Virus infections induce production of interferons that act on infected cells to enhance their recognition by CD8 cytotoxic T cells. To counter these mechanisms, viruses often encode proteins that interfere with antigen processing and presentation. In an experiment, cells infected with Virus X are treated with interferon and compared with uninfected cells treated with interferon. Proteasomes are isolated from the two cell populations and their enzymatic activities are compared. The data in figure below show the amino acid preferences for cleavage of peptides by the two samples of proteasomes. Based on these data, Virus X most likely encodes a protein that interferes with: The expression of MHC class I on the surface of the infected cell The rate at which peptides are produced from intact proteins in the infected cell The transport of peptides from the cytosol to the endoplasmic reticulum in the infected cell The replacement of constitutive proteasome subunits with immunoproteasome subunits in the infected cell The development of CD8 T cells in the thymus by inhibiting the thymoproteasome
Virus infections induce production of interferons that act on infected cells to enhance their recognition by CD8 cytotoxic T cells. To counter these mechanisms, viruses often encode proteins that interfere with antigen processing and presentation. In an experiment, cells infected with Virus X are treated with interferon and compared with uninfected cells treated with interferon. Proteasomes are isolated from the two cell populations and their enzymatic activities are compared. The data in figure below show the amino acid preferences for cleavage of peptides by the two samples of proteasomes. Based on these data, Virus X most likely encodes a protein that interferes with: The expression of MHC class I on the surface of the infected cell The rate at which peptides are produced from intact proteins in the infected cell The transport of peptides from the cytosol to the endoplasmic reticulum in the infected cell The replacement of constitutive proteasome subunits with immunoproteasome subunits in the infected cell The development of CD8 T cells in the thymus by inhibiting the thymoproteasome
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
Related questions
Question
Virus infections induce production of interferons that act on infected cells to enhance their recognition by CD8 cytotoxic T cells. To counter these mechanisms, viruses often encode proteins that interfere with antigen processing and presentation. In an experiment, cells infected with Virus X are treated with interferon and compared with uninfected cells treated with interferon. Proteasomes are isolated from the two cell populations and their enzymatic activities are compared. The data in figure below show the amino acid preferences for cleavage of peptides by the two samples of proteasomes.
Based on these data, Virus X most likely encodes a protein that interferes with:
- The expression of MHC class I on the surface of the infected cell
- The rate at which peptides are produced from intact proteins in the infected cell
- The transport of peptides from the cytosol to the endoplasmic reticulum in the infected cell
- The replacement of constitutive proteasome subunits with immunoproteasome subunits in the infected cell
- The development of CD8 T cells in the thymus by inhibiting the thymoproteasome

Transcribed Image Text:The bar graph presented illustrates the percentage of peptides with specific amino acid residues at the first position under two distinct conditions: exposure to Interferon alone (represented by yellow bars) and exposure to both Virus X and Interferon (represented by red bars).
**Graph Details:**
- **Y-Axis:** The y-axis represents the percentage of peptides, ranging from 0% to 25%.
- **X-Axis:** The x-axis lists the amino acid residues at the first position of the peptide, denoted by single-letter codes: L (Leucine), F (Phenylalanine), I (Isoleucine), Y (Tyrosine), D (Aspartic acid), E (Glutamic acid), and Q (Glutamine).
**Interpreting the Data:**
1. **Leucine (L):**
- Interferon: Approximately 23% of peptides.
- Virus X + Interferon: Approximately 10% of peptides.
2. **Phenylalanine (F):**
- Interferon: Approximately 6% of peptides.
- Virus X + Interferon: Approximately 7% of peptides.
3. **Isoleucine (I):**
- Interferon: Approximately 4% of peptides.
- Virus X + Interferon: Approximately 5% of peptides.
4. **Tyrosine (Y):**
- Interferon: Approximately 5% of peptides.
- Virus X + Interferon: Approximately 8% of peptides.
5. **Aspartic Acid (D):**
- Interferon: Approximately 3% of peptides.
- Virus X + Interferon: Approximately 7% of peptides.
6. **Glutamic Acid (E):**
- Interferon: Approximately 4% of peptides.
- Virus X + Interferon: Approximately 6% of peptides.
7. **Glutamine (Q):**
- Interferon: Approximately 2% of peptides.
- Virus X + Interferon: Approximately 4% of peptides.
**Key Observations:**
- The presence of Interferon alone leads to a significantly higher percentage of peptides with Leucine at the first position compared to the co-presence of Virus X and Interferon.
- Under the combined condition of Virus X and Interferon, there is
Expert Solution

This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by step
Solved in 2 steps

Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Recommended textbooks for you

Human Anatomy & Physiology (11th Edition)
Biology
ISBN:
9780134580999
Author:
Elaine N. Marieb, Katja N. Hoehn
Publisher:
PEARSON

Biology 2e
Biology
ISBN:
9781947172517
Author:
Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:
OpenStax

Anatomy & Physiology
Biology
ISBN:
9781259398629
Author:
McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:
Mcgraw Hill Education,

Human Anatomy & Physiology (11th Edition)
Biology
ISBN:
9780134580999
Author:
Elaine N. Marieb, Katja N. Hoehn
Publisher:
PEARSON

Biology 2e
Biology
ISBN:
9781947172517
Author:
Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:
OpenStax

Anatomy & Physiology
Biology
ISBN:
9781259398629
Author:
McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:
Mcgraw Hill Education,

Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:
9780815344322
Author:
Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:
W. W. Norton & Company

Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:
9781260159363
Author:
Martin, Terry R., Prentice-craver, Cynthia
Publisher:
McGraw-Hill Publishing Co.

Inquiry Into Life (16th Edition)
Biology
ISBN:
9781260231700
Author:
Sylvia S. Mader, Michael Windelspecht
Publisher:
McGraw Hill Education