Evidence map›Paper›PMID 24815030›Full record

ArticleStructure (London, England : 1993)2014

Key interactions for clathrin coat stability.

Till Böcking, François Aguet, Iris Rapoport, Manuel Banzhaf, Anan Yu, Jean Christophe Zeeh, Tom Kirchhausen

Open access · bronzeAbstract read
In one paragraph

Article in Structure (London, England : 1993), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Clathrin is an Intrinsic Driver of Membrane Fission.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
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  11. Article
  12. Article
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  14. Review
  15. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Till BöckingDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Centre for Vascular Research, University of New South Wales, Sydney NSW 2052 Australia. Electronic address: till.boecking@unsw.edu.au.
François AguetDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Iris RapoportDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA 02115, USA.
Manuel BanzhafDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA 02115, USA.
Anan YuDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA 02115, USA.
Jean Christophe ZeehDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA 02115, USA.
Tom KirchhausenDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA 02115, USA. Electronic address: kirchhausen@crystal.harvard.edu.
Harvard University · USBoston Children's Hospital · US

Funding

Treatments for Nipah Virus InfectionU54AI057159 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WHELAN, SEAN PJ · 2003 to 2013
$113.7M
STRUCTURAL CHEMISTRY OF CLATHRIN &ASSOCIATED PROTEINSR01GM036548 · NIGMS · IMMUNE DISEASE INSTITUTE, INC. · PI KIRCHHAUSEN, TOMAS · 1986 to 2014
$9.8M
Dynamics of Clathrin Coat Formation in CellsR01GM075252 · NIGMS · IMMUNE DISEASE INSTITUTE, INC. · PI KIRCHHAUSEN, TOMAS · 2005 to 2018
$4.6M
NIAID NIH HHS U54 AI057159NIGMS NIH HHS GM-075252NIGMS NIH HHS GM-36548NIGMS NIH HHS R01 GM075252
6 · The paper itself

Abstract

Clathrin-coated vesicles are major carriers of vesicular traffic in eukaryotic cells. This endocytic pathway relies on cycles of clathrin coat assembly and Hsc70-mediated disassembly. Here we identify histidine residues as major determinants of lattice assembly and stability. They are located at the invariant interface between the proximal and distal segments of clathrin heavy chains, in triskelions centered on two adjacent vertices of the coated-vesicle lattice. Mutation of these histidine residues to glutamine alters the pH dependence of coat stability. We then describe single-particle fluorescence imaging experiments in which we follow the effect of these histidine mutations on susceptibility to Hsc70-dependent uncoating. Coats destabilized by these mutations require fewer Hsc70 molecules to initiate disassembly, as predicted by a model in which Hsc70 traps conformational distortions during the auxilin- and Hsc70:ATP-mediated uncoating reaction.

Indexed as

AnimalsAuxilinsBinding SitesCattleClathrin-Coated VesiclesClathrin Heavy ChainsClathrin Light ChainsHistidineHSC70 Heat-Shock ProteinsHydrogen-Ion ConcentrationModels, MolecularMultiprotein ComplexesMutationProtein StabilityRatsRecombinant ProteinsAuxilinsClathrin Heavy ChainsClathrin Light ChainsHistidineHSC70 Heat-Shock ProteinsMultiprotein ComplexesRecombinant Proteins

Identifiers

PMID24815030
PMCPMC4067485
OpenAlexW2073126846

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.