The following sections of this BookRags Literature Study Guide is offprint from Gale's For Students Series: Presenting Analysis, Context, and Criticism on Commonly Studied Works: Introduction, Author Biography, Plot Summary, Characters, Themes, Style, Historical Context, Critical Overview, Criticism and Critical Essays, Media Adaptations, Topics for Further Study, Compare & Contrast, What Do I Read Next?, For Further Study, and Sources.
(c)1998-2002; (c)2002 by Gale. Gale is an imprint of The Gale Group, Inc., a division of Thomson Learning, Inc. Gale and Design and Thomson Learning are trademarks used herein under license.
The following sections, if they exist, are offprint from Beacham's Encyclopedia of Popular Fiction: "Social Concerns", "Thematic Overview", "Techniques", "Literary Precedents", "Key Questions", "Related Titles", "Adaptations", "Related Web Sites". (c)1994-2005, by Walton Beacham.
The following sections, if they exist, are offprint from Beacham's Guide to Literature for Young Adults: "About the Author", "Overview", "Setting", "Literary Qualities", "Social Sensitivity", "Topics for Discussion", "Ideas for Reports and Papers". (c)1994-2005, by Walton Beacham.
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Complement refers to a series of some 30 proteins that enhance the bacterial killing effect of antibodies. This complementation involves facilitating the engulfing of bacteria by immune cells in the process known as phagocytosis, or by the puncturing of the bacterial membrane. Additionally, complement helps dispose of antigen-antibody complexes that form in the body.
The various complement proteins circulate throughout the bloodstream in an inactive form. When one of the proteins is converted to an active form upon interaction with an antigen-antibody complex, a series of reactions is triggered. The activation step involves the cleaving, or precise cutting, of the particular complement protein. The cleavage turns the complement protein into a protease, a protein that is itself capable of cleaving other proteins. In turn, cleavage of a second complement protein makes that protein a protease. The resulting cleavage reaction generates a series of active complement proteins. These reactions, known as the complement cascade, occur in an orderly sequence and are under precise regulation.
The reactions involve two pathways. One is known as the classical complement activation pathway. The end result is an enzyme that can degrade a protein called C3. The other pathway is known as the alternative pathway. The second pathway does not require the presence of antibody for the activation of complement. Both pathways result in the formation of an entity that is called the membrane attack complex. The complex is actually a channel that forms in the bacterial membrane. Under the magnification of the electron microscope, a bacterial membrane that is a target of the complement system appears riddled with holes.
The channels that form in a membrane allow the free entry and exit of fluids and molecules. Because the concentration of various ions is higher inside the bacterium than outside, fluid will flow inward to attempt to balance the concentrations. As a result, the bacterium swells and bursts.
Other reaction products of the complement cascade trigger an inflammatory immune response. In addition, the invading bacteria are coated with an immune molecule (C3b) that makes the bacteria more recognizable to phagocytes. This process is called opsonization. The phagocytes then engulf the bacteria and degrade them.
Tight control over the activity of the complement system is essential. At least 12 proteins are involved in the regulation of complement activation. Defects in this control, or the operation of the pathways, result in frequent bacterial infections.