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Updated: Aug 17, 2026

Lipid Droplet Isolation for Quantitative Mass Spectrometry Analysis
Published on: April 17, 2017
Characterization of a noncovalent lipocalin complex by liquid chromatography/electrospray ionization mass
Catalin E Doneanu1, Roland K Strong, William N Howald
1Mass Spectrometry Center, Department of Medicinal Chemistry, University of Washington, Box 357610, Seattle, WA, 98195, USA. doneanu@u.washington.edu
Abstract:
Nanoscale liquid chromatography coupled to electrospray ionization mass spectrometry was used to identify the nature of the ligand that binds noncovalently to siderocalin (lipocalin 2). The folded state siderocalin-ligand complex was separated from free, unfolded siderocalin using reversed phase chromatography, and the molecular weight of the siderocalin ligand was then determined from the deconvoluted molecular weights of the complex and of the free protein. The ligand was identified as dihydroxybenzoyl-serine, a breakdown product of enterobactin, an iron-chelating compound ("siderophore") synthesized in bacteria. These results demonstrate that, in some cases, electrostatic noncovalent protein complexes can survive the denaturing conditions of reversed phase liquid chromatography and the gas phase transfer occurring during electrospray ionization.
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