelle Purification ; Proteomics; Secretory Granules; Preferential Release; Phosphatidic-acid; Beta-cell; C-laurdan; Protein; Glucose; Vesicles; Cholesterol; Trafficking
    
 
    
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        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2024
    
 
    
        Prepublished im Jahr 
        0
    
 
    
        HGF-Berichtsjahr
        2024
    
 
    
    
        ISSN (print) / ISBN
        2211-1247
    
 
    
        e-ISSN
        2211-1247
    
 
    
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	    Band: 43,  
	    Heft: 3,  
	    Seiten: ,  
	    Artikelnummer: 113836 
	    Supplement: ,  
	
    
 
  
        
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            Verlag
            Cell Press
        
 
        
            Verlagsort
            50 Hampshire St, Floor 5, Cambridge, Ma 02139 Usa
        
 
	
        
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        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Pancreatic Islet Research (IPI)
    
 
    
        POF Topic(s)
        90000 - German Center for Diabetes Research
    
 
    
        Forschungsfeld(er)
        Helmholtz Diabetes Center
    
 
    
        PSP-Element(e)
        G-502600-001
G-502600-002
G-502600-013
    
 
    
        Förderungen
        German Center for Diabetes Research (DZD e.V.) - German Ministry for Education and Research
EFRE (European Fund for Regional Development)
Leona M. and Harry B. Helmsley Charitable Trust
JDRF International
Swiss State Secretariat for Education, Research, and Innovation
European Federation of Pharmacological Industries and Associations (EFPIA)
European Union's Framework Program Horizon 2020
Innovative Medicines Initiative 2 Joint Undertaking
German-Israeli Foundation for Scientific Research and Development (GIF)
Dresden International Graduate School for Biomedicine and Bioengineering (DIGS-BB)
    
 
    
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        Erfassungsdatum
        2024-04-29