Modeling and simulation of the immune system as a self-regulating network.

Abstract:

:Numerous aspects of the immune system operate on the basis of complex regulatory networks that are amenable to mathematical and computational modeling. Several modeling frameworks have recently been applied to simulating the immune system, including systems of ordinary differential equations, delay differential equations, partial differential equations, agent-based models, and stochastic differential equations. In this chapter, we summarize several recent examples of work that has been done in immune modeling and discuss two specific examples of models based on DDEs that can be used to understand the dynamics of T cell regulation.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Kim PS,Levy D,Lee PP

doi

10.1016/S0076-6879(09)67004-X

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

79-109

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(09)67004-X

journal_volume

467

pub_type

杂志文章
  • Methods for Expression, Purification, and Characterization of PqqE, a Radical SAM Enzyme in the PQQ Biosynthetic Pathway.

    abstract::PqqE is the first enzyme in the biosynthetic pathway of the redox cofactor pyrroloquinoline quinone (PQQ), catalyzing the formation of a carbon-carbon bond in the precursor peptide PqqA. PqqE is a radical S-adenosyl-l-methionine (SAM) (RS) enzyme, a family of enzymes that use the reductive cleavage of a [4Fe-4S] clust...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2018.04.002

    authors: Zhu W,Martins AM,Klinman JP

    更新日期:2018-01-01 00:00:00

  • Chapter 9 the duffy antigen receptor for chemokines.

    abstract::The Duffy blood group antigen is a serpentine protein with seven transmembrane domains that is not coupled to G-proteins or other known intracellular effectors. In addition to erythrocytes, it is also expressed in endothelial cells and neurons. In recent years the Duffy antigen has received much attention because of i...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(09)05409-3

    authors: Rot A,Horuk R

    更新日期:2009-01-01 00:00:00

  • Quantitative Analysis of Yeast Checkpoint Protein Kinase Activity by Combined Mass Spectrometry Enzyme Assays.

    abstract::Virtually all eukaryotic cell functions and signaling pathways are regulated by protein phosphorylation. The Rad53 kinase plays crucial roles in the DNA damage response in Saccharomyces cerevisiae and is widely used as a surrogate marker for DNA damage checkpoint activation by diverse genotoxic agents. Most currently ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.09.032

    authors: Hoch NC,Chen ES,Tsai MD,Heierhorst J

    更新日期:2017-01-01 00:00:00

  • Use of mouse models to study plasminogen activator inhibitor-1.

    abstract::Plasminogen activator inhibitor-1 (PAI-1) is the main inhibitor of tissue-type plasminogen activator (t-PA) and urokinase-type plasminogen activator (u-PA) and therefore plays an important role in the plasminogen/plasmin system. PAI-1 is involved in a variety of cardiovascular diseases (mainly through inhibition of t-...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-386471-0.00005-5

    authors: Declerck PJ,Gils A,De Taeye B

    更新日期:2011-01-01 00:00:00

  • Neural stem cells and their manipulation.

    abstract::Extracellular signals dictate the biological processes of neural stem cells (NSCs) both in vivo and in vitro. The intracellular response elicited by these signals is dependent on the context in which the signal is received, which in turn is decided by previous and concurrent signals impinging on the cell. A synthesis ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(06)19002-3

    authors: Rajan P,Snyder E

    更新日期:2006-01-01 00:00:00

  • QM/MM Analysis of Transition States and Transition State Analogues in Metalloenzymes.

    abstract::Enzymology is approaching an era where many problems can benefit from computational studies. While ample challenges remain in quantitatively predicting behavior for many enzyme systems, the insights that often come from computations are an important asset for the enzymology community. Here we provide a primer for enzy...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.05.016

    authors: Roston D,Cui Q

    更新日期:2016-01-01 00:00:00

  • Characterization of EHT 1864, a novel small molecule inhibitor of Rac family small GTPases.

