Large Biological Molecules: Structure and Function

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Comprehensive vocabulary flashcards covering the structure, synthesis, and functions of carbohydrates, lipids, proteins, and nucleic acids.

96 Terms

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Macromolecules

Giant molecules composed of thousands of covalently connected atoms, comprising three classes of large biological molecules: carbohydrates, proteins, and nucleic acids.

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Polymer

A long molecule consisting of many similar or identical building blocks linked by covalent bonds.

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Monomers

The repeating small building-block molecules that serve as the subunits of a polymer.

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Dehydration Reaction

A reaction in which two monomers become covalently bonded to each other with the loss of a water molecule; also known as a condensation reaction.

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Hydrolysis

A chemical reaction that breaks bonds between monomers in a polymer through the addition of a water molecule, functioning as the reverse of a dehydration reaction.

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Enzymes

Macromolecules that act as catalysts to selectively speed up chemical reactions without being consumed by them.

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Monosaccharides

The simplest carbohydrates, or single sugars, that generally have molecular formulas that are multiples of the unit CH2O\text{CH}_2\text{O}.

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Aldose

A sugar classified by having a carbonyl group located at the end of the carbon skeleton (an aldehyde sugar), such as glucose and galactose.

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Ketose

A sugar classified by having a carbonyl group located within the interior of the carbon skeleton (a ketone sugar), such as fructose and ribulose.

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Disaccharide

A double sugar consisting of two monosaccharides joined by a covalent glycosidic linkage formed via a dehydration reaction.

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Glycosidic Linkage

A covalent bond formed between two monosaccharides by a dehydration reaction.

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Polysaccharides

Macromolecules formed from polymers of hundreds to thousands of monosaccharides joined by glycosidic linkages, functioning in energy storage or structural support.

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Starch

A plant storage polysaccharide consisting entirely of glucose monomers connected by α\alpha 1–4 glycosidic linkages, stored as granules in plastids such as chloroplasts.

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Glycogen

An extensively branched storage polysaccharide of glucose found in animals, primarily stored in liver and muscle cells.

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Cellulose

A structural polysaccharide consisting of straight, unbranched chains of β\beta glucose monomers linked by β\beta 1–4 glycosidic linkages, serving as a primary component of plant cell walls.

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Microfibrils

Cable-like units of parallel cellulose molecules held together by hydrogen bonds between hydroxyl groups, conferring high tensile strength to plant cell walls.

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Chitin

A structural polysaccharide containing an amino sugar derivative, found in the exoskeletons of arthropods and in the cell walls of many fungi.

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Lipids

A diverse class of large biological molecules that do not consist of polymers and are hydrophobic due to a high proportion of nonpolar hydrocarbon bonds.

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Fat (Triacylglycerol)

A lipid composed of three fatty acid molecules linked to a three-carbon glycerol molecule by ester linkages; also called a triglyceride.

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Fatty Acid

A molecule consisting of a long hydrocarbon skeleton with a carboxyl group at one end.

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Saturated Fatty Acid

A fatty acid in which all carbons in the hydrocarbon chain are joined by single bonds, allowing the maximum number of hydrogen atoms to be bonded to the skeleton.

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Unsaturated Fatty Acid

A fatty acid possessing one or more double bonds in the hydrocarbon chain, typically causing a kink or bend in the chain's shape due to a cis configuration.

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Hydrogenation

The synthetic process of converting unsaturated fats into saturated fats by chemically adding hydrogen, which often generates trans fats as a byproduct.

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Trans Fats

Unsaturated fats with trans double bonds produced during the industrial hydrogenation of vegetable oils, which can contribute to cardiovascular disease.

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Phospholipid

An amphipathic lipid made of a glycerol molecule joined to two fatty acids and a phosphate group, forming hydrophobic tails and a hydrophilic head.

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Steroids

A class of lipids characterized by a carbon skeleton composed of four fused carbon rings with attached functional groups.

