STED imaging of endogenously tagged ARF GTPases reveals their distinct nanoscale localizations.

ADP-ribosylation factor (ARF) GTPases are major regulators of cellular membrane homeostasis. High sequence similarity and multiple, possibly redundant functions of the five human ARFs make investigating their function a challenging task. To shed light on the roles of the different Golgi-localized ARF members in membrane trafficking, we generated CRISPR-Cas9 knockins (KIs) of type I (ARF1 and ARF3) and type II ARFs (ARF4 and ARF5) and mapped their nanoscale localization with stimulated emission depletion (STED) super-resolution microscopy. We find ARF1, ARF4, and ARF5 on segregated nanodomains on the cis-Golgi and ER-Golgi intermediate compartments (ERGIC), revealing distinct roles in COPI recruitment on early secretory membranes. Interestingly, ARF4 and ARF5 define Golgi-tethered ERGIC elements decorated by COPI and devoid of ARF1. Differential localization of ARF1 and ARF4 on peripheral ERGICs suggests the presence of functionally different classes of intermediate compartments that could regulate bi-directional transport between the ER and the Golgi. Furthermore, ARF1 and ARF3 localize to segregated nanodomains on the trans-Golgi network (TGN) and are found on TGN-derived post-Golgi tubules, strengthening the idea of distinct roles in post-Golgi sorting. This work provides the first map of the nanoscale organization of human ARF GTPases on cellular membranes and sets the stage to dissect their numerous cellular roles.

[1]  C. Freund,et al.  When less is more - Endogenous tagging with TurboID increases the sensitivity of proximity labelling-based experiments , 2021 .

[2]  Francesca Bottanelli,et al.  ARF GTPases and Their Ubiquitous Role in Intracellular Trafficking Beyond the Golgi , 2021, Frontiers in Cell and Developmental Biology.

[3]  J. Lippincott-Schwartz,et al.  A General Method to Improve Fluorophores Using Deuterated Auxochromes , 2021, JACS Au.

[4]  M. Spiess,et al.  Shared and specific functions of Arfs 1–5 at the Golgi revealed by systematic knockouts , 2021, bioRxiv.

[5]  J. Lippincott-Schwartz,et al.  ER-to-Golgi protein delivery through an interwoven, tubular network extending from ER , 2021, Cell.

[6]  Henriette Aksnes,et al.  Efficient and crucial quality control of HAP1 cell ploidy status , 2020, Biology Open.

[7]  Francesca Bottanelli,et al.  Appreciating the small things in life: STED microscopy in living cells , 2020, Journal of Physics D: Applied Physics.

[8]  J. Lippincott-Schwartz,et al.  A general method to optimize and functionalize red-shifted rhodamine dyes , 2020, Nature Methods.

[9]  G. Jürgens,et al.  Coordinated Activation of ARF1 GTPases by ARF-GEF GNOM Dimers Is Essential for Vesicle Trafficking in Arabidopsis , 2020, Plant Cell.

[10]  D. Stalder,et al.  Direct trafficking pathways from the Golgi apparatus to the plasma membrane , 2020, Seminars in Cell & Developmental Biology.

[11]  F. Perez,et al.  Distinct anterograde trafficking pathways of BACE1 and amyloid precursor protein from the TGN and the regulation of amyloid-β production , 2019, Molecular biology of the cell.

[12]  Samuel J. Lord,et al.  If your P value looks too good to be true, it probably is: Communicating reproducibility and variability in cell biology , 2019, 1911.03509.

[13]  R. Jungmann,et al.  The ALFA-tag is a highly versatile tool for nanobody-based bioscience applications , 2019, Nature Communications.

[14]  Anthony X. Ayala,et al.  Rational Design of Fluorogenic and Spontaneously Blinking Labels for Super-Resolution Imaging , 2019, ACS central science.

