7Z01

Z-SBTubA4 photoswitch bound to tubulin-DARPin D1 complex

7Z01 の概要

• エントリーDOI: 10.2210/pdb7z01/pdb
• 分子名称: Tubulin alpha-1B chain, Tubulin beta-2B chain, Designed Ankyrin Repeat Protein (DARPIN) D1, ... (9 entities in total)
• 機能のキーワード: microtubule dynamics; cytoskeleton; photopharmacology; tubulin polymerisation inhibitor; optical control; colchicine; antimitotic; cell division; cell migration; development; photoswitch, cell cycle
• 由来する生物種: synthetic construct; 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 119678.97

構造登録者

Wranik, M.,Weinert, T.,Standfuss, J.,Steinmetz, M. (登録日: 2022-02-21, 公開日: 2022-03-30, 最終更新日: 2024-01-31)

主引用文献

Gao, L.,Meiring, J.C.M.,Varady, A.,Ruider, I.E.,Heise, C.,Wranik, M.,Velasco, C.D.,Taylor, J.A.,Terni, B.,Weinert, T.,Standfuss, J.,Cabernard, C.C.,Llobet, A.,Steinmetz, M.O.,Bausch, A.R.,Distel, M.,Thorn-Seshold, J.,Akhmanova, A.,Thorn-Seshold, O.
In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M.
J.Am.Chem.Soc., 144:5614-5628, 2022

PubMed Abstract: Photoswitchable reagents are powerful tools for high-precision studies in cell biology. When these reagents are globally administered yet locally photoactivated in two-dimensional (2D) cell cultures, they can exert micron- and millisecond-scale biological control. This gives them great potential for use in biologically more relevant three-dimensional (3D) models and , particularly for studying systems with inherent spatiotemporal complexity, such as the cytoskeleton. However, due to a combination of photoswitch isomerization under typical imaging conditions, metabolic liabilities, and insufficient water solubility at effective concentrations, the potential of photoswitchable reagents addressing cytosolic protein targets remains largely unrealized. Here, we optimized the potency and solubility of metabolically stable, druglike colchicinoid microtubule inhibitors based on the styrylbenzothiazole (SBT) scaffold that are nonresponsive to typical fluorescent protein imaging wavelengths and so enable multichannel imaging studies. We applied these reagents both to 3D organoids and tissue explants and to classic model organisms (zebrafish, clawed frog) in one- and two-protein imaging experiments, in which spatiotemporally localized illuminations allowed them to photocontrol microtubule dynamics, network architecture, and microtubule-dependent processes with cellular precision and second-level resolution. These nanomolar, capable photoswitchable reagents should open up new dimensions for high-precision cytoskeleton research in cargo transport, cell motility, cell division, and development. More broadly, their design can also inspire similarly capable optical reagents for a range of cytosolic protein targets, thus bringing photopharmacology one step closer to general realization.

PubMed: 35290733
DOI: 10.1021/jacs.2c01020

実験手法

X-RAY DIFFRACTION (1.82 Å)