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<p>Cholesterol</p>

Cholesterol

A steroid that forms an essential component of animal cell membranes and serves as the precursor for synthesize of other steroid molecules.

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Polypeptides

Unbranched polymers built from amino acids linked by peptide bonds that make up the structural units of proteins.

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<p>Amino Acid</p>

Amino Acid

An organic monomer containing both an amino group (−NH2-\text{NH}_2) and a carboxyl group (−COOH-\text{COOH}), along with a variable side chain (R\text{R} group).

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Peptide Bond

The covalent bond formed between the carboxyl group of one amino acid and the amino group of an adjacent amino acid via a dehydration reaction.

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Primary Structure

The unique, genetically determined linear sequence of amino acids in a polypeptide chain.

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Secondary Structure

The localized, repetitive coiling or folding of the polypeptide backbone, stabilized by hydrogen bonds between the constituents of the backbone.

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α\alpha Helix

A delicate coil-shaped secondary protein structure held together by hydrogen bonds between every fourth amino acid in the polypeptide backbone.

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β\beta Pleated Sheet

A secondary protein structure formed when two or more segments of a polypeptide chain lie parallel or antiparallel to each other, stabilized by hydrogen bonds between the backbones.

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Tertiary Structure

The overall three-dimensional shape of a polypeptide resulting from interactions between the variable side chains (R\text{R} groups) of the amino acids.

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Disulfide Bridges

Strong covalent linkages between the sulfur atoms of two cysteine side chains (−CH2−S−S−CH2−-\text{CH}_2-\text{S}-\text{S}-\text{CH}_2-) that reinforce tertiary structure.

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Quaternary Structure

The structural level resulting from the association and aggregation of two or more distinct polypeptide subunits into a single functional macromolecule.

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Denaturation

The process where a protein unravels and loses its native native shape due to disruptions in hydrogen bonds, ionic bonds, or other interactions caused by extremes in pH, salt concentration, or temperature.

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<p>Chaperonins</p>

Chaperonins

Multi-protein complexes that assist in the proper folding of other proteins by sheltering them from damaging chemical environments in the cytoplasm.

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X-ray Crystallography

A technique used to determine the three-dimensional atomic structure of biological molecules by analyzing the diffraction pattern of an X-ray beam passed through a crystal.

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Gene

A discrete unit of inheritance that programs the amino acid sequence of a polypeptide, consisting of a specific segment of DNA.

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Nucleic Acids

Polymers made of nucleotide monomers that serve as molecules for storing, transmitting, and expressing genetic hereditary information.

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Nucleotide

The building-block monomer of a nucleic acid, consisting of a five-carbon sugar, a nitrogen-containing base, and one or more phosphate groups.

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Nucleoside

The structural portion of a nucleotide that consists only of a nitrogenous base attached to a pentose sugar, lacking any phosphate group.

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Pyrimidines

A family of nitrogenous bases characterized by a single six-membered ring of carbon and nitrogen atoms; includes cytosine (C), thymine (T), and uracil (U).

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Purines

A family of nitrogenous bases characterized by a six-membered ring fused to a five-membered ring; includes adenine (A) and guanine (G).

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Phosphodiester Linkage

The covalent bond that joins adjacent nucleotides along a polynucleotide chain, connecting the −OH-\text{OH} on the 3′3' carbon of one sugar to the phosphate attached to the 5′5' carbon of the next.

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Antiparallel

The arrangement of the two sugar-phosphate backbones in a DNA double helix, running parallel to each other but oriented in opposite 5′→3′5' \rightarrow 3' directions.

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Macromolecules

Large molecules composed of thousands of covalently connected atoms, including carbohydrates, proteins, and nucleic acids.

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Polymer

A long molecule consisting of many similar or identical building blocks linked by covalent bonds.

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Monomer

Small building-block molecules that serve as the repeating units used to build polymers.

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Dehydration Reaction

A reaction (also termed a condensation reaction) in which two monomers become covalently bonded together through the loss of a water molecule.

