---
_id: '12163'
abstract:
- lang: eng
  text: Small GTPases play essential roles in the organization of eukaryotic cells.
    In recent years, it has become clear that their intracellular functions result
    from intricate biochemical networks of the GTPase and their regulators that dynamically
    bind to a membrane surface. Due to the inherent complexities of their interactions,
    however, revealing the underlying mechanisms of action is often difficult to achieve
    from in vivo studies. This review summarizes in vitro reconstitution approaches
    developed to obtain a better mechanistic understanding of how small GTPase activities
    are regulated in space and time.
acknowledgement: The authors acknowledge support from IST Austria and helpful comments
  from the anonymous reviewers that helped to improve this manuscript. We apologize
  to the authors of primary literature and outstanding research not cited here due
  to space restraints.
article_processing_charge: Yes (via OA deal)
article_type: review
author:
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
- first_name: Albert
  full_name: Auer, Albert
  id: 3018E8C2-F248-11E8-B48F-1D18A9856A87
  last_name: Auer
  orcid: 0000-0002-3580-2906
- first_name: Gabriel
  full_name: Brognara, Gabriel
  id: D96FFDA0-A884-11E9-9968-DC26E6697425
  last_name: Brognara
- first_name: Hanifatul R
  full_name: Budiman, Hanifatul R
  id: 55380f95-15b2-11ec-abd3-aff8e230696b
  last_name: Budiman
- first_name: Lukasz M
  full_name: Kowalski, Lukasz M
  id: e3a512e2-4bbe-11eb-a68a-e3857a7844c2
  last_name: Kowalski
- first_name: Ivana
  full_name: Matijevic, Ivana
  id: 83c17ce3-15b2-11ec-abd3-f486545870bd
  last_name: Matijevic
citation:
  ama: Loose M, Auer A, Brognara G, Budiman HR, Kowalski LM, Matijevic I. In vitro
    reconstitution of small GTPase regulation. <i>FEBS Letters</i>. 2023;597(6):762-777.
    doi:<a href="https://doi.org/10.1002/1873-3468.14540">10.1002/1873-3468.14540</a>
  apa: Loose, M., Auer, A., Brognara, G., Budiman, H. R., Kowalski, L. M., &#38; Matijevic,
    I. (2023). In vitro reconstitution of small GTPase regulation. <i>FEBS Letters</i>.
    Wiley. <a href="https://doi.org/10.1002/1873-3468.14540">https://doi.org/10.1002/1873-3468.14540</a>
  chicago: Loose, Martin, Albert Auer, Gabriel Brognara, Hanifatul R Budiman, Lukasz
    M Kowalski, and Ivana Matijevic. “In Vitro Reconstitution of Small GTPase Regulation.”
    <i>FEBS Letters</i>. Wiley, 2023. <a href="https://doi.org/10.1002/1873-3468.14540">https://doi.org/10.1002/1873-3468.14540</a>.
  ieee: M. Loose, A. Auer, G. Brognara, H. R. Budiman, L. M. Kowalski, and I. Matijevic,
    “In vitro reconstitution of small GTPase regulation,” <i>FEBS Letters</i>, vol.
    597, no. 6. Wiley, pp. 762–777, 2023.
  ista: Loose M, Auer A, Brognara G, Budiman HR, Kowalski LM, Matijevic I. 2023. In
    vitro reconstitution of small GTPase regulation. FEBS Letters. 597(6), 762–777.
  mla: Loose, Martin, et al. “In Vitro Reconstitution of Small GTPase Regulation.”
    <i>FEBS Letters</i>, vol. 597, no. 6, Wiley, 2023, pp. 762–77, doi:<a href="https://doi.org/10.1002/1873-3468.14540">10.1002/1873-3468.14540</a>.
  short: M. Loose, A. Auer, G. Brognara, H.R. Budiman, L.M. Kowalski, I. Matijevic,
    FEBS Letters 597 (2023) 762–777.
date_created: 2023-01-12T12:09:58Z
date_published: 2023-03-01T00:00:00Z
date_updated: 2023-08-16T08:32:29Z
day: '01'
ddc:
- '570'
department:
- _id: MaLo
doi: 10.1002/1873-3468.14540
external_id:
  isi:
  - '000891573000001'
  pmid:
  - '36448231'
file:
- access_level: open_access
  checksum: 7492244d3f9c5faa1347ef03f6e5bc84
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T08:31:04Z
  date_updated: 2023-08-16T08:31:04Z
  file_id: '14063'
  file_name: 2023_FEBSLetters_Loose.pdf
  file_size: 3148143
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T08:31:04Z
has_accepted_license: '1'
intvolume: '       597'
isi: 1
issue: '6'
keyword:
- Cell Biology
- Genetics
- Molecular Biology
- Biochemistry
- Structural Biology
- Biophysics
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 762-777
pmid: 1
publication: FEBS Letters
publication_identifier:
  eissn:
  - 1873-3468
  issn:
  - 0014-5793
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: In vitro reconstitution of small GTPase regulation
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 597
year: '2023'
...
---
_id: '8988'
abstract:
- lang: eng
  text: The differentiation of cells depends on a precise control of their internal
    organization, which is the result of a complex dynamic interplay between the cytoskeleton,
    molecular motors, signaling molecules, and membranes. For example, in the developing
    neuron, the protein ADAP1 (ADP-ribosylation factor GTPase-activating protein [ArfGAP]
    with dual pleckstrin homology [PH] domains 1) has been suggested to control dendrite
    branching by regulating the small GTPase ARF6. Together with the motor protein
    KIF13B, ADAP1 is also thought to mediate delivery of the second messenger phosphatidylinositol
    (3,4,5)-trisphosphate (PIP3) to the axon tip, thus contributing to PIP3 polarity.
