Structural basis for the recognition of Sonic Hedgehog by human Patched1

Author:

Gong Xin1ORCID,Qian Hongwu1ORCID,Cao Pingping1ORCID,Zhao Xin1,Zhou Qiang1ORCID,Lei Jianlin2ORCID,Yan Nieng1ORCID

Affiliation:

1. State Key Laboratory of Membrane Biology, Beijing Advanced Innovation Center for Structural Biology, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences and School of Medicine, Tsinghua University, Beijing 100084, China.

2. Technology Center for Protein Sciences, Ministry of Education Key Laboratory of Protein Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.

Abstract

The first step in Hedgehog signaling The Hedgehog (Hh) signaling pathway is important in embryogenesis; overactivation is associated with cancer. Central to the pathway is the membrane receptor Patched 1 (Ptch1), which indirectly inhibits a G protein–coupled receptor called Smoothened. This inhibition is relieved when Ptch1 binds the secreted protein Hh. Gong et al. report the cryo–electron microscopy structures of human Ptch1 alone and in complex with its Hh ligand at 3.9 and 3.6 Å, respectively. Both structures include two steroid-shaped densities, and mutational analysis indicates that the interaction between Ptch1 and Hh is steroid-dependent. Science , this issue p. eaas8935

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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