SharedProteomics interviews Jenny Brodbelt

SharedProteomics talks with University of Texas–Austin's Jenny Brodbelt about the future of mass spectrometry, the ever-growing ASMS conference, and her favorite Austin eatery.

Click here to read the full interview.

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Proteomics Journals

Journal of Proteome Research

Developmental Changes for the Hemolymph Metabolome of Silkworm (Bombyx mori L.)

PGTools: A Software Suite for Proteogenomic Data Analysis and Visualization

Comparison of Two Different Astragali Radix by a 1H NMR-Based Metabolomic Approach

Online Matrix Removal Platform for Coupling Gel-Based Separations to Whole Protein Electrospray Ionization Mass Spectrometry

Quantification of the Host Response Proteome after Herpes Simplex Virus Type 1 Infection

Molecular & Cellular Proteomics

A double-barrel LC-MS/MS system to quantify 96 interactomes per day [Technology]

GAG-ID: Heparan Sulfate and Heparin Glycosaminoglycan High-Throughput Identification Software [Research]

Glycomic analysis of life stages of the human parasite Schistosoma mansoni reveals developmental expression profiles of functional and antigenic glycan motifs. [Research]

Quantitative proteomics of human NPC1I1061T mutant fibroblasts provides insights into the pathogenesis of Niemann-Pick Type C disease [Research]

Simultaneous enrichment of plasma soluble and extracellular vesicular glycoproteins using prolonged ultracentrifugation-ERLIC approach [Technology]

Proteomics

Proteomic analysis of fetal programming-related obesity markers

N-terminal acetylome analysis reveals the specificity of Naa50 (Nat5) and suggests a kinetic competition between N-terminal acetyltransferases and methionine aminopeptidases

Extensive differential protein phosphorylation as intraerythrocytic Plasmodium falciparum schizonts develop into extracellular invasive merozoites

Comprehensive mapping of O-glycosylation in flagellin from Campylobacter jejuni 11168: A multi-enzyme differential ion mobility mass spectrometry approach

A Uniform Field Ion Mobility Study of Melittin and Implications of Low-Field Mobility for Resolving Fine Cross-Sectional Detail in Peptide and Protein Experiments

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