Biotechnology
Selective Estrogen Receptor Modulators
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- Self-Assembly (of a large molecular struc- ture)
- Semisynthetic Catalytic Antibody
- Senior Advisory Group on Biotechnology (SAGB)
- Sense
- Septic Shock See SEPSIS . Sequence (of a DNA molecule)
- Sequence (of a protein molecule)
- Sequencing (of DNA molecules)
- Sequencing (of oligosaccharides) See RESTRIC- TION ENDOGLYCOSIDASES , SEQUENCE MAP . Sequencing (of protein molecules)
- Serologist See SEROLOGY . Serology
- Seronegative
- Serum
- Signal Transducers and Activators of Tran- scription (STATs)
- Signaling Protein See SIGNALING MOLECULE . Silencing See GENE SILENCING . Silent Mutation
- Simple Sequence Repeat (SSR) DNA Marker Technique
- Single-Cell Protein (SCP)
Selective Estrogen Receptor Modulators Abbreviated SERM. This term refers to chemical compounds (isoflavones, the phar- maceuticals Evista/raloxifene and tamox- ifen, etc.) which impart some beneficial effect on the human body when consumed by humans, without any of the adverse impacts of estrogen (e.g., promotion of the growth of certain tumors by estrogen). See also SELECTIVE ESTROGEN EFFECT , ESTROGEN , ISOFLAVONES , PHYTOCHEMICALS . Self-Assembly (of a large molecular struc- ture) The essentially automatic ordering and assembly of certain molecules into a large structure. Examples of such large molecular structures (often called supramolecular © 2002 by CRC Press LLC S structures or supramolecular assemblies) include micelles, reverse micelles, ribosomes, peptide nanotubes, and Tobacco Mosaic Virus (TMV). The first discovery of a self-assembling active biological structure occurred in 1955, when Heinz Frankel-Conrat and Robley Wil- liams showed that TMV will reassemble into functioning, infectious virus particles (after TMV has been dissociated into its compo- nents via immersion in concentrated acetic acid). In the future, it is hoped that man will be able to “direct” the self-assembly of molecular structures which will: • Serve as “cages” to carefully protect and deliver sensitive/unstable pharmaceuti- cals to targeted tissues within the body. • Serve as “crucibles” (i.e., reaction ves- sels) for small-scale chemical reactions to occur within. • Serve as computer logic or memory devices (i.e., bioelectronics). • Serve as antibiotics. For example, during the 1990s, M. Reza Ghadiri created “peptide nanotubes” made via self-assembly of certain peptides into tubes (cylinders) of nanometer dimensions. These peptide nanotubes are “membrane active” (i.e., insert one end of themselves into the outer membrane of a cell), and cause the cell (e.g., pathogenic bacteria) contents to “leak out,” which kills the bacteria. See also MICELLE , REVERSE MICELLE ( RM ), RIBOSOMES , TOBACCO MOSAIC VIRUS ( TMV ), NANOCRYSTAL MOLECULES , NANOSCIENCE , NANOTECHNOLOGY , NANOMETERS ( NM ), BIOELECTRONICS , ANTIBIOTIC , PATHOGEN , BACTERIA . Semisynthetic Catalytic Antibody An anti- body produced (e.g., via monoclonal anti- body techniques) in response to a carefully selected antigen (i.e., one of the molecules involved in the chemical reaction that you are trying to catalyze). Such an antibody is then made to be catalytic by “attaching” a (molecular) group that is known to catalyze the desired chemical reaction. This attaching is done either via chemical modification of the antibody, or via genetic engineering of the cell (DNA) that produces that antibody. See also CATALYST , ANTIBODY , CATALYTIC ANTIBODY , SITE - DIRECTED MUTAGENESIS ( SDM ), MONOCLONAL ANTIBODIES ( MA b ), ANTIGEN , GENETIC ENGINEERING , ABZYMES . Senior Advisory Group on Biotechnology (SAGB) An association of approximately 35 of the largest European companies that are engaged in at least some form of genetic engineering research or production. Similar to America’s Biotechnology Industry Orga- nization (BIO), the SAGB works with gov- ernments and the public to promote safe and rational advancement of genetic engineering and biotechnology. It was formed in 1989 and is based in Brussels, Belgium. See also BIOTECHNOLOGY , GENETIC ENGINEERING , RECOM- BINANT DNA ( r DNA ), JAPAN BIO - INDUSTRY ASSO- CIATION , INTERNATIONAL FOOD BIOTECHNOLOGY COUNCIL ( IFBC ), BIOTECHNOLOGY INDUSTRY ORGANIZATION ( BIO ). Sense Normal (forward) orientation of DNA sequence (gene) in genome. See also GENE SILENCING , ANTISENSE ( DNA SEQUENCE ). Sepsis Also known as systemic inflammatory response syndrome, this life-threatening condition (“septic shock”) occurs when the body’s immune system over-responds to infection (e.g., by gram-negative bacteria) in which release of bacterial endotoxin (lipopolysaccharide, or LPS) occurs. Those immune system cells (e.g., macrophages, etc.) overproduce numerous inflammatory agents (e.g., cytokines), which induce fever, shock, and sometimes organ failure. See also GRAM - NEGATIVE ( G -), BACTERIA , CYTOKINES , ENDOTOXIN , MACROPHAGE . Septic Shock See SEPSIS . Sequence (of a DNA molecule) The specific nucleic acids that comprise a given segment of a DNA molecule. See also DEOXYRIBO- NUCLEIC ACID ( DNA ), GENETIC CODE , GENE , CHROMOSOMES , NUCLEIC ACIDS , CONTROL SEQUENCES , SEQUENCING ( OF DNA MOLECULES ), STRUCTURAL GENOMICS , COMPLEMENTARY ( MOLECULAR GENETICS ). Sequence (of a protein molecule) The specific amino acids (and the order in which they are coupled together) that comprise a given seg- ment of a protein molecule. See also PROTEIN , AMINO ACID , STRUCTURAL GENE , GENOMICS , © 2002 by CRC Press LLC S STRUCTURAL GENOMICS , SEQUENCING ( OF PROTEIN MOLECULES ). Sequence Map A pictorial representation of the sequence of amino acids in a protein molecule, the sequence of nucleic acids in a DNA molecule, or the sequence of oligosac- charide components in a glycoprotein/carbo- hydrate molecule. See also SEQUENCING ( OF DNA MOLECULES ), SEQUENCING ( OF PROTEIN MOL- ECULES ), SEQUENCING ( OF OLIGOSACCHARIDES ), SEQUENCE ( OF A DNA MOLECULE ), SEQUENCE ( OF A PROTEIN MOLECULE ), RESTRICTION MAP . Sequencing (of DNA molecules) The process used to obtain the sequential arrangement of nucleotides in the DNA backbone. The cleavage into fragments (followed by sepa- ration of those fragments, which can then be sequenced individually) of DNA molecules by one of several methods: (1) a chemical cleavage method followed by polyacryla- mide gel electrophoresis (PAGE) or capillary electrophoresis, (2) a method consisting of controlled interruption of enzymatic replica- tion methods followed by PAGE, (3) a didexyl method utilizing fluorescent “tag” atoms attached to the DNA fragments, fol- lowed by use of spectrophotometry to iden- tify the respective DNA fragments by their differing “tags” (which fluoresce at different wavelengths). This (fluorescent tag) variant of the dideoxy method can be automated to “decipher” large DNA molecules (i.e., genomes). Such automated machines are sometimes called “gene machines.” Sequencing of DNA was first done in the mid-1970s by Frederick Sanger. See also POLYACRYLAMIDE GEL ELECTROPHORESIS ( PAGE ), GENE