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7AXQ

Structure of the cryo-trapped WDR5:CS-VIP8 cocrystal after illumination at 405 nm and 180 K

Summary for 7AXQ
Entry DOI10.2210/pdb7axq/pdb
Related7AXP
DescriptorWD repeat-containing protein 5, CS-VIP8 (3 entities in total)
Functional Keywordswdr5, cyclic strained visible-light photoswitches, mll1 complex disruption, inhibition of hematopoiesis, transferase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight37579.40
Authors
Werel, L.,Essen, L.-O. (deposition date: 2020-11-10, release date: 2021-12-15, Last modification date: 2024-07-10)
Primary citationAlbert, L.,Nagpal, J.,Steinchen, W.,Zhang, L.,Werel, L.,Djokovic, N.,Ruzic, D.,Hoffarth, M.,Xu, J.,Kaspareit, J.,Abendroth, F.,Royant, A.,Bange, G.,Nikolic, K.,Ryu, S.,Dou, Y.,Essen, L.O.,Vazquez, O.
Bistable Photoswitch Allows in Vivo Control of Hematopoiesis.
Acs Cent.Sci., 8:57-66, 2022
Cited by
PubMed Abstract: Optical control has enabled functional modulation in cell culture with unparalleled spatiotemporal resolution. However, current tools for in vivo manipulation are scarce. Here, we design and implement a genuine optochemical probe capable of achieving hematopoietic control in zebrafish. Our photopharmacological approach first developed conformationally strained visible light photoswitches (CS-VIPs) as inhibitors of the histone methyltransferase MLL1 (KMT2A). In blood homeostasis MLL1 plays a crucial yet controversial role. optimally fulfils the requirements of a true bistable functional system in vivo under visible-light irradiation, and with unprecedented stability. These properties are exemplified via hematopoiesis photoinhibition with a single isomer in zebrafish. The present interdisciplinary study uncovers the mechanism of action of CS-VIPs. Upon WDR5 binding, causes MLL1 release with concomitant allosteric rearrangements in the WDR5/RbBP5 interface. Since our tool provides on-demand reversible control without genetic intervention or continuous irradiation, it will foster hematopathology and epigenetic investigations. Furthermore, our workflow will enable exquisite photocontrol over other targets inhibited by macrocycles.
PubMed: 35106373
DOI: 10.1021/acscentsci.1c00434
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.562 Å)
Structure validation

227111

數據於2024-11-06公開中

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