Mass Spectrometry in Proteomics and Pathogen Identification Flashcards

1
Q

uses the known sequences of the entire human genome for determining the role of genetics in certain human diseases

A

Genomics

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2
Q

the investigation of the protein products encoded by these genes

A

Proteomics

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3
Q

often used in the discovery of new biochemical markers

A

“shotgun” approach

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4
Q

can be trypsin digested and separated by HPLC or techniques such as two dimensional electrophoresis can be used to separate proteins into individual spots or bands

A

Proteins

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5
Q

used for the analysis of biomolecules, such as peptides and proteins.

A

MALDI-TOF MS

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6
Q

The solvent is ______ and the plate is introduced into the vacuum system of the MALDI-TOF analyze

A

dried

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7
Q

Ions from the sample are focused into the

A

mass spectrometer

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8
Q

The molecular weight of the proteins acquired by mass spectrum is used to determine the identity of the sample and is helpful in determining posttranslational modifications that may have occurred.

A

MALDI-TOF AND SELDI-TOF MS

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9
Q

A modification of MALDI-TOF MS is SELDI-TOF MS, in which proteins are directly captured on a _____________ _______ without the need of sample preparation

A

chromatographic biochip

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10
Q

MS has primarily been utilized in __________ and ____________ sections for the analysis of small molecules and proteins, high-resolution MS can be used for the identification of pathogens in modern ____________ laboratories.

A

chemistry; toxicology; microbiology

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11
Q

This protein “____________” is composed of mainly ribosomal proteins and can be compared with a digital database of species

A

fingerprint

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12
Q

Because MALDI-TOF MS requires inexpensive reagents and only takes _________ minutes per run, it is significantly cheaper and faster than traditional automated biochemical identification techniques.

A

5 to 10

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13
Q

used to amplify DNA from the unknown pathogen and ESI-TOF MS is used to calculate exact masses of these PCR-generated DNA fragments

A

PCR

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14
Q

The unique purine and pyrimidine nucleotide composition of the PCR-generated fragments can then be compared with a preexisting digital library in order to identify the

A

unknown pathogen

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