Book contents
- Frontmatter
- Contents
- Preface
- List of Abbreviations
- Part I Introduction and Background
- 1 Motivation and Outline
- 2 Biochemistry for Engineers: A Short Primer
- 3 Engineered Artificial Membranes
- Part II Building Engineered Membranes, Devices, and Experimental Results
- Part III Dynamic Models for Artificial Membranes: From Atoms to Device
- Appendices
- Bibliography
- Index
1 - Motivation and Outline
from Part I - Introduction and Background
Published online by Cambridge University Press: 25 May 2018
- Frontmatter
- Contents
- Preface
- List of Abbreviations
- Part I Introduction and Background
- 1 Motivation and Outline
- 2 Biochemistry for Engineers: A Short Primer
- 3 Engineered Artificial Membranes
- Part II Building Engineered Membranes, Devices, and Experimental Results
- Part III Dynamic Models for Artificial Membranes: From Atoms to Device
- Appendices
- Bibliography
- Index
Summary
In simple terms a biological membrane consists of two layers of fat that slide on each other – hence membranes are called lipid bilayers. Biological membranes include more than just the cell membrane. Within the cell, there are several structures that are bound by membranes; these structures are called organelles and include the nucleus, mitochondria, endoplasmic reticulum, Gogli apparatus, and lysomes.
Why Membranes?
Why biological membranes? Membranes and the macromolecules embedded in them perform extremely important biological functions. They form selectively permeable barriers that enclose cells and organelles within the cell. The cell membrane is the target of physical, chemical, and biological agents such as thermal and mechanical stress, toxins, hormones, viruses, and microbes.
Biological membranes exhibit remarkable properties. Embedded in the membrane are protein macromolecules that perform crucial functions for a living cell. For example, ion channels are subnanosized pores formed out of proteins in the membrane that selectively open and close and allow ions to flow into the cell. It is known that almost 25 percent of genes code for membrane proteins. Also, more than 50 percent of available drugs target membrane proteins [369]. Cytoskeletal filaments and sterols, such as cholesterol, give structural stability to the membrane. Antimicrobial drugs bind to specific sites in the membrane of bacterial cells and induce pores in the membrane that compromise the integrity of the membrane and lead to bacterial cell death. Applying a voltage across a membrane causes the membrane to spontaneously form pores – this process is called electroporation and is crucial for drug delivery mechanisms. A membrane has several moving parts that comprise lipids and macromolecules that perform a variety of biological tasks. For example, the assembly of new cellular membranes commonly results from old membranes in which membrane-bound enzymes construct new lipid molecules. These new lipid molecules then either diffuse into the old membrane or form vesicles which can merge with other membranes via vesicle fusion. Vesicle fusion requires the coordination of several proteins and macromolecules as biological membranes do not spontaneously fuse. The process of vesicle fusion and cellular membrane assembly is still an active area of research.
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- Publisher: Cambridge University PressPrint publication year: 2018