The type of cells that had the greatest response to an increase in concentration of the engineered RIP. Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

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Answer 1

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Chapter 9, Problem 1DAA

Summary Introduction

To determine: The type of cells that had the greatest response to an increase in concentration of the engineered RIP.

Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

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Answer 2

Question

Chapter 9, Problem 1DAA

Summary Introduction

To determine: The type of cells that had the greatest response to an increase in concentration of the engineered RIP.

Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

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Answer 3

Question

Chapter 9, Problem 1DAA

Summary Introduction

To determine: The type of cells that had the greatest response to an increase in concentration of the engineered RIP.

Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

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Answer 4

Question

Chapter 9, Problem 1DAA

Summary Introduction

To determine: The type of cells that had the greatest response to an increase in concentration of the engineered RIP.

Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

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Answer 5

Chapter 9, Problem 1DAA

Summary Introduction

To determine: The type of cells that had the greatest response to an increase in concentration of the engineered RIP.

Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

Answer 6

Chapter 9, Problem 1DAA

Summary Introduction

To determine: The type of cells that had the greatest response to an increase in concentration of the engineered RIP.

Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

Answer 7

Chapter 9, Problem 1DAA

Summary Introduction

To determine: The type of cells that had the greatest response to an increase in concentration of the engineered RIP.

Introduction: Ribosome-inactivating proteins (RIPs) inactivate the ribosomes and prevent protein synthesis in a cell. It removes adenine base from ribosomal rRNA that forms the part of the binding site for proteins involved in GTP. This results in inability of ribosome to bind to these proteins and protein synthesis stops. The toxic RIPs have a domain that makes them enter into another that interferes with ribosome. They have antiviral and anticancer properties, and are used to design drugs for HIV and cancer.

Answer 8

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Answer 9

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Answer 11

Ch. 9 - A chromosome contains many different genes that...Ch. 9 - A binding .site for RNA polymerase is called a ___...Ch. 9 - An RNA molecule is typically ______; a DNA...Ch. 9 - RNAs form by_____; proteins form by ________. a....Ch. 9 - The main function of a DNA molecule is to ________...Ch. 9 - The main function of an mRNA molecule is to ___ ....Ch. 9 - Prob. 7SQ Ch. 9 - Prob. 1DAA Ch. 9 - Prob. 2DAA Ch. 9 - Prob. 3DAA

Solution Summary: The author explains that RIPs inactivate ribosomes and prevent protein synthesis in a cell. They have antiviral and anticancer properties and are used to design drugs for HIV and cancer.

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