[15]  J. Cherfils,et al.  ARF GTPases and their GEFs and GAPs: concepts and challenges , 2019, Molecular biology of the cell.

[16]  B. Schwappach,et al.  Dissection of GTPase-activating proteins reveals functional asymmetry in the COPI coat of budding yeast , 2019, Journal of Cell Science.

[17]  F. Wieland,et al.  Proteomic Profiling of Mammalian COPII and COPI Vesicles. , 2019, Cell reports.

[18]  Lei Lu,et al.  The spatial separation of processing and transport functions to the interior and periphery of the Golgi stack , 2018, eLife.

[19]  J. Rothman,et al.  A novel physiological role for ARF1 in the formation of bidirectional tubules from the Golgi , 2017, Molecular biology of the cell.

[20]  Philipp J. Keller,et al.  A general method to fine-tune fluorophores for live-cell and in vivo imaging , 2017, Nature Methods.

[21]  T. Cech,et al.  Live Cell Imaging Reveals the Dynamics of Telomerase Recruitment to Telomeres , 2016, Cell.

[22]  Edward S. Allgeyer,et al.  Two-colour live-cell nanoscale imaging of intracellular targets , 2016, Nature Communications.

[23]  A. VanDongen,et al.  A novel imaging method for quantitative Golgi localization reveals differential intra-Golgi trafficking of secretory cargoes , 2016, Molecular biology of the cell.

[24]  Doris Chen,et al.  Megabase-scale deletion using CRISPR/Cas9 to generate a fully haploid human cell line , 2014, Genome research.

[25]  C. L. Jackson,et al.  Arfs at a Glance , 2014, Journal of Cell Science.

[26]  P. McPherson,et al.  Scyl1 scaffolds class II Arfs to specific subcomplexes of coatomer through the &ggr;-COP appendage domain , 2014, Journal of Cell Science.

[27]  Robert V Farese,et al.  Arf1/COPI machinery acts directly on lipid droplets and enables their connection to the ER for protein targeting , 2013, eLife.

[28]  David A. Scott,et al.  Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity , 2013, Cell.

[29]  Hye-Won Shin,et al.  ARF1 and ARF4 regulate recycling endosomal morphology and retrograde transport from endosomes to the Golgi apparatus , 2013, Molecular biology of the cell.

[30]  R. Beck,et al.  Scission of COPI and COPII Vesicles Is Independent of GTP Hydrolysis , 2013, Traffic.

[31]  J. Klumperman,et al.  The Sec7 Guanine Nucleotide Exchange Factor GBF1 Regulates Membrane Recruitment of BIG1 and BIG2 Guanine Nucleotide Exchange Factors to the Trans-Golgi Network (TGN)* , 2013, The Journal of Biological Chemistry.

[32]  Le Cong,et al.  Multiplex Genome Engineering Using CRISPR/Cas Systems , 2013, Science.

[33]  Hye-Won Shin,et al.  ARF1 and ARF3 are required for the integrity of recycling endosomes and the recycling pathway. , 2012, Cell structure and function.

[34]  J. Briggs,et al.  Coatomer and dimeric ADP ribosylation factor 1 promote distinct steps in membrane scission , 2011, The Journal of cell biology.

[35]  R. Kahn,et al.  Several ADP-ribosylation Factor (Arf) Isoforms Support COPI Vesicle Formation* , 2011, The Journal of Biological Chemistry.

[36]  R. Kahn,et al.  ADP Ribosylation Factors 1 and 4 and Group VIA Phospholipase A2 Regulate Morphology and Intraorganellar Traffic in the Endoplasmic Reticulum–Golgi Intermediate Compartment , 2010, Molecular biology of the cell.

[37]  Y. Shinoda,et al.  Interaction of Calcium-dependent Activator Protein for Secretion 1 (CAPS1) with the Class II ADP-ribosylation Factor Small GTPases Is Required for Dense-core Vesicle Trafficking in the trans-Golgi Network* , 2010, The Journal of Biological Chemistry.

