Unknown

Dataset Information

0

A combined computational and structural model of the full-length human prolactin receptor.


ABSTRACT: The prolactin receptor is an archetype member of the class I cytokine receptor family, comprising receptors with fundamental functions in biology as well as key drug targets. Structurally, each of these receptors represent an intriguing diversity, providing an exceptionally challenging target for structural biology. Here, we access the molecular architecture of the monomeric human prolactin receptor by combining experimental and computational efforts. We solve the NMR structure of its transmembrane domain in micelles and collect structural data on overlapping fragments of the receptor with small-angle X-ray scattering, native mass spectrometry and NMR spectroscopy. Along with previously published data, these are integrated by molecular modelling to generate a full receptor structure. The result provides the first full view of a class I cytokine receptor, exemplifying the architecture of more than 40 different receptor chains, and reveals that the extracellular domain is merely the tip of a molecular iceberg.

SUBMITTER: Bugge K 

PROVIDER: S-EPMC4869255 | biostudies-literature | 2016 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

A combined computational and structural model of the full-length human prolactin receptor.

Bugge Katrine K   Papaleo Elena E   Haxholm Gitte W GW   Hopper Jonathan T S JT   Robinson Carol V CV   Olsen Johan G JG   Lindorff-Larsen Kresten K   Kragelund Birthe B BB  

Nature communications 20160513


The prolactin receptor is an archetype member of the class I cytokine receptor family, comprising receptors with fundamental functions in biology as well as key drug targets. Structurally, each of these receptors represent an intriguing diversity, providing an exceptionally challenging target for structural biology. Here, we access the molecular architecture of the monomeric human prolactin receptor by combining experimental and computational efforts. We solve the NMR structure of its transmembr  ...[more]

Similar Datasets

| S-EPMC5857566 | biostudies-literature
| S-EPMC5704289 | biostudies-literature
| S-EPMC6921004 | biostudies-literature
| S-EPMC8887629 | biostudies-literature
| S-EPMC7483370 | biostudies-literature
| EMPIAR-10435 | biostudies-other
| EMPIAR-10458 | biostudies-other
| S-EPMC1796749 | biostudies-literature
| S-EPMC7062719 | biostudies-literature
2023-06-26 | PXD037030 | Pride