    abstract::There is now considerable experimental evidence that aberrant activation of Rho family small GTPases promotes uncontrolled proliferation, invasion, and metastatic properties of human cancer cells. Therefore, there is considerable interest in the development of small molecule inhibitors of Rho GTPase function. However,...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(07)00409-0

    authors: Onesto C,Shutes A,Picard V,Schweighoffer F,Der CJ

    更新日期:2008-01-01 00:00:00

  • Preparation of samples for comparative studies of arthropod chromosomes: visualization, in situ hybridization, and genome size estimation.

    abstract::The ability to obtain large amounts of genomic sequence for organisms and high throughput technology has led to a change in the thrust of research at the level of chromosomes in animals. In the past chromosomal analysis of animals was focused on gross changes such as inversions, translocations, and deletions for both ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)95025-8

    authors: DeSalle R,Gregory TR,Johnston JS

    更新日期:2005-01-01 00:00:00

  • Purification of Functional CB1 and Analysis by Site-Directed Fluorescence Labeling Methods.

    abstract::The human cannabinoid receptor, CB1, has been difficult to purify in a functional form, hampering structural and biophysical studies. Here, we present our approaches for obtaining pure, detergent solubilized, functional CB1. We also discuss our site-directed fluorescence labeling (SDFL) methods for identifying differe...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2017.06.026

    authors: Fay JF,Farrens DL

    更新日期:2017-01-01 00:00:00

  • Catalytic pathway of manganese superoxide dismutase by direct observation of superoxide.

    abstract::Measurement of catalysis by MnSOD using direct observation of the UV absorbance of superoxide allows determination of steady-state catalytic constants. Stabilizing superoxide in aprotic solvents such as dimethyl sulfoxide permits the use of stopped-flow spectrophotometry, although significant information is lost in th...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/s0076-6879(02)49321-4

    authors: Silverman DN,Nick HS

    更新日期:2002-01-01 00:00:00

  • Using tandem mass spectrometry to quantify site-specific chlorination and nitration of proteins: model system studies with high-density lipoprotein oxidized by myeloperoxidase.

    abstract::Protein oxidation is implicated in atherogenesis and other inflammatory conditions. Measuring levels of chlorinated and nitrated proteins in biological matrices serves as a quantitative index of oxidative stress in vivo. One potential mechanism for oxidative stress involves myeloperoxidase, a heme protein expressed by...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(07)00803-8

    authors: Shao B,Heinecke JW

    更新日期:2008-01-01 00:00:00

  • Methods to Assess Autophagy and Chronological Aging in Yeast.

    abstract::Autophagy is a catabolic process that is crucial for cellular homeostasis and adaptive response to changing environments. Importantly, autophagy has been shown to be induced in many longevity-associated scenarios and to be required to maintain lifespan extension. Notably, autophagy is a highly conserved cellular proce...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.09.086

    authors: Kainz K,Tadic J,Zimmermann A,Pendl T,Carmona-Gutierrez D,Ruckenstuhl C,Eisenberg T,Madeo F

    更新日期:2017-01-01 00:00:00

  • Analysis and expression of Rab38 in oculocutaneous lung disease.

    abstract::Rab38 is a low-molecular-weight G-protein highly expressed in melanocytes of the skin and alveolar type II cells in the lung. A point mutation in the postulated GTP/GDP-interacting domain of Rab38 has been identified as the genetic lesion responsible for oculocutaneous albinism (OCA) in chocolate (cht) mice. Another p...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(07)38014-2

    authors: Osanai K,Voelker DR

    更新日期:2008-01-01 00:00:00

  • Receptor-driven identification of novel human A₃ adenosine receptor antagonists as potential therapeutic agents.

    abstract::The field of therapeutic application of the A₃ adenosine receptor (A₃AR) antagonists represents a rapidly growing and intense area of research in the adenosine field. Even if there are currently no A₃AR antagonists in clinical phases, in light of the plethora of biological effects attributed to A₃ARs, substantial effo...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-381296-4.00013-0

    authors: Paoletta S,Federico S,Spalluto G,Moro S

    更新日期:2010-01-01 00:00:00

  • Human dicer: purification, properties, and interaction with PAZ PIWI domain proteins.

