Dissecting the Neuroprotective Interaction Between the BH4 Domain of BCL-w and the IP3 Receptor

Overview

Journal Cell Chem Biol

Publisher Cell Press

Specialty Biochemistry

Date 2024 Jul 27

PMID 39067448

Authors

Sophia X Tang

Christina M Camara

Joy A Franco

Maria F Pazyra-Murphy

Yihang Li

Marina Godes

Benjamin M Moyer

Gregory H Bird

Rosalind A Segal

Loren D Walensky

Affiliations

Soon will be listed here.

Abstract

BCL-w is a BCL-2 family protein that promotes cell survival in tissue- and disease-specific contexts. The canonical anti-apoptotic functionality of BCL-w is mediated by a surface groove that traps the BCL-2 homology 3 (BH3) α-helices of pro-apoptotic members, blocking cell death. A distinct N-terminal portion of BCL-w, termed the BCL-2 homology 4 (BH4) domain, selectively protects axons from paclitaxel-induced degeneration by modulating IP3 receptors, a noncanonical BCL-2 family target. Given the potential of BCL-w BH4 mimetics to prevent or mitigate chemotherapy-induced peripheral neuropathy, we sought to characterize the interaction between BCL-w BH4 and the IP3 receptor, combining "staple" and alanine scanning approaches with molecular dynamics simulations. We generated and identified stapled BCL-w BH4 peptides with optimized IP3 receptor binding and neuroprotective activities. Point mutagenesis further revealed the sequence determinants for BCL-w BH4 specificity, providing a blueprint for therapeutic targeting of IP3 receptors to achieve neuroprotection.

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