Selective targeting of NaV1.7 via inhibition of the CRMP2-Ubc9 interaction reduces pain in rodents

Author:

Cai Song1ORCID,Moutal Aubin1ORCID,Yu Jie1ORCID,Chew Lindsey A.1ORCID,Isensee Jörg2ORCID,Chawla Reena3,Gomez Kimberly1ORCID,Luo Shizhen1ORCID,Zhou Yuan1ORCID,Chefdeville Aude1ORCID,Madura Cynthia1ORCID,Perez-Miller Samantha14ORCID,Bellampalli Shreya Sai1ORCID,Dorame Angie1,Scott David D.1,François-Moutal Liberty1ORCID,Shan Zhiming1,Woodward Taylor5ORCID,Gokhale Vijay36ORCID,Hohmann Andrea G.5ORCID,Vanderah Todd W.17,Patek Marcel89ORCID,Khanna May1348ORCID,Hucho Tim2ORCID,Khanna Rajesh13478ORCID

Affiliation:

1. Department of Pharmacology, College of Medicine, The University of Arizona, Tucson, AZ 85724, USA.

2. Department of Anesthesiology and Intensive Care Medicine, Translational Pain Research, University Hospital of Cologne, University Cologne, Joseph-Stelzmann-Str 9, Cologne D-50931, Germany.

3. BIO5 Institute, 1657 East Helen Street, Tucson, AZ 85721, USA.

4. Center for Innovation in Brain Sciences, University of Arizona, Tucson, AZ 85721, USA.

5. Department of Psychological and Brain Sciences, Program in Neuroscience and Gill Center for Biomolecular Science, Indiana University, Bloomington, IN 47405-2204, USA.

6. College of Pharmacy, University of Arizona, 1703 East Mabel Street, Tucson, AZ 85721, USA.

7. Comprehensive Pain and Addiction Center, The University of Arizona, Tucson, AZ 85724, USA.

8. Regulonix LLC, 1555 E. Entrada Segunda, Tucson, AZ 85718, USA.

9. Bright Rock Path LLC, Tucson, AZ 85724, USA.

Abstract

Protein-protein interaction inhibitor of the sodium NaV1.7 channel has analgesic effects in preclinical models of pain.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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