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Selective and ATP-Dependent Translocation of Peptides by the MHC-Encoded Transporter

Neefjes, Jacques J., Momburg, Frank, Hämmerling, Günter J.·1993·Science

Abstract

Major histocompatibility complex (MHC) class I molecules present peptides derived from nuclear and cytosolic proteins to CD8 + T cells. These peptides are translocated into the lumen of the endoplasmic reticulum (ER) to associate with class I molecules. Two MHC-encoded putative transporter proteins, TAP1 and TAP2, are required for efficient assembly of class I molecules and presentation of endogenous peptides. Expression of TAP1 and TAP2 in a mutant cell line resulted in the delivery of an 11-amino acid oligomer model peptide to the ER. Peptide translocation depended on the sequence of the peptide, was adenosine triphosphate (ATP)-dependent, required ATP hydrolysis, and was inhibited in a concentration-dependent manner.

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Metadata

Authors
Neefjes, J. J., Momburg, F., & Hämmerling, G. J.
Venue
Science
Published
1993-08-06
Volume
261
Issue
5122
Pages
769-771
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2071692669
Cited by
549
References
0
FWCI
17.36
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Selective and ATP-Dependent Translocation of Peptides by the MHC-Encoded Transporter. https://app.cochat.ai/papers/10.1126/science.8342042
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Neefjes, J. J., Momburg, F., & Hämmerling, G. J. (1993). Selective and ATP-Dependent Translocation of Peptides by the MHC-Encoded Transporter. Science. https://doi.org/10.1126/science.8342042

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.