[38]  J. Dacks,et al.  Arf3 Is Activated Uniquely at the trans-Golgi Network by Brefeldin A-inhibited Guanine Nucleotide Exchange Factors , 2010, Molecular biology of the cell.

[39]  R. Beck,et al.  Differential roles of ArfGAP1, ArfGAP2, and ArfGAP3 in COPI trafficking , 2008, The Journal of cell biology.

[40]  E. Hurt,et al.  Membrane curvature induced by Arf1-GTP is essential for vesicle formation , 2008, Proceedings of the National Academy of Sciences.

[41]  J. Presley,et al.  Characterization of class I and II ADP-ribosylation factors (Arfs) in live cells: GDP-bound class II Arfs associate with the ER-Golgi intermediate compartment independently of GBF1. , 2008, Molecular biology of the cell.

[42]  Ileana Slavin,et al.  Rab1b interacts with GBF1 and modulates both ARF1 dynamics and COPI association. , 2007, Molecular biology of the cell.

[43]  R. Russell,et al.  Differential localization of coatomer complex isoforms within the Golgi apparatus , 2007, Proceedings of the National Academy of Sciences.

[44]  Yawei Li,et al.  Isoform-selective effects of the depletion of ADP-ribosylation factors 1-5 on membrane traffic. , 2005, Molecular biology of the cell.

[45]  J. Hay,et al.  Targeting of Arf-1 to the early Golgi by membrin, an ER-Golgi SNARE , 2005, The Journal of cell biology.

[46]  P. Hargrave,et al.  Rhodopsin C terminus, the site of mutations causing retinal disease, regulates trafficking by binding to ADP-ribosylation factor 4 (ARF4). , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[47]  A. Desai,et al.  A Combined Approach for the Localization and Tandem Affinity Purification of Protein Complexes from Metazoans , 2005, Science's STKE.

[48]  J. Donaldson Multiple Roles for Arf6: Sorting, Structuring, and Signaling at the Plasma Membrane* , 2003, Journal of Biological Chemistry.

[49]  M. Schweikert,et al.  Functional reconstitution of COPI coat assembly and disassembly using chemically defined components , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[50]  J. Helms,et al.  Recruitment to Golgi membranes of ADP‐ribosylation factor 1 is mediated by the cytoplasmic domain of p23 , 2001, The EMBO journal.

[51]  J. Cherfils,et al.  The structural GDP/GTP cycle of human Arf6 , 2001, EMBO reports.

[52]  J. Rothman,et al.  Anterograde flow of cargo across the golgi stack potentially mediated via bidirectional "percolating" COPI vesicles. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[53]  R Pepperkok,et al.  COPI-coated ER-to-Golgi transport complexes segregate from COPII in close proximity to ER exit sites. , 2000, Journal of cell science.

[54]  R. Pepperkok,et al.  KDEL Receptor (Erd2p)-mediated Retrograde Transport of the Cholera Toxin A Subunit from the Golgi Involves COPI, p23, and the COOH Terminus of Erd2p , 1998, The Journal of cell biology.

[55]  J. Goldberg,et al.  Structural Basis for Activation of ARF GTPase Mechanisms of Guanine Nucleotide Exchange and GTP–Myristoyl Switching , 1998, Cell.

[56]  J. Rothman,et al.  Binding of coatomer to Golgi membranes requires ADP-ribosylation factor. , 1993, The Journal of biological chemistry.

[57]  P. Argos,et al.  β-COP, a 110 kd protein associated with non-clathrin-coated vesicles and the golgi complex, shows homology to β-adaptin , 1991, Cell.

[58]  J. Rothman,et al.  A new type of coated vesicular carrier that appears not to contain clathrin: Its possible role in protein transport within the Golgi stack , 1986, Cell.

[59]  Michael D. Abràmoff,et al.  Image processing with ImageJ , 2004 .