MACHINE , DEOXYRIBONUCLEIC ACID ( DNA ), SEQUENCE ( OF A DNA MOLECULE ), BASE EXCISION SEQUENCE SCANNING ( BESS ), SHOTGUN SEQUENC- ING , NANOPORE , NEAR - INFRARED SPECTROSCOPY ( NIR ), COMPARATIVE SEQUENCING , BIOCHIPS . Sequencing (of oligosaccharides) See RESTRIC- TION ENDOGLYCOSIDASES , SEQUENCE MAP . Sequencing (of protein molecules) The pro- cess used to obtain the sequential arrange- ment of amino acids in a protein molecule. See also PROTEIN , AMINO ACID , SEQUENCE ( OF A PROTEIN MOLECULE ). Sequon A (potential) site on a protein mole- cule’s “backbone” where a sugar molecule (or a chain of sugar molecules, i.e., an oligo- saccharide) may be attached. See also PROTEIN , SUGAR MOLECULES , GLYCOPROTEIN , GLYCOGEN , G L Y C O S Y L A T I O N , P R O T E I N E N G I N E E R I N G , OLIGOSACCHARIDES . Serine (ser) A nonessential amino acid; a bio- synthetic precursor of several metabolites, including cysteine, glycine, and choline. In 1999, Solomon H. Snyder, Herman Wolosker, and Seth Blackshaw conducted research that showed that some mammals synthesize (manufacture) D -serine within their brains, and it functions as a neurotrans- mitter there. See also ESSENTIAL AMINO ACIDS , METABOLITE , CYSTEINE ( cys ), GLYCINE ( G ly ), CHOLINE , NEUROTRANSMITTER . Seroconversion The development of antibod- ies (specific to that disease-causing microor- ganism) in response to vaccination or natural exposure to a disease-causing microorgan- ism. See also SEROLOGY , ANTIBODY , IMMUNO- GLOBULIN , HUMORAL IMMUNITY , PATHOGEN , POLYCLONAL ANTIBODIES , PASSIVE IMMUNITY . Serologist See SEROLOGY . Serology A subdiscipline of immunology, con- cerned with the properties and reactions of blood sera. It includes the diverse techniques used for the “test tube” measurement of anti- body-antigen reactions, including blood typ- ing (e.g., for transfusions). See also MAJOR HISTOCOMPATIBILITY COMPLEX ( MHC ), OLIGO- SACCHARIDES , SERUM LIFETIME . Seronegative Refers to negative results of a serology test. See also SEROLOGY , HUMORAL IMMUNITY , ANTIBODY . Serotonin An important neurochemical whose effects upon the human brain include mood elevation. Production of serotonin in the brain is increased by ingestion of the amino acid tryptophan (a chemical precursor to serotonin). Elevation of brain levels of sero- tonin can also be caused by consumption of the herb known as Saint John’s Wort (Hypericum perforatum), or by consumption of certain pharmaceuticals such as the anti- depressants Prozac™ (trademarked product of Eli Lilly & Company), Zoloft™ (trade- marked product of Pfizer, Inc.), or Paxil™ (trademarked product of Smithkline Beecham PLC). In 1997, Marianne Regard and Theodor Landis discovered that humans © 2002 by CRC Press LLC S afflicted with hemorrhagic lesions in the brain (cause of abnormal serotonin activa- tion/production) often became “passionate culinary afficionados.” See also TRYPTOPHAN ( trp ), ESSENTIAL AMINO ACIDS , BLOOD - BRAIN BARRIER ( BBB ), NEUROTRANSMITTER . Serotypes A variety (sub-strain) of a microor- ganism that is distinguished from others (in the strain) via its serological effects (within immune system of the host organism it inhabits). See also BACTERIA , STRAIN , E . COLI 0157 : H 7 , SEROLOGY , HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 ( HIV- 1 ), HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 ( HIV- 2 ). Serum Blood plasma that has had its clotting factor removed. See also FACTOR VIII , FACTOR IX , PLASMA . Serum Half Life See SERUM LIFETIME . Serum Immune