Literature DB >> 16413279

In vitro assays of Arf1 interaction with GGA proteins.

Hye-Young Yoon1, Juan S Bonifacino, Paul A Randazzo.   

Abstract

ADP-ribosylation factor 1 (Arf1) is a GTP-binding protein that regulates membrane traffic. This function of Arf1 is, at least in part, mediated by Arf1 x GTP binding to coat proteins such as coatomer, clathrin adaptor protein (AP) complexes 1 and 3, and gamma-adaptin homology-Golgi associated Arf-binding (GGA) proteins. Binding to Arf1 x GTP recruits these coat proteins to membranes, leading to the formation of transport vesicles. Whereas coatomer and the AP complexes are hetero-oligomers, GGAs are single polypeptide chains. Therefore, working with recombinant GGAs is straightforward compared to the other Arf1 effectors. Consequently, the GGAs have been used as a model for studying Arf1 interactions with effectors and as reagents to determine Arf1 x GTP levels in cells. In this chapter, we describe in vitro assays for analysis of GGA interaction with Arf1 x GTP and for determining intracellular Arf1 x GTP levels.

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Year:  2005        PMID: 16413279     DOI: 10.1016/S0076-6879(05)04028-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  16 in total

1.  ArfGAP1 promotes COPI vesicle formation by facilitating coatomer polymerization.

Authors:  Yoko Shiba; Ruibai Luo; Jenny E Hinshaw; Tomasz Szul; Ryo Hayashi; Elizabeth Sztul; Kunio Nagashima; Ulrich Baxa; Paul A Randazzo
Journal:  Cell Logist       Date:  2011-07-01

2.  ARAP2 signals through Arf6 and Rac1 to control focal adhesion morphology.

Authors:  Pei-Wen Chen; Xiaoying Jian; Hye-Young Yoon; Paul A Randazzo
Journal:  J Biol Chem       Date:  2013-01-07       Impact factor: 5.157

3.  The adaptor protein and Arf GTPase-activating protein Cat-1/Git-1 is required for cellular transformation.

Authors:  Sungsoo M Yoo; Marc A Antonyak; Richard A Cerione
Journal:  J Biol Chem       Date:  2012-07-17       Impact factor: 5.157

4.  Modifications to the C-terminus of Arf1 alter cell functions and protein interactions.

Authors:  Xiaoying Jian; Margaret Cavenagh; James M Gruschus; Paul A Randazzo; Richard A Kahn
Journal:  Traffic       Date:  2010-02-27       Impact factor: 6.215

5.  A PH domain in the Arf GTPase-activating protein (GAP) ARAP1 binds phosphatidylinositol 3,4,5-trisphosphate and regulates Arf GAP activity independently of recruitment to the plasma membranes.

Authors:  Fanny Campa; Hye-Young Yoon; Vi Luan Ha; Zsofia Szentpetery; Tamas Balla; Paul A Randazzo
Journal:  J Biol Chem       Date:  2009-08-07       Impact factor: 5.157

6.  Highly conserved motifs within the large Sec7 ARF guanine nucleotide exchange factor GBF1 target it to the Golgi and are critical for GBF1 activity.

Authors:  Cristian A Pocognoni; Ekaterina G Viktorova; John Wright; Justyna M Meissner; Garrett Sager; Eunjoo Lee; George A Belov; Elizabeth Sztul
Journal:  Am J Physiol Cell Physiol       Date:  2018-02-14       Impact factor: 4.249

7.  Inhibition of Cytohesins Protects against Genetic Models of Motor Neuron Disease.

Authors:  Jinbin Zhai; Lei Zhang; Jelena Mojsilovic-Petrovic; Xiaoying Jian; Jeffrey Thomas; Kengo Homma; Anton Schmitz; Michael Famulok; Hidenori Ichijo; Yair Argon; Paul A Randazzo; Robert G Kalb
Journal:  J Neurosci       Date:  2015-06-17       Impact factor: 6.167

8.  Arf GAP2 is positively regulated by coatomer and cargo.

Authors:  Ruibai Luo; Vi Luan Ha; Ryo Hayashi; Paul A Randazzo
Journal:  Cell Signal       Date:  2009-03-16       Impact factor: 4.315

9.  A novel small molecule regulator of guanine nucleotide exchange activity of the ADP-ribosylation factor and golgi membrane trafficking.

Authors:  Heling Pan; Jia Yu; Lihong Zhang; Anne Carpenter; Hong Zhu; Li Li; Dawei Ma; Junying Yuan
Journal:  J Biol Chem       Date:  2008-09-17       Impact factor: 5.157

10.  A role for cargo in Arf-dependent adaptor recruitment.

Authors:  Amanda H Caster; Elizabeth Sztul; Richard A Kahn
Journal:  J Biol Chem       Date:  2013-04-09       Impact factor: 5.157

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