    abstract::Dicer is a multidomain ribonuclease that processes double-stranded RNAs (dsRNAs) to 21-nt small interfering RNAs (siRNAs) during RNA interference and excises microRNAs (miRNAs) from precursor hairpins. PAZ and PIWI domain (PPD) proteins, also involved in RNAi and miRNA function, are the best-characterized proteins kno...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(04)92019-8

    authors: Kolb FA,Zhang H,Jaronczyk K,Tahbaz N,Hobman TC,Filipowicz W

    更新日期:2005-01-01 00:00:00

  • Measuring isotope fractionation by autotrophic microorganisms and enzymes.

    abstract::Physical, chemical, and biological processes commonly discriminate among stable isotopes. Therefore, the stable isotope compositions of biomass, growth substrates, and products often carry the isotopic fingerprints of the processes that shape them. Therefore, measuring isotope fractionation by enzymes and cultures of ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-385112-3.00014-7

    authors: Scott KM,Fox G,Girguis PR

    更新日期:2011-01-01 00:00:00

  • Imaging single mRNA molecules in yeast.

    abstract::Yeast cells in an isogenic population do not all display the same phenotypes. To study such variation within a population of cells, we need to perform measurements on each individual cell instead of measurements that average out the behavior of a cell over the entire population. Here, we provide the basic concepts and...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(10)70017-3

    authors: Youk H,Raj A,van Oudenaarden A

    更新日期:2010-01-01 00:00:00

  • Site-directed labeling of β-arrestin with monobromobimane for measuring their interaction with G protein-coupled receptors.

    abstract::β-arrestins (βarrs) are multifunctional proteins that interact with activated and phosphorylated G protein-coupled receptors (GPCRs) to regulate their signaling and trafficking. Understanding the intricate details of GPCR-βarr interaction continues to be a key research area in the field of GPCR biology. Bimane fluores...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2019.11.009

    authors: Srivastava A,Baidya M,Dwivedi-Agnihotri H,Shukla AK

    更新日期:2020-01-01 00:00:00

  • Automation in single-particle electron microscopy connecting the pieces.

    abstract::Throughout the history of single-particle electron microscopy (EM), automated technologies have seen varying degrees of emphasis and development, usually depending upon the contemporary demands of the field. We are currently faced with increasingly sophisticated devices for specimen preparation, vast increases in the ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(10)83015-0

    authors: Lyumkis D,Moeller A,Cheng A,Herold A,Hou E,Irving C,Jacovetty EL,Lau PW,Mulder AM,Pulokas J,Quispe JD,Voss NR,Potter CS,Carragher B

    更新日期:2010-01-01 00:00:00

  • De novo design and construction of an inducible gene expression system in mammalian cells.

    abstract::Inducible expression systems represent the founding technology for the emergence of synthetic biology in mammalian cells. The core molecules in these systems are bacterial regulator proteins that bind to or dissociate from a cognate DNA operator sequence in response to an exogenous stimulus like a small-molecule induc...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-385075-1.00011-1

    authors: Karlsson M,Weber W,Fussenegger M

    更新日期:2011-01-01 00:00:00

  • Gene knockouts, in vivo site-directed mutagenesis and other modifications using the delitto perfetto system in Saccharomyces cerevisiae.

    abstract::Gene manipulation serves the purpose of providing a better understanding of the function of specific genes as well as for developing novel variants of the genes of interest. The generation of knockout genes, the alteration, depletion, or enhancement of a particular gene function through the generation of specific gene...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-420067-8.00008-8

    authors: Stuckey S,Storici F

    更新日期:2013-01-01 00:00:00

  • Methods for studying adaptation to the DNA damage checkpoint in yeast.

    abstract::When yeast are faced with irreparable DNA damage, they will first arrest in G2/M, via the DNA damage checkpoint pathway, but will subsequently adapt to that arrest and resume division. Here, we summarize assays that we have used to examine checkpoint adaptation. Specifically, we discuss the merits of inducing DNA dama...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)09009-9

    authors: Toczyski DP

    更新日期:2006-01-01 00:00:00

  • Oxidative DNA glycosylases: recipes from cloning to characterization.