Response See HUMORAL IMMU- NITY . Serum Lifetime The average length of time that a molecule circulates in an organism’s bloodstream before it is cleared from the bloodstream. See also IMMUNE RESPONSE , ANTIGEN . Sessile (Micro)organisms that are attached to a (support) substrate directly by their base; not attached via an intervening peduncle (i.e., stalk). Can also refer to fruit or leaves that are attached directly to the main stem or branch of a plant. See also VAGILE . Sex Chromosomes T h o s e c h r o m o s o m e s whose content is different in the two sexes of a given species. They are usually labeled X and Y (or W and Z); one sex has XX (or WW), the other sex has XY (or WZ). XX (WW) is female and XY (WZ) is male. Sexual Conjugation An infrequent occurrence in which two adjacent bacteria stretch out por- tions of their (cell) membranes to touch one another, fuse, and then pass transposons, jumping genes, or plasmids to each other. See also ASEXUAL , BACTERIA , CELL , CONJUGATION , PLASMID , TRANSPOSON , JUMPING GENES . Shotgun Cloning Method A technique for obtaining the desired gene that involves “chopping up” the entire genetic complement of a cell using restriction enzymes, then attaching each (resultant) DNA fragment to a vector and transferring it into a bacterium, and finally screening those (engineered) bacteria to locate the bacteria that are producing the desired product (e.g., a protein). See also GENETIC ENGINEERING , GENOME , RESTRICTION ENDONUCLEASES , VECTOR . Shotgun Sequencing Sometimes called Whole- genome Shotgun Sequencing. A technology for rapid sequencing of DNA, in which an organism’s genome (DNA) is first frag- mented (“broken up”), and then randomly selected pieces of the DNA are individually sequenced. Those individual pieces’ sequences must subsequently be “bridged” (i.e., “assembled” in an overlapping end-by- end pattern) in order to assemble a complete map (e.g., of an organism’s chromosome or genome). See also SEQUENCING ( OF DNA MOL- ECULES ), DEOXYRIBONUCLEIC ACID ( DNA ), SEQUENCE ( OF A DNA MOLECULE ), GENOME , DNA “ BRIDGES ”, CHROMOSOME , GENETIC MAP . Shuttle Vector A vector capable of replicating in two unrelated species. See also VECTOR , REPLICATION ( OF VIRUS ). Signal Transducers and Activators of Tran- scription (STATs) Molecules that cause signal transduction to occur (i.e., when a hormone or other chemical “binds” to it), or molecules that cause transcription to occur (i.e., when transcription factor(s) “bind” to it). STATs can be attached to solid surfaces (e.g., in a bioassay or biosensor) for use in such research applications as high-through- put screening. See also SIGNAL TRANSDUCTION , HORMONE , TRANSCRIPTION FACTORS , BIOCHIPS , BIOSENSORS ( ELECTRONIC ), BIOASSAY , HIGH - THROUGHPUT SCREENING ( HTS ), MICROARRAY ( TESTING ), TARGET ( OF A HERBICIDE OR INSECTI- CIDE ), CASCADE . Signal Transduction The “reception” and “conversion” of a “chemical message” (e.g., hormone) by a cell. For example, G-proteins (which are embedded in the surface mem- brane of certain cells, but extend through to outside and inside of the membrane) accom- plish signal transduction. When a hormone, drug, neurotransmitter, or other signal chem- ical binds (i.e., “docks”) to the receptor (on the exterior of the cell’s plasma membrane), the receptor activates the G-protein, causing an effector inside cell to produce a “signal” © 2002 by CRC Press LLC S chemical inside the cell, which then reacts to the original external chemical signal received. See also