Author

Matthew G. Alteen

Structural Genomics ConsortiumORCID 0000-0002-9639-7668Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

A.M. EdwardsiD· 2 shared Brandon A. Keith· 2 shared Derek J. WilsoniD· 2 shared Esther WolfiD· 2 shared Hiroaki SugaiD· 2 shared Rachel J. HardingiD· 2 shared Rebeka Cataldo de Oliveira FantiiD· 2 shared Renu ChandrasekaraniD· 2 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersMolecular Biology

A.M. EdwardsORCID

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2 papers

Recent·Most cited

Molecular BiologybioRxivPreprintJun 2, 2026

Macrocyclic Peptide Tools for Huntingtin-bound HAP40

Esther Wolf, Rebeka Cataldo de Oliveira Fanti, Tatsuya Ikenoue…·Rachel J. Harding

The paper develops macrocyclic peptides that target HAP40, enabling the study of HTT-HAP40 interactions and their role in Huntington's disease.

DOI 10.64898/2026.06.02.729325

humanproteomics

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BiochemistrybioRxivPreprintAug 6, 2025

High-Affinity, Structure-Validated and Selective Macrocyclic Peptide Tools for Chemical Biology Studies of Huntingtin

Esther Wolf, Rebeka Cataldo de Oliveira Fanti, Tatsuya Ikenoue…·Rachel Harding

This paper identifies and characterizes high-affinity, selective macrocyclic peptide ligands for Huntingtin, enabling structural and functional studies of HTT and its complex with HAP40.

1 citation

humanproteomics

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