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Methods in enzymology cumulative subject index
General Description of the Volume: This is the Cumulative Subject Index for Methods in Enzymology Volumes 290-319. It will supplement the Methods in Enzymology Index Volumes 75, 95, 120, 140, 175, 199,299, 265, and 285. In addition to the Subject Index, this volume includes the complete Contents of each volume indexed, and a Contributor's Index. General Description of the Series: The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with more than 300 volumes (all of them still in print), the series contains much material still relevant today--truly an essential publication for researchers in all fields of life sciences.
Outline of volumes 290-300 : Volume 290. Molecular chaperones -- Volume 291. Caged compounds -- Volume 292. ABC transporters : Biochemical, cellular, and molecular aspects -- Section I. Prokaryotic ABC transporters -- Section II. Eukaryotic ABC transporters -- A. Nonmammalian ABC transport systems -- B. Mammalian P-Glycoproteins -- C. Multidrug resistance associated protein -- D. Cystic fibrosis transmembrane conductance regulator -- E. Sulfonylurea receptor -- F. Intracellular ABC transporters -- Volume 293. Ion channels (Part B) -- Section I. Assembly -- Section II. Genetics -- Section III. Electrophysiology -- Section IV. Expression systems -- Section V. Model simulations -- Volume 294. Ion channels (Part C) -- Section I. Physical methods -- Section II. Purification and reconstitution -- Section III. Second messengers and biochemical approaches -- Section IV. Special channels -- Section V. Toxins and other membrane active compounds -- Section VI. Reagent and information sources -- Volume 295. Energetics of biological macromolecules (Part B) -- Volume 296. Neurotransmitter transporters -- Section I. Purification of transporter proteins and cDNAs -- A. Plasma membrane carriers -- B. Vesicular carriers -- Section II. Pharmacological approaches and binding studies -- Section III. Transport assays and kinetic analyses -- Section IV. Biochemical approaches for structure-function analyses -- Section V. Expression systems and molecular genetic approaches -- Section VI. Application of electrophysiological techniques to neurotransmitter carriers -- Section VII. Microdialysis and electrochemical measurements -- Volume 297. Photosynthesis : Molecular biology of energy capture -- Section I. Genetic approaches to dissect complex functions -- Section II. Photosynthetic complexes : Function / Structure -- Section III. Gene expression of photosynthetic components -- Section IV. Biogenesis and adaptation of photosynthetic components -- Section V. Photosynthetic mutants : Construction and biological / biochemical / biophysical analyses -- Volume 298. Molecular motors and the cytoskeleton (Part B) -- Section I. Analysis of actomyosin-related systems -- Section II. Analysis of microtubule-related systems -- Section III. Other cytoskeletal systems -- Section IV. Cell-free and genetic systems -- Section V. Force production assays -- Section VI. General methods -- Volume 299. Oxidants and antioxidants (Part A) -- Section I. Total antioxidant activity -- Section II. Vitamin C -- Section III. Polyphenols and flavonoids -- Section IV. Thiols -- Section V. Vitamin E and coenzyme Q₁₀ -- Section VI. Carotenoids and retinoids -- Volume 300. Oxidants and antioxidants (Part B ) -- Section I. Oxidative damage to lipids, proteins, and nucleic acids -- A. Lipids -- B. Proteins and nucleic acids -- Section II. Assays in cells, body fluids, and tissues -- Section III. Oxidant and redox-sensitive steps in signal transduction and gene expression -- Section IV. Noninvasive methods.
Outline of volumes 301-310 : Volume 301. Nitric oxide (Part C : Biological and antioxidant activities) -- Section I. Biological activity -- Section II. Nitric oxide donors : Nitrosothiols and nitroxyls -- Section III. Peroxynitrite -- Section IV. Oxidant and antioxidant action -- Volume 302. Green fluorescent protein -- Section I. Monitoring of physiological processes -- Section II. Localization of molecules -- Section III. Special uses -- Section IV. Mutants and variants of green fluorescent protein -- Volume 303. cDNA preparation and characterization -- Section I. cDNA preparation -- Section II. Gene identification -- Section III. Patterns of mRNA expression -- Section IV. Functional relationship among cDNA translation products -- Volume 304. Chromatin -- Section I. Assembly of nucleosomes, chromatin, and nuclei -- Section II. Assays for nucleosome structure and function in Vitro -- Section III. Assays for chromatin structure and function in Vivo -- Section IV. Chromatin remodeling complexes -- Volume 305. Bioluminescence and chemiluminescence (Part C) -- Section I. Chemiluminescence and bioluminescence : Overviews -- Section II. Instrumentation -- Section III. Luciferases, luminescence accessory proteins, and substrates -- Section IV. Bacterial autoinduction system and its applications -- Section V. Luminescence-based assays in Vitro -- Section VI. Luminescence monitoring in Vivo -- Section VII. Bioluminescence as an education tool -- Volume 306. Expression of recombinant genes in eukaryotic systems -- Section I. Analysis of gene expression -- Section II. Gene expression systems for functional analysis -- Section III. Yeast expression systems -- Section IV. RNA-based control of recombinant gene expression -- Section V. Small molecule control of recombinant gene expression -- Section VI. Viral systems for recombinant gene expression -- Volume 307. Confocal microscopy -- Section I. Theory and practical considerations -- Section II. General techniques -- Section III. Measurement of subcellular relations and volume determinations -- Section