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Chapter 4 - Molecular Cell Biology

from Section 1 - Principles Of Cellular And Molecular Biology

Published online by Cambridge University Press:  04 June 2019

Natalie A Whalley
Affiliation:
PhD, lectures in the Division of Molecular Medicine and Haematology, School of Pathology, University of the Witwatersrand.
Sarah Walters
Affiliation:
BSc (Hons), MSc (Med) (Genetic Counselling), worked as a genetic counsellor in the Division of Human Genetics, University of the Witwatersrand, from 2001 to 2007. In 2007 she became Honorary Treasurer of the Southern African Inherited Disorders Association and began setting up the Birth Defects and Disabilities Foundation (BDDF). She is currently coordinator of the BDDF and programme director of the Medical Genetics Education Programme for registered nurses.
Kate Hammond
Affiliation:
BSc (Hons), MT, PhD, is Professor of Molecular Medicine and Haematology, University of the Witwatersrand.
Barry Mendelow
Affiliation:
University of the Witwatersrand, Johannesburg
Michèle Ramsay
Affiliation:
University of the Witwatersrand, Johannesburg
Nanthakumarn Chetty
Affiliation:
University of the Witwatersrand, Johannesburg
Wendy Stevens
Affiliation:
University of the Witwatersrand, Johannesburg
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Summary

INTRODUCTION

The cell is a dynamic system – a vast array of inter acting molecules forming complex metabolic networks in continuous motion. Proteins are the active molecules transforming the information encoded in genomic DNA into function, enabling and regulating cell life – division, differentiation, communication – and death.

The complement of proteins within a cell at any given time may exceed 400 000. These molecules have many diverse roles. They may be extracellular messengers, such as hormones or growth factors, they may be ion channels or membrane receptors for hormones, growth factors or neurotransmitters, they may function as enzymes or response elements within the cell, or they may be regulators of nuclear transcription. In medicine, most of the differences between tissues in health and disease are seen at the protein level.

In this chapter, we will focus on the cell cycle, cell division and differentiation, and programmed cell death or apoptosis. We will explore the cellular communication networks that regulate these processes and consider the actions of certain of the proteins involved in the systems. But first, because it is such an important mechanism in the control of cellular activity, we begin with a brief discussion of protein phosphorylation.

PROTEIN PHOSPHORYLATION

The presence of phosphate in protein molecules was known more than a century ago but only in the 1950s, as a result of independent studies of Sutherland and co-workers and Fischer and Krebs, was its vital functional importance recognised. Since that time, more and more phosphate-containing proteins, protein kinases and phosphoprotein phosphatases continued to be identified at an everincreasing rate.

The reversible phosphorylation of proteins influences virtually all cellular functions and is an essential mechanism in the control of life processes. Many proteins are activated or inactivated by the simple transfer of a phosphate group from one molecule to another. Some proteins are activated by phosphorylation while others are inactivated.

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Publisher: Wits University Press
Print publication year: 2008

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  • Molecular Cell Biology
    • By Natalie A Whalley, PhD, lectures in the Division of Molecular Medicine and Haematology, School of Pathology, University of the Witwatersrand., Sarah Walters, BSc (Hons), MSc (Med) (Genetic Counselling), worked as a genetic counsellor in the Division of Human Genetics, University of the Witwatersrand, from 2001 to 2007. In 2007 she became Honorary Treasurer of the Southern African Inherited Disorders Association and began setting up the Birth Defects and Disabilities Foundation (BDDF). She is currently coordinator of the BDDF and programme director of the Medical Genetics Education Programme for registered nurses., Kate Hammond, BSc (Hons), MT, PhD, is Professor of Molecular Medicine and Haematology, University of the Witwatersrand.
  • Edited by Barry Mendelow, University of the Witwatersrand, Johannesburg, Michèle Ramsay, University of the Witwatersrand, Johannesburg, Nanthakumarn Chetty, University of the Witwatersrand, Johannesburg, Wendy Stevens, University of the Witwatersrand, Johannesburg
  • Book: Molecular Medicine for Clinicians
  • Online publication: 04 June 2019
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  • Molecular Cell Biology
    • By Natalie A Whalley, PhD, lectures in the Division of Molecular Medicine and Haematology, School of Pathology, University of the Witwatersrand., Sarah Walters, BSc (Hons), MSc (Med) (Genetic Counselling), worked as a genetic counsellor in the Division of Human Genetics, University of the Witwatersrand, from 2001 to 2007. In 2007 she became Honorary Treasurer of the Southern African Inherited Disorders Association and began setting up the Birth Defects and Disabilities Foundation (BDDF). She is currently coordinator of the BDDF and programme director of the Medical Genetics Education Programme for registered nurses., Kate Hammond, BSc (Hons), MT, PhD, is Professor of Molecular Medicine and Haematology, University of the Witwatersrand.
  • Edited by Barry Mendelow, University of the Witwatersrand, Johannesburg, Michèle Ramsay, University of the Witwatersrand, Johannesburg, Nanthakumarn Chetty, University of the Witwatersrand, Johannesburg, Wendy Stevens, University of the Witwatersrand, Johannesburg
  • Book: Molecular Medicine for Clinicians
  • Online publication: 04 June 2019
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Molecular Cell Biology
    • By Natalie A Whalley, PhD, lectures in the Division of Molecular Medicine and Haematology, School of Pathology, University of the Witwatersrand., Sarah Walters, BSc (Hons), MSc (Med) (Genetic Counselling), worked as a genetic counsellor in the Division of Human Genetics, University of the Witwatersrand, from 2001 to 2007. In 2007 she became Honorary Treasurer of the Southern African Inherited Disorders Association and began setting up the Birth Defects and Disabilities Foundation (BDDF). She is currently coordinator of the BDDF and programme director of the Medical Genetics Education Programme for registered nurses., Kate Hammond, BSc (Hons), MT, PhD, is Professor of Molecular Medicine and Haematology, University of the Witwatersrand.
  • Edited by Barry Mendelow, University of the Witwatersrand, Johannesburg, Michèle Ramsay, University of the Witwatersrand, Johannesburg, Nanthakumarn Chetty, University of the Witwatersrand, Johannesburg, Wendy Stevens, University of the Witwatersrand, Johannesburg
  • Book: Molecular Medicine for Clinicians
  • Online publication: 04 June 2019
Available formats
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