3VHL

Crystal structure of the DHR-2 domain of DOCK8 in complex with Cdc42 (T17N mutant)

Summary for 3VHL

• Entry DOI: 10.2210/pdb3vhl/pdb
• Descriptor: Dedicator of cytokinesis protein 8, Cell division control protein 42 homolog, PHOSPHATE ION, ... (4 entities in total)
• Functional Keywords: signal transduction, guanine nucleotide exchang factor, gtpase, signaling protein
• Biological source: Mus musculus (mouse); More
• Cellular location: Cell membrane; Lipid-anchor; Cytoplasmic side (Potential): P60953
• Total number of polymer chains: 2
• Total formula weight: 55452.26

Authors

Hanawa-Suetsugu, K.,Kukimoto-Niino, M.,Nishizak, T.,Terada, T.,Shirouzu, M.,Fukui, Y.,Yokoyama, S. (deposition date: 2011-08-26, release date: 2012-06-20, Last modification date: 2023-11-08)

Primary citation

Harada, Y.,Tanaka, Y.,Terasawa, M.,Pieczyk, M.,Habiro, K.,Katakai, T.,Hanawa-Suetsugu, K.,Kukimoto-Niino, M.,Nishizaki, T.,Shirouzu, M.,Duan, X.,Uruno, T.,Nishikimi, A.,Sanematsu, F.,Yokoyama, S.,Stein, J.V.,Kinashi, T.,Fukui, Y.
DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses.
Blood, 119:4451-4461, 2012

PubMed Abstract: To migrate efficiently through the interstitium, dendritic cells (DCs) constantly adapt their shape to the given structure of the extracellular matrix and follow the path of least resistance. It is known that this amoeboid migration of DCs requires Cdc42, yet the upstream regulators critical for localization and activation of Cdc42 remain to be determined. Mutations of DOCK8, a member of the atypical guanine nucleotide exchange factor family, causes combined immunodeficiency in humans. In the present study, we show that DOCK8 is a Cdc42-specific guanine nucleotide exchange factor that is critical for interstitial DC migration. By generating the knockout mice, we found that in the absence of DOCK8, DCs failed to accumulate in the lymph node parenchyma for T-cell priming. Although DOCK8-deficient DCs migrated normally on 2-dimensional surfaces, DOCK8 was required for DCs to crawl within 3-dimensional fibrillar networks and to transmigrate through the subcapsular sinus floor. This function of DOCK8 depended on the DHR-2 domain mediating Cdc42 activation. DOCK8 deficiency did not affect global Cdc42 activity. However, Cdc42 activation at the leading edge membrane was impaired in DOCK8-deficient DCs, resulting in a severe defect in amoeboid polarization and migration. Therefore, DOCK8 regulates interstitial DC migration by controlling Cdc42 activity spatially.

PubMed: 22461490
DOI: 10.1182/blood-2012-01-407098

Experimental method

X-RAY DIFFRACTION (2.085 Å)