7AXP
Structural characterisation of WDR5:CS-VIP8 interaction in cis state 2
Summary for 7AXP
Entry DOI | 10.2210/pdb7axp/pdb |
Descriptor | WD repeat-containing protein 5, CS-VIP8 (3 entities in total) |
Functional Keywords | wdr5, cyclic strained visible-light photoswitches, mll1 complex disruption, inhibition of hematopoiesis, transferase |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 2 |
Total formula weight | 37579.40 |
Authors | Werel, L.,Essen, L.-O. (deposition date: 2020-11-10, release date: 2021-12-15, Last modification date: 2024-07-10) |
Primary citation | Albert, 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: 35106373DOI: 10.1021/acscentsci.1c00434 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.432 Å) |
Structure validation
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