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Hydrolysis

A chemical reaction that disassembles polymers into monomers, essentially reversing the dehydration reaction by adding a water molecule to break the covalent bond.

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Enzyme

A macromolecule (typically a protein) that serves as a catalyst to selectively speed up chemical reactions without being consumed in the process.

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Monosaccharides

The simplest carbohydrates, or single sugars, which possess molecular formulas that are generally multiples of CH2OCH_2O and serve as major cellular fuel and building material.

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Glycosidic Linkage

A covalent bond formed between two monosaccharides by a dehydration reaction.

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Starch

A plant storage polysaccharide consisting entirely of glucose monomers linked together, stored as granules within chloroplasts and other plastids.

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Glycogen

An extensively branched storage polysaccharide found in animals, stored predominantly in liver and muscle cells.

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Cellulose

A major structural polysaccharide component of tough plant cell walls, consisting of straight, unbranched polymers of β\beta glucose monomers joined by 1−41-4 glycosidic linkages.

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Microfibrils

Parallel arrays of straight cellulose molecules held together by hydrogen bonds between hydroxyl groups and hydrogen atoms, forming strong structural units in plant cell walls.

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Chitin

A structural polysaccharide found in the exoskeletons of arthropods and the cell walls of many fungi, also used to produce strong, flexible surgical thread.

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Lipids

A diverse class of large biological molecules that do not form true polymers and share the unifying feature of being hydrophobic due to nonpolar hydrocarbon structures.

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Triacylglycerol

A fat molecule constructed from one glycerol molecule joined to three fatty acid tails via ester linkages; also known as a triglyceride.

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Saturated Fatty Acid

A fatty acid with a hydrocarbon chain containing no double bonds and having the maximum number of hydrogen atoms possible, typically solidifying at room temperature.

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<p>Unsaturated Fatty Acid</p>

Unsaturated Fatty Acid

A fatty acid possessing one or more double bonds in the hydrocarbon chain (commonly cis double bonds causing kinks), typically remaining liquid at room temperature.

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Hydrogenation

The industrial process of synthetically adding hydrogen to unsaturated fats to convert them into saturated fats, which often creates trans double bonds.

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Trans Fats

Unsaturated fats containing trans double bonds formed during the hydrogenation of vegetable oils, which contribute heavily to cardiovascular disease.

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Phospholipids

Lipids composed of a glycerol molecule joined to two hydrophobic fatty acid tails and a hydrophilic head containing a phosphate group and choline, assembling into cell membrane bilayers.

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<p>Phospholipid Bilayer</p>

Phospholipid Bilayer

A double-layered arrangement formed when phospholipids are added to water, in which hydrophobic fatty acid tails shield themselves by facing inward while hydrophilic phosphate heads contact water.

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Steroids

Lipids characterized by a carbon skeleton consisting of four fused rings with attached chemical functional groups.

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<p>Cholesterol</p>

Cholesterol

An essential steroid lipid found in animal cell membranes and used as a precursor for synthesizing other steroids, though high levels in the blood can contribute to cardiovascular disease.

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Polypeptides

Unbranched polymers constructed from the 20 amino acid monomers, ranging in length from a few to more than a thousand units.

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<p>Amino Acids</p>

Amino Acids

Organic monomers consisting of an asymmetric alpha (α\alpha) carbon bonded to an amino group, a carboxyl group, a hydrogen atom, and a variable side chain (R group).

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Peptide Bond

The covalent bond formed between the carboxyl group of one amino acid and the amino group of another through a dehydration reaction.

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Primary Structure

The unique, genetically determined linear sequence of amino acids in a polypeptide chain.

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Secondary Structure

Repetitive coils and folds within a polypeptide chain formed by hydrogen bonds between repeating constituents of the polypeptide backbone.

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Alpha (α\alpha) Helix

A delicate coiled secondary structure held together by hydrogen bonding between every fourth amino acid along the polypeptide backbone.

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Beta (β\beta) Pleated Sheet

A pleated secondary structure formed by parallel or antiparallel polypeptide backbone strands joined together by hydrogen bonds.

