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ABC transporter: ATP-binding cassette transporter, important in AMP sensing and/or detoxification.

Abu-S-Ala: methyl lanthionines (cf. Ala-S-Ala, lanthionines)

AD: Atopic Dermatitis or /Eczema (AE), a diseased condition where expression of AMPs such as hCAP-18/LL-37 is suppressed.

AFM: Atomic Force Microscopy

Alarmins: structurally distinct peptide mediators that can recruit and activate antigen-presenting cells (APCs), thereby enhancing immune response. See also DAMP.

Amino acids : A, Ala, alanine; C, Cys, cysteine; D, Asp, asparate; E, Glu, glutamate; F, Phe, phenylallanine; G, Gly, glycine; H, His, histidine; I, Ile, isoleucine; K, Lys,lysine; L, Leu, leucine; M, Met, methionine; N, Asn, asparagine; P, Pro, proline; Q, Gln, glutamine; R, Arg, arginine; S, Ser, serine; T, Thr, threonine; V, Val, valine; W, Trp, tryptophan; and Y, Tyr, tyrosine. SEE ALSO Non-standard AA below.

AMPs : antimicrobial peptides

AKT: v-akt murine thymoma viral oncogene homolog 1

AP-1: Activated Protein-1, a transcription factor

APC: Antigen Presenting Cell

APD : The Antimicrobial Peptide Database, or the AMP database

API: Active Pharmaceutical Ingredient

Archaeocins : Proteinaceous antimicrobials from the domain archaea

ATCC: American Type Culture Collection, founded in 1925, is a repository for donated bacterial strains.

Bacteriocins: Proteinaceous antimicrobials from the domain bacteria. For Gram-positive bacteria, class I bacteriocins are lantibiotics whose polypeptide chains are subject to extensive chemical modifications after translation. Type A has an elongated structure while type B has a more rigid and globular structure. Class II bacteriocins possess unmodified polypeptide chains. This class is further divided into class IIa (the pediocin-like bacteriocins), class IIb (the two-peptide chain bacteriocins, class IIc (cyclic peptides), and class IId (the leaderless peptide bacteriocins). Classes III are large proteins with lytic activity (Cotter P et al., 2005 Nature Rev Microbiol 3: 777). Bacteriocins from Gram-negative bacteria are called microcins (Class I < 5 kDa; Class II, 5-10 kDa; and class III(colicins) > 10 kDa (Duquesne et al. 2007 Nat. Prod. Rep. 24: 708-734).

BB codes for peptide binding partners : BBB, peptide self association; BBII, metal ions; BBL, LPS; BBMm, membranes; BBN, nucleic acids; BBPP, protein/enzyme; BBS, sugars. AMPs with such activities can be searched in the name field of the search interface of the APD by entering the code.

BLP: Bacterial LipoProtein, TLR2/1 ligand (agonist). This BLP binding to TLR2/1 upregulates the expression of vitamin D receptor and the vitamin D-1-hydroxylase genes, leading to the induction of human cathelicidin LL-37 to kill Mycobacterium tuberculosis.

Boman Index : Originally called protein-binding potential by Hans Boman. It was renamed as Boman Index when it was introduced into the APD in 2003. Boman index is the sum of the free energies of the respective side chains for transfer from cyclohexane to water taken from Radzeka and Wolfenden and divided by the total number of the residues of an antimicrobial peptide. The calculated values are negative ( except for the hybrid peptide), but the + and - are reversed [Boman, H.G.(2003)J.Inter.Med.254:197-215].

CAPA: Corrective Action, Preventative Action (FDA)

Cathelicidin: a family of antimicrobial peptides that share the common N-terminal cathelin domain in their precursor proteins

CD: Circular Dichroism, especially good at estimating helix formation with the change in conditions.

CDC: US Centers for Disease Control

CF: Cystic Fibrosis

CFU: Colony-Forming Unit

Colicins : see microcins.

ChIP: Chromatin ImmunoPrecipitation assays

CMC: Critical Micelle Concentration

Core peptide: in the lantipeptide case, it refers to the C-terminal region of the precursor that becomes the final AMP after processing . In other cases, it is also used to refer to the critical AMP region that retains antimicrobial activity.

CpG-ODN: CpG-OligoDeoxyNucleotides (DNA), unmethylated, TLR9 ligand

CQAs: Critical Qaulity Attributes such as viscosity, pH, density, or content uniformity

CNS: Central nervous System

CRE: Carbapenem-resistant Enterobacteriaceae, the "Nightmare bacteria" (CDC director Tom Frieden) detected in over 200 USA hospitals in 2012.

Crohn's disease: a chronic inflammatory bowel disease due to a defect in intestinal innate immune responses to bacteria

CT: Computed Tomography

CTD: Common Technical Document

Cyclotides: Plant circular peptides that have no exposed N- or C-terminal residues.

25D: 25-hydroxyvitamin D3, the major circulating form. Once converted to 1,25D, it can induce LL-37 expression in human cells.

1,25D: 1,25-dihydroxylvitamin D3, the active form of vitamin D that induces the expression of LL-37, hBD-2, and intracellular pattern recognition receptor called NOD2/CARD15 in humans.

DAMP: damage-associated molecular patterns. Examples are alarmins (defensins, cathelicidins, high-mobility group box-1 protein (HMGB1), and iron-binding proteins) and mitochondrial DNA of eukaryotic cells.