CELL , PLASMA MEMBRANE , TRANSMEMBRANE PROTEINS , RECEPTORS , EGF RECEPTOR , RAS GENE , NUCLEAR RECEPTORS , SIG- NALING , G - PROTEINS , MAST CELLS , CD 95 PROTEIN , HORMONE , SUBSTANCE P , LECITHIN , CASCADE . Signaling The “communication” that occurs between and within cells of an organism, e.g., via hormones, nitric acid, etc. Such signaling “tells” certain cells to grow, change, or pro- duce specific proteins at specific times. See also RECEPTORS , PROTEIN , NUCLEAR RECEPTORS , G - PROTEINS , SIGNAL TRANSDUCTION ( SIGNAL ), TRANSDUCTION ( GENE ), CD 95 PROTEIN , HORMONE , PARKINSON ’ S DISEASE , HARPIN , SUBSTANCE P , LECITHIN , NITRIC OXIDE , SIGNAL TRANSDUCERS AND ACTIVATORS OF TRANSCRIPTION ( STAT s ), PROTEIN SIGNALING , CASCADE , CHOLINE . Signaling Molecule A molecule utilized to “signal” (communicate) with cells, or to deliver a signal to other organisms (e.g., a signal by the soybean plant to attract bene- ficial Rhizobium bacteria to colonize the roots of that soybean plant). For example, the young offspring of fleas can remain immature (larvae) for up to 2 years in the absence of a food source, until carbon dioxide molecules and heat from a nearby mammal (potential host/food source) signal them to mature into adults in order to prey on the mammal. Another example: the larvae of North American tree frogs are signaled by chemicals released into a pond’s water when the first such frog larva is killed by a (preda- tory) dragonfly nymph (i.e., when those drag- onflies first arrive each year at a given pond, to prey on the frog larvae). That chemical “signal” causes all of the North American tree frog larvae in that pond to subsequently grow tails that are twice as large as were grown by them prior to that chemical signal, to facilitate their escape from the dragonfly nymphs. See also SIGNALING , NITRIC OXIDE , G-PROTEINS , HOR- MONE , SUBSTANCE P , LEUKOTRIENES , ISOFLA- VONES , SOYBEAN PLANT , RHIZOBIUM ( BACTERIA ), HARPIN , OCTADECANOID / JASMONATE SIGNAL COM- PLEX , SALICYCLIC ACID ( SA ). Signaling Protein See SIGNALING MOLECULE . Silencing See GENE SILENCING . Silent Mutation A mutation in a gene that causes no detectable change in the biological characteristics of that gene’s product (e.g., a protein). See also EXPRESS , GENE , PROTEIN . Silk A natural, protein polymer with a predom- inance of alanine and glycine amino acids. Silk is produced by silkworms that have fed on mulberry tree leaves. The body of a silk- worm can retain proteins (i.e., raw material for silk) amounting to as much as 20% of its body weight. It is thought that silk may be altered, via genetic engineering of silk- worms, to produce fibers of very high strength. See also GENETIC ENGINEERING , PRO- TEIN ENGINEERING , AMINO ACID . Simple Protein A protein that yields only amino acids on hydrolysis (i.e., cleavage of the protein molecule into fragments), and does not have other molecular constituents such as lipids or polysaccharide attachments. See also PROTEIN , AMINO ACID , GLYCOPROTEIN , LIPIDS , POLYSACCHARIDES . Simple Sequence Repeat (SSR) DNA Marker Technique A “genetic mapping” technique which utilizes the fact that microsatellite sequences “repeat” (appear repeatedly in sequence within the DNA molecule) in a manner enabling them to be used as “mark- ers.” See also GENETIC MAP , SEQUENCE ( OF A DNA MOLECULE ), RANDOM AMPLIFIED POLYMOR- PHIC DNA ( RAPD ) TECHNIQUE , RESTRICTION FRAG- MENT LENGTH POLYMORPHISM ( RFLP ) TECHNIQUE , DEOXYRIBONUCLEIC ACID ( DNA ), PHYSICAL MAP ( OF GENOME ), LINKAGE , LINKAGE GROUP , MARKER ( GENETIC MARKER ), LINKAGE MAP , TRAIT , MICRO- SATELLITE DNA , QUANTITATIVE TRAIT LOCI ( QTL ). Single-Cell Protein (SCP) Protein derived from single-celled organisms with a high protein content. Yeast is an example. Gener- ally used in regard to those organisms that are edible by domesticated animals or humans. Single-Domain Antibodies (dAbs) VH “heavy chains” (portion of antibody molecules) produced by genetically engi- neered Escherichia coli cells that act to bind antigens in a manner similar to antibodies or monoclonal antibodies (MAbs). Similar to MAbs, dAbs can be produced in large quan- tities, to be used as human or animal thera- peutics (e.g., to combat diseases). See also © 2002 by CRC Press LLC S ANTIBODY , MONOCLONAL ANTIBODIES ( MA b ), ANTIGEN , ESCHERICHIA COLI . Single-nucleotide Polymorphisms (SNPs) Variations (in individual nucleotides) that occur within DNA at the rate of approxi- mately one in every 1,300 base pairs in most organisms (approximately one in every 100 base pairs in humans’ DNA). SNPs usually occur in the same genomic location (e.g., on the organism’s DNA) in different individu- als. These variations account for: • Diversity within a given species (e.g., black cattle and white cattle, different strains/serotypes within a given bacte- ria species, etc.) • Some genetic diseases [e.g., the disease cystic fibrosis is due to one SNP, the disease known as familial dysautono- mia is due to one SNP, the disease known as (Duchenne) muscular dystro- phy is due to one SNP, etc.] • The body’s response to certain pharma- ceuticals and food ingredients (e.g., the diuretic drug thiazide works to control hypertension in 60% of U.S. African Americans, but only 8% of U.S. Cau- casian people, due to one SNP) Certain pharmaceuticals do not have the desired effect in some groups of humans possessing certain specific “grouped SNPs” known as haplotypes. Because those “group- ings of SNPs” are linked (i.e., tend to “travel together” as a group within the genetics of a given population), they can collectively confer a given “multiple-SNP-trait” to an identifiable subpopulation of individuals. For example, the pharmaceuticals acetami- nophen, aspirin, and Valium remain in the bodies of women (who constitute a haplo- type for that pharmacogenomic trait) longer than in men. Methods utilized to identify SNPs include examination of the DNA of populations of individuals with and without a given (genet- ically related) disease and with and without a given trait. “SNP mapping” is a “genetic mapping” technique that utilizes the fact that individual nucleotides (within a DNA mole- cule) can exist in different forms (for a particular “site”/location on that DNA mol- ecule), which enables such SNPs to be uti- lized as “markers.” One example would be to track a given SNP vs. occurrence of genet- ically related disease in a given human pop- u l a t i o n . S e e a l s o P O I N T M U T A T I O N , DEOXYRIBONUCLEIC ACID ( DNA ), SEQUENCE ( OF A DNA MOLECULE ), NUCLEOTIDE , POLYMORPHISM ( GENETIC ), GENETICS , GENETIC MAP , PHYSICAL MAP ( OF GENOME ), GENOME , TRAIT , MARKER ( GENETIC MARKER ), QUANTITATIVE TRAIT LOCI ( QTL ), DIVERSITY ( WITHIN A SPECIES ), BASE PAIR ( bp ), TRANSVERSION , CYSTIC FIBROSIS TRANS- MEMBRANE REGULATOR PROTEIN ( CFTR ), MUSCU- LAR DYSTROPHY ( MD ), PHARMACOGENETICS , PHARMACOGENOMICS , HAPLOTYPE , SNP MAP , TOXICOGENETICS , ORGANISM . Download 4.84 Kb. Do'stlaringiz bilan baham: |
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