A natural tapasin isoform lacking exon 3 modifies peptide loading complex function (Q46799331)

25 December 2017

title

A natural tapasin isoform lacking exon 3 modifies peptide loading complex function (English)

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25 December 2017

11

Stefan Stevanović

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25 December 2017

Anne Halenius

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object named as

Anne Halenius

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25 December 2017

Hartmut Hengel

14

object named as

Hartmut Hengel

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25 December 2017

author name string

Nele Beutler

1

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25 December 2017

Sebastian Hauka

2

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25 December 2017

Alexandra Niepel

3

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25 December 2017

Daniel Johannes Kowalewski

4

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25 December 2017

Julia Uhlmann

5

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25 December 2017

Esther Ghanem

6

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25 December 2017

Steffen Erkelenz

7

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25 December 2017

Constanze Wiek

8

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25 December 2017

Helmut Hanenberg

9

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25 December 2017

Heiner Schaal

10

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25 December 2017

Sebastian Springer

12

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25 December 2017

Frank Momburg

13

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25 December 2017

language of work or name

English

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publication date

10 May 2013

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25 December 2017

European Journal of Immunology

published in

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25 December 2017

volume

43

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25 December 2017

issue

6

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25 December 2017

page(s)

1459-1469

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25 December 2017

Translocation of long peptides by transporters associated with antigen processing (TAP).

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A major role for tapasin as a stabilizer of the TAP peptide transporter and consequences for MHC class I expression

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Soluble tapasin restores MHC class I expression and function in the tapasin-negative cell line .220.

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Tapasin is required for efficient peptide binding to transporter associated with antigen processing

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Recruitment of MHC class I molecules by tapasin into the transporter associated with antigen processing-associated complex is essential for optimal peptide loading

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Multiple residues in the transmembrane helix and connecting peptide of mouse tapasin stabilize the transporter associated with the antigen-processing TAP2 subunit

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A critical role for tapasin in the assembly and function of multimeric MHC class I-TAP complexes

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Direct evidence that the N-terminal extensions of the TAP complex act as autonomous interaction scaffolds for the assembly of the MHC I peptide-loading complex

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Molecular architecture of the TAP-associated MHC class I peptide-loading complex

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Tapasin enhances MHC class I peptide presentation according to peptide half-life

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Optimization of the MHC class I peptide cargo is dependent on tapasin

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Analysis of interactions in a tapasin/class I complex provides a mechanism for peptide selection

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Selective loading of high-affinity peptides onto major histocompatibility complex class I molecules by the tapasin-ERp57 heterodimer

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Tapasin discriminates peptide-human leukocyte antigen-A*02:01 complexes formed with natural ligands

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Human cytomegalovirus disrupts the major histocompatibility complex class I peptide-loading complex and inhibits tapasin gene transcription

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Identification of an alternate splice form of tapasin in human melanoma.

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Splice site strength-dependent activity and genetic buffering by poly-G runs

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Variation in sequence and organization of splicing regulatory elements in vertebrate genes

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Position-dependent splicing activation and repression by SR and hnRNP proteins rely on common mechanisms.

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Frequent gain and loss of intronic splicing regulatory elements during the evolution of vertebrates

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Disulfide bond isomerization and the assembly of MHC class I-peptide complexes

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HLA-B27-restricted antigen presentation in the absence of tapasin reveals polymorphism in mechanisms of HLA class I peptide loading.

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Cytosolic aminopeptidases influence MHC class I-mediated antigen presentation in an allele-dependent manner

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The secondary structure of the human immunodeficiency virus type 1 transcript modulates viral splicing and infectivity

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hnRNP A1 and hnRNP F modulate the alternative splicing of exon 11 of the insulin receptor gene

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Insights into MHC Class I Peptide Loading from the Structure of the Tapasin-ERp57 Thiol Oxidoreductase Heterodimer

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The N-terminal region of tapasin is required to stabilize the MHC class I loading complex

21 January 2018

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The Ig-like domain of tapasin influences intermolecular interactions

21 January 2018

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Productive association between MHC class I and tapasin requires the tapasin transmembrane/cytosolic region and the tapasin C-terminal Ig-like domain

21 January 2018

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Disparate binding of chaperone proteins by HLA-A subtypes

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Transcriptome analysis reveals human cytomegalovirus reprograms monocyte differentiation toward an M1 macrophage

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inferred from DOI database lookup

7 January 2021

based on heuristic

Members of the heterogeneous nuclear ribonucleoprotein H family activate splicing of an HIV-1 splicing substrate by promoting formation of ATP-dependent spliceosomal complexes

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201242725

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/EJI.201242725

1 reference

25 December 2017

PubMed ID

23519916

1 reference

25 December 2017