Wyatt Beyers
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Wyatt Beyers has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Santiago M. Di Pietro
Colorado State University 1 Department of Biochemistry and Molecular Biology Fort Collins, CO
2 shared publications Alexander P. Walker
School of Biochemistry, Faculty of Life Sciences, Biomedical Sciences Building, University of Bristol, Bristol, UK
1 shared publicationAnna M. Detry
Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado, USA
1 shared publication- Brett M. Collins
Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia
1 shared publication Cecilia de Heus
Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands
1 shared publication- Chi-Lun Chang
Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, TN, USA
1 shared publication
Latest Publications
- 11 November 2025
- Published by Springer Nature in Nature Chemical Biology
- Vol. 22 (1) , 11-12
Unmasking the FACES of membrane bilayers
- 11 November 2025
- Published by Springer Nature in Nature Chemical Biology
- Vol. 22 (1) , 11-12
Unmasking the FACES of membrane bilayers
- Open Access
- 2 October 2025
- Published by Springer Nature in Nature Communications
- Vol. 16 (1) , 1-21
Identification of a RAB32-LRMDA-Commander membrane trafficking complex reveals the molecular mechanism of human oculocutaneous albinism type 7
The endosomal Commander assembly associates with the sorting nexin-17 (SNX17) cargo adaptor to regulate cell surface recycling of internalised integral proteins including integrins and lipoprotein receptors. Here, we identify leucine rich melanocyte differentiation associated (LRMDA) as a Commander binding protein. We reveal that LRMDA and SNX17 share a common mechanism of Commander association, and that LRMDA simultaneously associates with Commander and active RAB32, establishing distinct RAB32-LRMDA-Commander and SNX17-Commander assemblies. Functional analysis in melanocytes reveals distinct roles for RAB32-LRMDA-Commander and SNX17-Commander in melanosome biogenesis. We reveal how LRMDA mutations, causative for oculocutaneous albinism type 7, a hypopigmentation disorder accompanied by poor visual acuity, uncouple RAB32 and Commander binding thereby establishing the mechanistic basis of this disease. Our discovery of this alternative Commander assembly highlights the plasticity of Commander function in human pigmentation and extends the Commander function beyond the SNX17-mediated regulation of cell surface proteome.
- 2 October 2025
- Published by Springer Nature in Nature Communications
- Vol. 16 (1) , 1-21
Open AccessIdentification of a RAB32-LRMDA-Commander membrane trafficking complex reveals the molecular mechanism of human oculocutaneous albinism type 7
The endosomal Commander assembly associates with the sorting nexin-17 (SNX17) cargo adaptor to regulate cell surface recycling of internalised integral proteins including integrins and lipoprotein receptors. Here, we identify leucine rich melanocyte differentiation associated (LRMDA) as a Commander binding protein. We reveal that LRMDA and SNX17 share a common mechanism of Commander association, and that LRMDA simultaneously associates with Commander and active RAB32, establishing distinct RAB32-LRMDA-Commander and SNX17-Commander assemblies. Functional analysis in melanocytes reveals distinct roles for RAB32-LRMDA-Commander and SNX17-Commander in melanosome biogenesis. We reveal how LRMDA mutations, causative for oculocutaneous albinism type 7, a hypopigmentation disorder accompanied by poor visual acuity, uncouple RAB32 and Commander binding thereby establishing the mechanistic basis of this disease. Our discovery of this alternative Commander assembly highlights the plasticity of Commander function in human pigmentation and extends the Commander function beyond the SNX17-mediated regulation of cell surface proteome.
- Open Access
- 9 November 2022
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 298 (12) , 102669
OCA7 is a melanosome membrane protein that defines pigmentation by regulating early stages of melanosome biogenesis
- 9 November 2022
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 298 (12) , 102669
Open AccessOCA7 is a melanosome membrane protein that defines pigmentation by regulating early stages of melanosome biogenesis