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Tandem Mass Spectrometry01:21

Tandem Mass Spectrometry

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Tandem mass spectrometry is a technique that uses multiple mass analyzers in series to obtain a higher selectivity and reduce chemical noise during analyte detection. Instruments with multiple analyzers separated by an interaction cell enable secondary fragmentation and selected study of the fragment ions.Secondary fragmentations occur in the interaction cell and can be induced by various factors. Fragmentation induced by collision with inert gases, such as N2, Ar, He, etc., is called...
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MALDI-TOF Mass Spectrometry01:19

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Mass spectrometry is a powerful characterization technique that can identify and separate a wide variety of compounds ranging from chemical to biological entities, based on their mass-to-charge ratio (m/z). The instruments that allow this detection, known as mass spectrometers, have three components: an ion source, a mass analyzer, and a detector. These spectrometers differ based on the nature of their ion source and analyzers.Matrix-assisted laser desorption ionization (MALDI) is a commonly...
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The resolution of a mass spectrometer depends on the efficiency of separating ions with different ion masses. The mass of an atom is approximated to the sum of the masses of protons and neutrons inside, considering the masses of protons and neutrons as equal. However, the masses of the proton (1.6726 × 10−24 g) and neutron (1.6749 × 10−24 g) are not truly equal. There is a minor error in the expression of atomic masses relative to the simplest atom of hydrogen. For...
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Mass Spectrometry: Complex Analysis01:21

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Mass spectrometry is an important technique for the identification of pure compounds. However, it has some limitations for the analysis of complex mixtures, often due to excessive fragmentation making the spectrum too complicated to decipher. Mass spectrometry can be combined with suitable separation methods in sequence, forming hyphenated methods, which are useful in the analysis of complex mixtures.
GC–MS is a powerful hyphenated method commonly used in forensics and environmental...
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Mass Spectrometers01:16

Mass Spectrometers

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This lesson details the instrumentation of a mass spectrometer—a physical instrument to perform mass spectrometry on analyte molecules and record the characteristic mass spectra. This is achieved via three chief functions:
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Peptide Identification Using Tandem Mass Spectrometry01:33

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Tandem mass spectrometry, also known as MS/MS or MS2, is an analytical technique that employs two mass analyzers. Essentially it is a series of mass spectrometers that helps isolate a particular biomolecule and then helps study its chemical properties.
This technique helps gather information regarding the protein from which the peptide was obtained and to study the peptides’ amino acid sequence. Identifying peptides from a complex mixture is an important component of the growing field of...
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Related Experiment Video

Updated: May 4, 2026

Simultaneous Affinity Enrichment of Two Post-Translational Modifications for Quantification and Site Localization
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Simultaneous Affinity Enrichment of Two Post-Translational Modifications for Quantification and Site Localization

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A high dynamic range pulse counting detection system for mass spectrometry.

Bruce A Collings1, Martian D Dima, Gordana Ivosev

  • 1AB Sciex, 71 Four Valley Dr., Concord, Ontario, L4K 4V8, Canada.

Rapid Communications in Mass Spectrometry : RCM
|December 17, 2013
PubMed
Summary
This summary is machine-generated.

A new pulse counting system achieves 2e8 counts per second (cps) on a triple quadrupole mass spectrometer, significantly extending detector dynamic range. This advancement overcomes previous limitations, enabling more sensitive and accurate measurements in mass spectrometry applications.

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Area of Science:

  • Analytical Chemistry
  • Mass Spectrometry Instrumentation

Background:

  • Previous pulse counting systems were limited to approximately 1e7 counts per second (cps).
  • A need exists for detectors with higher dynamic range in mass spectrometry.

Purpose of the Study:

  • To develop and describe a high dynamic range pulse counting system for mass spectrometry.
  • To enhance the upper limit of detection rates for pulse counting systems.

Main Methods:

  • Utilized a high gain transimpedance amplifier with a multi-channel electron multiplier.
  • Employed non-paralyzing detection electronics and a modified dead time correction algorithm.
  • Operated the electron multiplier at a lower bias potential.

Main Results:

  • Achieved a pulse counting capability of up to 2e8 cps on a triple quadrupole mass spectrometer.
  • Demonstrated a linear dynamic range of nearly five orders of magnitude for aprazolam analysis.
  • Extended the detector's linear dynamic range by approximately two orders of magnitude.

Conclusions:

  • A novel high dynamic range pulse counting system capable of operating at 2e8 cps has been successfully developed.
  • This system significantly expands the linear dynamic range of triple quadrupole mass spectrometers.
  • The advancements in detection electronics and dead time correction offer improved performance for high-throughput analyses.