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Tertiary Structure

The overall three-dimensional shape of a polypeptide determined by interactions among variable R groups, including hydrogen bonds, ionic bonds, hydrophobic interactions, and van der Waals interactions.

<p>The overall three-dimensional shape of a polypeptide determined by interactions among variable R groups, including hydrogen bonds, ionic bonds, hydrophobic interactions, and van der Waals interactions.</p>
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Disulfide Bridges

Strong covalent bonds formed when the sulfhydryl groups (−SH-SH) of two cysteine amino acids oxidize to link their sulfur atoms (−S−S−-S-S-), reinforcing tertiary protein structure.

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Quaternary Structure

The overall structural organization resulting from the association and assembly of two or more distinct polypeptide subunits into one functional protein complex.

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Sickle-Cell Disease

An inherited blood disorder caused by a single amino acid substitution (valine substituted for glutamic acid at the 6th position) in the primary structure of hemoglobin, leading to fiber aggregation and deformed red blood cells.

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Denaturation

The unraveling and structural breakdown of a protein caused by adverse changes in pH, salt concentration, temperature, or other environmental factors, resulting in a biologically inactive state.

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<p>Chaperonins</p>

Chaperonins

Multiprotein complexes with a hollow cylinder and cap that create a sheltered hydrophilic chamber to assist the proper folding of unfolded polypeptides.

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X-ray Crystallography

An experimental method used to deduce the three-dimensional atomic structure of proteins and other macromolecules by recording the diffraction pattern of X-rays passed through a crystal.

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Bioinformatics

The computational approach that employs computer programs to model and predict macromolecular structures and relationships based on amino acid or nucleotide sequences.

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Gene

A discrete unit of inheritance made of DNA that programs the primary amino acid sequence of a polypeptide.

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Nucleic Acids

Polymers (polynucleotides) composed of nucleotide monomers that store, transmit, and express hereditary genetic information, encompassing DNA and RNA.

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Nucleotide

A monomer of a nucleic acid, consisting of a nitrogenous base, a five-carbon pentose sugar, and one or more phosphate groups.

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Nucleoside

The portion of a nucleotide unit consisting solely of a nitrogenous base attached to a pentose sugar, without a phosphate group.

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Pyrimidines

A family of nitrogenous bases characterized by a single six-membered ring; includes cytosine (C), thymine (T, in DNA), and uracil (U, in RNA).

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Purines

A family of nitrogenous bases characterized by a six-membered ring fused to a five-membered ring; includes adenine (A) and guanine (G).

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Deoxyribose and Ribose

The pentose sugars of nucleic acids; deoxyribose (present in DNA) lacks an oxygen atom on its 2′2' carbon atom, whereas ribose (present in RNA) possesses a hydroxyl group (−OH-OH) on its 2′2' carbon.

<p>The pentose sugars of nucleic acids; deoxyribose (present in DNA) lacks an oxygen atom on its $$2'$$ carbon atom, whereas ribose (present in RNA) possesses a hydroxyl group ($$-OH$$) on its $$2'$$ carbon.</p>
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Phosphodiester Linkage

The covalent bond that joins adjacent nucleotides in a polynucleotide, connecting the −OH-OH group on the 3′3' carbon of one sugar to the phosphate on the 5′5' carbon of the next.

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Antiparallel

The structural arrangement of the two sugar-phosphate backbones in the DNA double helix, which run side by side in opposite 5′→3′5' \rightarrow 3' directions.

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Biological Macromolecule Linkages

The specific covalent bonds connecting biological monomers: glycosidic linkages for polysaccharides, ester linkages for triacylglycerols, peptide bonds for polypeptides, and phosphodiester linkages for polynucleotides.

<p>The specific covalent bonds connecting biological monomers: glycosidic linkages for polysaccharides, ester linkages for triacylglycerols, peptide bonds for polypeptides, and phosphodiester linkages for polynucleotides.</p>