IV. Imaging of processes -- Section V. Imaging of ions -- Section VI. Imaging of specialized tissues -- Section VII. Imaging viruses and fungi -- Volume 308. Enzyme kinetics and mechanism (Part E : Energetics of enzyme catalysis) -- Section I. Energetic coupling in enzymatic reactions -- Section II. Intermediates and complexes in catalysis -- Section III. Detection and properties of low-barrier hydrogen bonds -- Section IV. Transition state determination and inhibitors -- Volume 309. Amyloid, prions, and other protein aggregates -- Section I. Characterization of in Vivo protein deposition -- A. Identification and isolation of aggregates -- B. Isolation and characterization of protein deposit components -- C. Characterization of aggregates in Situ and in Vitro -- Section II. Characterization of in Vitro protein deposition -- A. Managing the aggregation process -- B. Aggregation theory -- C. Monitoring aggregate growth by dye binding -- D. Measurement and characterization of assembly intermediates -- E. Monitoring aggregate growth by measuring solid-phase accumulation -- F. Monitoring aggregate growth and structure using light scattering -- G. Aggregation inhibitors -- Section III. Aggregate and precursor protein structure -- A. Aggregate morphology -- B. Molecular level aggregate structure -- C. Characterization of precursor protein structure -- Section IV. Cellular and organismic consequences of protein deposition -- A. Microbial model systems -- B. Animal models of protein deposition diseases -- C. Cell studies on protein aggregate cytotoxicity -- Volume 310. Biofilms -- Section I. Molecular biology of biofilm bacteria -- Section II. Microscopic methods of biofilm formation and physiology -- Section III. Flow and steady-state methods -- Section IV. Biofilms in archaea -- Section V. Physical methods -- Section VI. Physiology of biofilm-associated microorganisms -- Section VII. Substrate for biofilm development -- Section VIII. Antifouling methods.
Outline of volumes 311-319 : Volume 311. Sphingolipid metabolism and cell signaling (Part A) -- Section I. Sphingolipid metabolism -- A. Biosynthesis -- B. Turnover -- C. Genetic approaches -- Section II. Inhibitors of sphingolipid biosynthesis -- Section III. Chemical and enzymatic synthesis -- Volume 312. Sphingolipid metabolism and cell signaling (Part B) -- Section I. Methods for analyzing sphingolipids -- Section II. Methods for analyzing aspects of sphingolipid metabolism in intact cells -- Section III. Sphingolipid-protein interactions and cellular targets -- Section IV. Sphingolipid transport and trafficking -- Section V. Other methods -- Volume 313. Antisense technology (Part A : General methods, methods of delivery, and RNA studies) -- Section I. General methods -- Section II. Methods of delivery -- Section III. RNA studies -- Volume 314. Antisense technology (Part B : Applications) -- Section I. Antisense receptor targets -- Section II. Antisense neuroscience targets -- Section III. Antisense in nonneuronal tissues -- Section IV. Antisense in therapy -- Volume 315. Vertebrate phototransduction and the visual cycle (Part A) -- Section I. Expression and isolation of opsins -- Section II. Characterization of opsins -- Section III. Proteins that interact with rhodopsin -- Section IV. Transducin and regulators of G-Protein signaling -- Section V. Photoreceptor protein phosphatases -- Section VI. Photoreceptor phosphodiesterase and guanylyl cyclase -- Section VII. Cyclic nucleotide-gated channels -- Section VIII. Na⁺ / Ca²⁺-K⁺ exchanger and ABCR transporter -- Volume 316. Vertebrate phototransduction and the visual cycle (Part B) -- Section I. Photoreceptor proteins -- Section II. Calcium-binding proteins and calcium measurements in photoreceptor cells -- Section III. Phototransduction -- Section IV. Enzymes of the visual cycle -- Section V. Posttranslational and chemical modifications -- Section VI. Analysis of animal models of retinal diseases -- Section VII. Inherited retinal disease : From the defective gene to its function and repair -- Volume 317. RNA-ligand interactions (Part A : Structural biology methods) -- Section I. Semisynthetic methodologies -- A. RNA synthetic methods -- B. Derivatization of RNA -- Section II. RNA structure determination -- A. X-ray crystallography -- B. Nuclear magnetic resonance spectroscopy -- C. Electron microscopy -- Section III. Techniques for monitoring RNA conformation and dynamics -- A. Solution methods -- B. Electrophoretic and spectroscopic methods -- Section IV. Modeling tertiary structure -- Volume 318. RNA-ligand interactions (Part B : Molecular biology methods) -- Section I. Solution probe methods -- Section II. Tethered-probe methodologies -- A. Photochemical reagents -- B. Chemical reagents -- Section III. In Vitro affinity selection methodologies -- Section IV. Genetic methodologies for detecting RNA-protein interactions -- A. Bacterial systems -- B. Eukaryotic systems -- Section V. Protein engineering methodologies useful for RNA-protein interaction studies -- Section VI. Cell biology methods -- Volume 319. Singlet oxygen, UV-A, and ozone -- Section I. Singlet oxygen -- A. Generation and detection : Chemical systems -- B. Generation and detection : Biological systems -- C. Biological effects : Role in signaling -- D. Toxic effects -- E. Protection : Singlet oxygen quenchers -- Section II. Ultraviolet A -- A. Dosimetry -- B. Biological responses : Signaling -- C. Biological responses : Photocarcinogenesis, photoaging, and photoallergic reactions -- D. Oxidative damage markers -- E. Protection -- Section III. Ozone -- Section IV. General methods.
editors in chief, John N. Abelson, Melvin I. Simon.
Founding editors: Sidney P. Colowick and Nathan O. Kaplan.
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