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Nanoproteomics

Overview of attention for book
Cover of 'Nanoproteomics'

Table of Contents

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    Book Overview
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    Chapter 1 MALDI-TOF Serum Profiling Using Semiautomated Serum Peptide Capture with Magnetic Reversed Phase (C18) Beads
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    Chapter 2 Nanoproteomics
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    Chapter 3 Protein Identification Using Nano-HPLC-MS: ESI-MS and MALDI-MS Interfaces
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    Chapter 4 Three-Dimensional Peptide Fractionation for Highly Sensitive Nanoscale LC-Based Shotgun Proteomic Analysis of Complex Protein Mixtures
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    Chapter 5 Nanospray Ion Mobility Mass Spectrometry of Selected High Mass Species
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    Chapter 6 Nanoelectrospray-MS n of Native and Permethylated Glycans
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    Chapter 7 N-Linked Global Glycan Profiling by NanoLC Mass Spectrometry
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    Chapter 8 Applications of Nanoscale Liquid Chromatography Coupled to Tandem Mass Spectrometry in Quantitative Studies of Protein Expression, Protein–Protein Interaction, and Protein Phosphorylation
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    Chapter 9 Nano LC–MS/MS: A Robust Setup for Proteomic Analysis
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    Chapter 10 Nanofluidic Devices for Rapid Continuous-Flow Bioseparation
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    Chapter 11 Quantifying Attomole Amounts of Proteins from Complex Samples by Nano-LC and Selected Reaction Monitoring
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    Chapter 12 A Sample Preparation Method for Gold Nanoparticle-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry
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    Chapter 13 Nanostructured TiO 2 Thin Films for Phosphoproteomics Studies with MALDI Mass Spectrometry
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    Chapter 14 Nanofilament Silicon for Matrix-Free Laser Desorption/Ionization Mass Spectrometry
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    Chapter 15 Protein Nanoarrays for High-Resolution Patterning of Bacteria on Gold Surfaces
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    Chapter 16 Engineered Multifunctional Nanotools for Biological Applications
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    Chapter 17 Selective Capture of Phosphopeptides by Zirconium Phosphonate-Magnetic Nanoparticles
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    Chapter 18 Nanowire biosensors for label-free, real-time, ultrasensitive protein detection.
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    Chapter 19 Generation of anti-infectome/anti-proteome nanobodies.
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    Chapter 20 Isolation, Propagation, and Analysis of Biological Nanoparticles.
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    Chapter 21 Functionalized Soluble Nanopolymers for Phosphoproteome Analysis
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    Chapter 22 Elucidating Structural Dynamics of Integral Membrane Proteins on Native Cell Surface by Hydroxyl Radical Footprinting and Nano LC-MS/MS
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    Chapter 23 Application of Electrostatic Repulsion Hydrophilic Interaction Chromatography to the Characterization of Proteome, Glycoproteome, and Phosphoproteome Using Nano LC–MS/MS
Attention for Chapter 20: Isolation, Propagation, and Analysis of Biological Nanoparticles.
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Chapter title
Isolation, Propagation, and Analysis of Biological Nanoparticles.
Chapter number 20
Book title
Nanoproteomics
Published in
Methods in molecular biology, January 2011
DOI 10.1007/978-1-61779-319-6_20
Pubmed ID
Book ISBNs
978-1-61779-318-9, 978-1-61779-319-6
Authors

Michael P. Linnes, Farooq A. Shiekh, Larry W. Hunter, Virginia M. Miller, John C. Lieske, Linnes, Michael P., Shiekh, Farooq A., Hunter, Larry W., Miller, Virginia M., Lieske, John C.

Abstract

Calcifying biologic nanoparticles (NPs) have been implicated as nucleation points for a number of -pathologic events that include vascular calcification and the formation of kidney stones. In order to study these potential relationships, reproducible isolation of well-characterized biologic NPs is a necessity. Our group has isolated and propagated calcifying NPs from several human tissues and renal stones. Specific proteins that could nucleate a calcium phosphate shell under physiologic conditions have been identified as part of their structure, including elongation factor Tu (EF-Tu) and fetuin-A. Visualization, using advanced transmission electron microscopy (TEM), immunofluorescence microscopy, and nuclear and antibody staining in conjunction with flow cytometry, can further elucidate NPs composition and their role in pathology. In order to allow uniform investigation by others, the isolation, culture, and handling procedures for biologic NPs from human calcified vascular tissue and kidney stones are reported in detail.

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The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
France 1 17%
Australia 1 17%
Unknown 4 67%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 1 17%
Professor 1 17%
Student > Ph. D. Student 1 17%
Student > Master 1 17%
Professor > Associate Professor 1 17%
Other 0 0%
Unknown 1 17%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 2 33%
Agricultural and Biological Sciences 2 33%
Medicine and Dentistry 1 17%
Unknown 1 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 03 October 2011.
All research outputs
#18,297,449
of 22,653,392 outputs
Outputs from Methods in molecular biology
#7,801
of 13,011 outputs
Outputs of similar age
#159,894
of 180,249 outputs
Outputs of similar age from Methods in molecular biology
#166
of 229 outputs
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So far Altmetric has tracked 13,011 research outputs from this source. They receive a mean Attention Score of 3.3. This one is in the 24th percentile – i.e., 24% of its peers scored the same or lower than it.
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We're also able to compare this research output to 229 others from the same source and published within six weeks on either side of this one. This one is in the 13th percentile – i.e., 13% of its contemporaries scored the same or lower than it.