    abstract::As new organisms are being sequenced on a daily basis, new DNA glycosylases that recognize DNA damage can be easily identified in an effort to understand both their phylogenetics and substrate specificities. As a practical matter, existing bacterial and human homologs need to be readily available as laboratory reagent...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(06)08002-5

    authors: Bandaru V,Blaisdell JO,Wallace SS

    更新日期:2006-01-01 00:00:00

  • Analysis of interactions between intraflagellar transport proteins.

    abstract::Intraflagellar transport (IFT) involves the movement of large proteinaceous particles or trains along the length of ciliary and flagellar axonemal microtubules. The particles contain multiple copies of two protein complexes. As isolated from the flagellated model organism, Chlamydomonas reinhardtii, IFT A contains 6 d...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-397945-2.00010-X

    authors: Behal RH,Cole DG

    更新日期:2013-01-01 00:00:00

  • Changing paradigms in thiology from antioxidant defense toward redox regulation.

    abstract::The history of free radical biochemistry is briefly reviewed in respect to major trend shifts from the focus on radiation damage toward enzymology of radical production and removal and ultimately the role of radicals, hydroperoxides, and related fast reacting compounds in metabolic regulation. Selected aspects of the ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(10)73001-9

    authors: Flohé L

    更新日期:2010-01-01 00:00:00

  • Induction and measurement of UPR and osmotic stress in the yeast Pichia pastoris.

    abstract::Unfolded protein response (UPR) is a major reaction to intrinsic stress of eukaryotic organisms and is also related to environmental stress reactions. Among yeasts, stress regulation has mainly been investigated in Saccharomyces cerevisiae, while other species with biotechnological or medical interest are less well un...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-385116-1.00010-8

    authors: Dragosits M,Mattanovich D,Gasser B

    更新日期:2011-01-01 00:00:00

  • Comparative Biochemistry and In Vitro Pathway Reconstruction as Powerful Partners in Studies of Metabolic Diversity.

    abstract::There are estimated to be >300,000 plant species, producing >200,000 metabolites. Many of these metabolites are restricted to specific plant lineages and are referred to as "specialized" metabolites. These serve varied functions in plants including defense against biotic and abiotic stresses, plant-plant and plant-mic...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.02.023

    authors: Fan P,Moghe GD,Last RL

    更新日期:2016-01-01 00:00:00

  • Analysis of Nonsense-Mediated mRNA Decay at the Single-Cell Level Using Two Fluorescent Proteins.

    abstract::Nonsense-mediated mRNA decay (NMD) is an evolutionarily conserved mechanism of specific degradation of transcripts with a premature stop codon. NMD eliminates aberrant mRNAs arising from mutations, alternative splicing, and other events in cells. In addition, many normal transcripts undergo NMD. Recent studies demonst...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.02.008

    authors: Gurskaya NG,Pereverzev AP,Staroverov DB,Markina NM,Lukyanov KA

    更新日期:2016-01-01 00:00:00

  • Dynamic assessment of nitration reactions in vivo.

    abstract::Assessment of protein nitration is commonly used as a footprint for the formation of reactive nitrogen species in vivo. However, one of the major disadvantages of measuring nitrotyrosine in proteins is that nitrated proteins are broken down at variable rates, and the resulting free nitrotyrosine is taken up by cells, ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)96015-1

    authors: Mani AR,Moore KP

    更新日期:2005-01-01 00:00:00

  • Genetic dissection of signaling through the Rcs phosphorelay.

    abstract::The Rcs phosphorelay, consisting of a hybrid sensor kinase, a phosphotransferase, and a response regulator, regulates a large number of bacterial functions. These include capsule production, the target originally defined for these regulators, a small regulatory RNA, and a growing list of additional genes, many of unkn...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(07)23016-2

    authors: Majdalani N,Gottesman S

    更新日期:2007-01-01 00:00:00