Crystal structure of pre-activated arrestin p44

  • 첨부된 파일이 없습니다.
  • Hit 149
  • Writer 최고관리자
  • 2017-01-06


[S20 Seminar]
                  ▶Subject: Crystal structure of pre-activated arrestin p44
                  ▶Speaker: Prof. Prof. Yong Ju Kim (Chonbuk National University)


                  ▶Date: 2:00 PM/Sept. 26(Mon.)/2016
                  ▶Place: Auditorium(1F), Postech Biotech Center
                  Arrestins interact with G-protein-coupled receptors (GPCRs) to block interaction with G proteins and initiate G-protein-independent signalling. Arrestins have a bi-lobed structure that is stabilized by a long carboxy-terminal tail (C-tail), and displacement of the C-tail by receptor-attached phosphates activates arrestins for binding active GPCRs. Structures of the inactive state of arrestin are available, but it is not known how C-tail displacement activates arrestin for receptor coupling. Here we present a 3.0 Å crystal structure of the bovine arrestin-1 splice variant p44, in which the activation step is mimicked by C-tail truncation. The structure of this pre-activated arrestin is profoundly different from the basal state and gives insight into the activation mechanism. p44 displays breakage of the central polar core and other interlobe hydrogen-bond networks, leading to a ∼21° rotation of the two lobes as compared to basal arrestin-1. Rearrangements in key receptor-binding loops in the central crest region include the finger loop, loop 139 (refs 8, 10, 11) and the sequence Asp 296-Asn 305 (or gate loop), here identified as controlling the polar core. We verified the role of these conformational alterations in arrestin activation and receptor binding by site-directed fluorescence spectroscopy. The data indicate a mechanism for arrestin activation in which C-tail displacement releases critical central-crest loops from restricted to extended receptor-interacting conformations. In parallel, increased flexibility between the two lobes facilitates a proper fitting of arrestin to the active receptor surface. Our results provide a snapshot of an arrestin ready to bind the active receptor, and give an insight into the role of naturally occurring truncated arrestins in the visual system.

              ▶Inquiry: Prof. Cho, Yunje (279-2288)
                    * This seminar will be given in English.
                please refrain from taking photos during seminars. *