Author

Mila Trank-Greene

Oregon Health & Science UniversityORCID 0009-0000-4934-3811Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 2 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:proteomics· 2

Frequent Co-Authors

Aidan AnastasiD· 3 shared Fikadu G. TafesseiD· 3 shared John E. BurkeiD· 3 shared Timothy A. BatesiD· 3 shared Eric BarklisiD· 2 shared J. B. Reyes-WeinsteiniD· 2 shared Matthew AH ParsoniD· 2 shared Sintayehu Kebede GurmessaiD· 2 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersBiochemistry

Aidan AnastasORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

MicrobiologybioRxivPreprintJan 27, 2026

Mapping SARS-CoV-2 Nucleocapsid Function with Nanobodies

Jules B. Weinstein, Timothy A. Bates, Aidan Anastas…·Fikadu Tafesse

This study develops domain-specific nanobodies that inhibit SARS-CoV-2 infection by disrupting N protein phase separation and replication.

1 citation

humanproteomics

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BiochemistryNature ProtocolsPeer-reviewedNov 21, 2024

An effective method of measuring nanobody binding kinetics and competition-based epitope mapping using biolayer interferometry

Timothy A. Bates, Sintayehu Kebede Gurmessa, J. B. Reyes-Weinstein…·Fikadu G. Tafesse

The paper describes a method using biolayer interferometry to measure nanobody binding kinetics and perform competition-based epitope mapping.

67 citationstop 1%

experimental assay

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BiochemistryeLifePeer-reviewedDec 1, 2023

ESAT-6 undergoes self-association at phagosomal pH and an ESAT-6 specific nanobody restricts M. tuberculosis growth in macrophages

Timothy A. Bates, Mila Trank-Greene, Xammy Nguyenla…·Fikadu Tafesse

This study investigates ESAT-6's self-association under acidic conditions and shows an ESAT-6-specific nanobody inhibits M. tuberculosis growth in macrophages.

38 citationstop 2%

humanproteomics

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