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Yeast Surface Display

Overview of attention for book
Cover of 'Yeast Surface Display'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Protein Engineering and Selection Using Yeast Surface Display.
  3. Altmetric Badge
    Chapter 2 Isolation and Validation of Anti-B7-H4 scFvs from an Ovarian Cancer scFv Yeast-Display Library.
  4. Altmetric Badge
    Chapter 3 Combining Phage and Yeast Cell Surface Antibody Display to Identify Novel Cell Type-Selective Internalizing Human Monoclonal Antibodies.
  5. Altmetric Badge
    Chapter 4 Yeast Display-Based Antibody Affinity Maturation Using Detergent-Solubilized Cell Lysates.
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    Chapter 5 Yeast Endoplasmic Reticulum Sequestration Screening for the Engineering of Proteases from Libraries Expressed in Yeast.
  7. Altmetric Badge
    Chapter 6 T Cell Receptor Engineering and Analysis Using the Yeast Display Platform.
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    Chapter 7 Epitope-Specific Binder Design by Yeast Surface Display.
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    Chapter 8 Applications of Yeast Surface Display for Protein Engineering.
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    Chapter 9 Identification of Novel Protein-Ligand Interactions by Exon Microarray Analysis of Yeast Surface Displayed cDNA Library Selection Outputs.
  11. Altmetric Badge
    Chapter 10 Identification of Posttranslational Modification-Dependent Protein Interactions Using Yeast Surface Displayed Human Proteome Libraries.
  12. Altmetric Badge
    Chapter 11 Utilizing Yeast Surface Human Proteome Display Libraries to Identify Small Molecule-Protein Interactions.
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    Chapter 12 Enzyme Evolution by Yeast Cell Surface Engineering.
  14. Altmetric Badge
    Chapter 13 Electrochemical Glucose Biosensor Based on Glucose Oxidase Displayed on Yeast Surface.
  15. Altmetric Badge
    Chapter 14 Coupling Binding to Catalysis: Using Yeast Cell Surface Display to Select Enzymatic Activities.
  16. Altmetric Badge
    Chapter 15 The Use of Yeast Surface Display in Biofuel Cells.
Attention for Chapter 5: Yeast Endoplasmic Reticulum Sequestration Screening for the Engineering of Proteases from Libraries Expressed in Yeast.
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  • Good Attention Score compared to outputs of the same age and source (69th percentile)

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Chapter title
Yeast Endoplasmic Reticulum Sequestration Screening for the Engineering of Proteases from Libraries Expressed in Yeast.
Chapter number 5
Book title
Yeast Surface Display
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2748-7_5
Pubmed ID
Book ISBNs
978-1-4939-2747-0, 978-1-4939-2748-7
Authors

Yi, Li, Taft, Joseph M, Li, Qing, Gebhard, Mark C, Georgiou, George, Iverson, Brent L, Li Yi, Joseph M. Taft, Qing Li, Mark C. Gebhard, George Georgiou, Brent L. Iverson, Taft, Joseph M., Gebhard, Mark C., Iverson, Brent L.

Abstract

There is significant interest in engineering proteases with desired proteolytic properties. We describe a high-throughput fluorescence-activated cell sorting (FACS) assay for detecting altered proteolytic activity of protease in yeast, at the single cell level. This assay relies on coupling yeast endoplasmic reticulum (ER) retention, yeast surface display, and FACS analysis. The method described here allows facile screening of large libraries, and of either protease or substrate variants, including the screening of protease libraries against substrate libraries. We demonstrate the application of this technique in the screening of libraries of Tobacco Etch Virus protease (TEV-P) for altered proteolytic activities. In addition, the generality of this method is also validated by other proteases such as human granzyme K and the hepatitis C virus protease, and the human Abelson tyrosine kinase.

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 X users 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 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 36%
Student > Ph. D. Student 3 27%
Student > Bachelor 1 9%
Student > Doctoral Student 1 9%
Professor 1 9%
Other 0 0%
Unknown 1 9%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 27%
Chemistry 3 27%
Biochemistry, Genetics and Molecular Biology 2 18%
Immunology and Microbiology 1 9%
Chemical Engineering 1 9%
Other 0 0%
Unknown 1 9%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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 11 June 2015.
All research outputs
#14,786,769
of 23,656,895 outputs
Outputs from Methods in molecular biology
#4,373
of 13,342 outputs
Outputs of similar age
#191,330
of 356,425 outputs
Outputs of similar age from Methods in molecular biology
#280
of 988 outputs
Altmetric has tracked 23,656,895 research outputs across all sources so far. This one is in the 35th percentile – i.e., 35% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,342 research outputs from this source. They receive a mean Attention Score of 3.4. This one has gotten more attention than average, scoring higher than 63% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 356,425 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 43rd percentile – i.e., 43% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 988 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 69% of its contemporaries.