| Literature DB >> 33839414 |
Jaewon Chang1, Yonugseok Baek2, Injee Lee2, Hiroshi Sekiguchi3, Kouhei Ichiyanagi4, Kazuhiro Mio5, Shunsuke Nozawa6, Ryo Fukaya6, Shin-Ichi Adachi6, Masahiro Kuramochi7, Yuji C Sasaki8.
Abstract
Interleukin 15 receptor (IL-15R) is a transmembrane signalling protein consisting of 3 subsets: α, β (IL-15Rβ), and γ (γc). IL-2 and IL-15 share the signalling domains IL-15Rβ and γc, although they bind to intrinsic α-subsets and non-signalling domains. Additionally, IL-2 and IL-15 play different roles; therefore, there have been many observations of the dynamic behaviours of IL-15R, which are linked to physiological functions. For more practical discrimination between IL-2 and IL-15, a study was designed and carried out in which α-subsets were removed and a cytoplasmic inhibitor was applied to create a simplified environment in which secondary signalling molecules were reduced. We also applied a new measurement method, diffracted X-ray blinking (DXB), to achieve higher accuracy (<0.01 Å). The dynamics of IL-2 binding (confined motion, max range = 0.71 Å) and IL-15 binding (normal motion) in live natural killer cells were different. We also confirmed. that DXB was a suitable method to quantitatively evaluate the transmembrane protein dynamics of inner/outer live cell membranes by labeling the extracellular domain since the measurements were dependent on the cytosolic environment.Entities:
Keywords: Diffracted X-ray blinking; Dynamics in; Ecto-/cytosolic domain; Interleukins with sharing receptor; Intramolecular dynamics; Live human NK cell
Year: 2021 PMID: 33839414 DOI: 10.1016/j.bbrc.2021.03.144
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575