    However, what defines the function of ADAP1 and how its different roles are coordinated
    are still not clear. Here, we studied ADAP1’s functions using in vitro reconstitutions.
    We found that KIF13B transports ADAP1 along microtubules, but that PIP3 as well
    as PI(3,4)P2 act as stop signals for this transport instead of being transported.
    We also demonstrate that these phosphoinositides activate ADAP1’s enzymatic activity
    to catalyze GTP hydrolysis by ARF6. Together, our results support a model for
    the cellular function of ADAP1, where KIF13B transports ADAP1 until it encounters
    high PIP3/PI(3,4)P2 concentrations in the plasma membrane. Here, ADAP1 disassociates
    from the motor to inactivate ARF6, promoting dendrite branching.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: EM-Fac
acknowledgement: "We thank Urban Bezeljak, Natalia Baranova, Mar Lopez-Pelegrin, Catarina
  Alcarva, and Victoria Faas for sharing reagents and helpful discussions. We thank
  Veronika Szentirmai for help with protein purifications. We thank Carrie Bernecky,
  Sascha Martens, and the M.L. lab for comments on the manuscript. We thank the bioimaging
  facility, the life science facility, and Armel Nicolas from the mass spec facility
  at the Institute of Science and Technology (IST) Austria for technical support.
  C.D. acknowledges funding from the IST fellowship program; this work was supported
  by Human Frontier Science Program Young Investigator Grant\r\nRGY0083/2016. "
article_number: e2010054118
article_processing_charge: No
article_type: original
author:
- first_name: Christian F
  full_name: Düllberg, Christian F
  id: 459064DC-F248-11E8-B48F-1D18A9856A87
  last_name: Düllberg
  orcid: 0000-0001-6335-9748
- first_name: Albert
  full_name: Auer, Albert
  id: 3018E8C2-F248-11E8-B48F-1D18A9856A87
  last_name: Auer
  orcid: 0000-0002-3580-2906
- first_name: Nikola
  full_name: Canigova, Nikola
  id: 3795523E-F248-11E8-B48F-1D18A9856A87
  last_name: Canigova
  orcid: 0000-0002-8518-5926
- first_name: Katrin
  full_name: Loibl, Katrin
  id: 3760F32C-F248-11E8-B48F-1D18A9856A87
  last_name: Loibl
  orcid: 0000-0002-2429-7668
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
citation:
  ama: Düllberg CF, Auer A, Canigova N, Loibl K, Loose M. In vitro reconstitution
    reveals phosphoinositides as cargo-release factors and activators of the ARF6
    GAP ADAP1. <i>PNAS</i>. 2021;118(1). doi:<a href="https://doi.org/10.1073/pnas.2010054118">10.1073/pnas.2010054118</a>
  apa: Düllberg, C. F., Auer, A., Canigova, N., Loibl, K., &#38; Loose, M. (2021).
    In vitro reconstitution reveals phosphoinositides as cargo-release factors and
    activators of the ARF6 GAP ADAP1. <i>PNAS</i>. National Academy of Sciences. <a
    href="https://doi.org/10.1073/pnas.2010054118">https://doi.org/10.1073/pnas.2010054118</a>
  chicago: Düllberg, Christian F, Albert Auer, Nikola Canigova, Katrin Loibl, and
    Martin Loose. “In Vitro Reconstitution Reveals Phosphoinositides as Cargo-Release
    Factors and Activators of the ARF6 GAP ADAP1.” <i>PNAS</i>. National Academy of
    Sciences, 2021. <a href="https://doi.org/10.1073/pnas.2010054118">https://doi.org/10.1073/pnas.2010054118</a>.
  ieee: C. F. Düllberg, A. Auer, N. Canigova, K. Loibl, and M. Loose, “In vitro reconstitution
    reveals phosphoinositides as cargo-release factors and activators of the ARF6
    GAP ADAP1,” <i>PNAS</i>, vol. 118, no. 1. National Academy of Sciences, 2021.
  ista: Düllberg CF, Auer A, Canigova N, Loibl K, Loose M. 2021. In vitro reconstitution
    reveals phosphoinositides as cargo-release factors and activators of the ARF6
    GAP ADAP1. PNAS. 118(1), e2010054118.
  mla: Düllberg, Christian F., et al. “In Vitro Reconstitution Reveals Phosphoinositides
    as Cargo-Release Factors and Activators of the ARF6 GAP ADAP1.” <i>PNAS</i>, vol.
    118, no. 1, e2010054118, National Academy of Sciences, 2021, doi:<a href="https://doi.org/10.1073/pnas.2010054118">10.1073/pnas.2010054118</a>.
  short: C.F. Düllberg, A. Auer, N. Canigova, K. Loibl, M. Loose, PNAS 118 (2021).
date_created: 2021-01-03T23:01:23Z
date_published: 2021-01-05T00:00:00Z
date_updated: 2023-08-04T11:20:46Z
day: '05'
department:
- _id: MaLo
- _id: MiSi
doi: 10.1073/pnas.2010054118
external_id:
  isi:
  - '000607270100018'
  pmid:
  - '33443153'
intvolume: '       118'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.2010054118
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 2599F062-B435-11E9-9278-68D0E5697425
  grant_number: RGY0083/2016
  name: Reconstitution of cell polarity and axis determination in a cell-free system
publication: PNAS
publication_identifier:
  eissn:
  - '10916490'
  issn:
  - '00278424'
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: In vitro reconstitution reveals phosphoinositides as cargo-release factors
  and activators of the ARF6 GAP ADAP1
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 118
year: '2021'
...