DCs: Dendritic Cells

Dha: 2,3-didehydroalanine, dehydrated serine (Ser), or occasionally Cys (Claesen and Bibb 2010 PNAS 107:16297)

Dhb: (Z)-2,3-didehydrobutyrine, dehydrated threonine (Thr)

dpi: (immunology) days post-infection

Drug compounding: a little-known practice in which pharmacists traditionally alter or recombine drugs to meet the special needs of specific patients, e.g. HIV-1 cocktail therapy

DSC: Differential Scanning Calorimetry

eDNA: extracellullar DNA, i.e. genomic DNA released by bacteria, an important component involved in the formation of bacterial biofilms.

EST: Expressed Sequence Tag

EGFR: Epidermal Growth Factor Receptor

ER: Endoplasmic Reticulum

ESKAPE pathogens: the abbreviation of the six multi-drug resistant bacteria, including Enterococcus faecium, Staphylococcus aureus, Klebsiella species, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species.

Eucaryocins : Proteinaceous antimicrobials from the domain eucarya

FACS: Fluorescence-Activated Cell Sorter

FDA: US Food and Drug Administration

Firmicutes: the low-G+C-content gram-positive bacterial species, e.g. bacilli & clostridia.

FITC: Fluorescein isothiocyanate, a flurescent probe widely used in tracing the location of antimicrobial peptides in cells.

FPRL1: Formyl Peptide Receptor-Like 1. Human Ll-37 chemoattracts human neutrophils, monocytes, T cells and multipotent mesenchymal stromal cells (stem cells) by binding to this cell surface receptor. This molecular process could be essential for cancer metastasis (see the minireview on the relationship between LL-37 and cancer, Wu W.K.K. et al. 2010 Int J cancer 127:1741-7).

FRET: Fluorescence Resonance Energy Transfer

FT-IR: Fourier Transform InfraRed spectroscopy

GCP: Good Clinical Practice (FDA)

GLP: Good Laboratory Practice (FDA)

Glycopeptides: glycolated peptides with antimicrobial activity (newly discovered from bacteria in 2011). These are regarded as examples for the class IV peptide (conjugated peptides) originally proposed by Klaenhammer (1993).

GMP: Good Manufacturing Practice (FDA)

GRAS: Generally Recognized As Safe

hBD: human Beta Defensin (28 genes in humans, most common are HBD-1, HBD-2, HBD-3, and HBD-4)

hCAP-18: human Cationic Antimicrobial Protein of 18 kDa (i.e., the precursor of human cathelicidins LL-37 and ALL-38, the mature antimicrobial peptides; originally thought FALL-39). The gene that encodes this protein is referred to as CAMP.

HDP: see "Host Defense Peptide"

HIV-1: Human immunodeficiency Virus type 1

HNP: Human Neutrophil Protein, HNP-1 to HNP-4 made in granulocytes, and human defensins 5 and 6 (HD-5 and HD-6) made in Paneth cells.

Host Defense Peptide: An alternative name for antimicrobial peptides that emphasizes the immune modulation activities of AMPs.

HSP: Heat Shock Proteins, proposed targets for Pro-rich AMPs

HSV: Herpes Simplex Virus.

IACUC: Institutional Animal Care and Use Committee.

IAV: Influenza A Virus that causes seasonal Flu.

IBC: Institutional Biosafety Committee.

IC50: 50% the maximum Inhibition Concentration

IDR: Innate Defence Regulator, which may not kill bacteria directly.

IKK: Inhibitor of Kappa light polypeptide gene enhancer in B-cells, signaling molecules

IL: InterLeukin

IMD: another major pathway in Drosophila that regulates the expression of antimicrobial peptides. The imd pathway is induced primarily by Gram-negative bacteria, while the TOLL pathway is induced by Gram-postive bacteria and fungi.

IND: Investigational New Drug (FDA)

INF: interferon

iNOS: inducible Nitric Oxide Synthase

IRAK: Interleukin-1 Receptor Associated Kinase

IRF3: Interferon Regulatory Factor 3, a transcription factor (activated by phosphorylation)

ITC: Isothermal Titration Calorimetry

Kinocidins: Chemokines with antimicrobial activity. On the other side of the coin, some antimicrobial peptides such as human LL-37 and HBD-3 are now demonstrated to have chemotactic activity. Search the APD for more.

LAB: Lactic Acid Bacteria that produce lantibiotics useful for food preservation.

LAM: LipoArabinoMannan, a glycolipid associated with the cell wall of Mycobacterium tubercolosis

Lan: meso-lanthionine

LanA: the peptide precursor to be processed by lantipeptide modification enzymes

Lantibiotics: lanthionine containing antibiotics which are extensively modified post-translationally.

Lantipeptides: lanthionine containing natural peptides with or without antimicrobial activity.

LBP: LPS-Binding Protein, its complex with LPS binds to CD14 high-affinity LPS receptor on the cell surface and induces cellular response via TLR4, the first mammalian homolog of Drosophila Toll. AMPs such as human LL-37 could compete with LBP, thereby suppressing, at least partially, the lethal effect of LPS-induced immune reponses. The synergistic binding of LPS to human LL-37 may be understood from the two hydrophobic domains due to the existence of Ser9 on the hydrophobic surface of the long amphipathic helix (Wang et al. 2012 Biochemistry 51:653-664). Abstract.

LC50: (50%) Median Lethal Concentration

LC-MS: Liquid Chromatography-Mass Spectrometry

Leader peptide: in the case of lantibiotics, it refers to the N-terminal region of the precursor important for production but unmodified and removed after processing

Lipids: PC, diacyl phosphatidylcholines; PG, diacyl phosphatidylglycerols; PE, diacyl phosphatidylethanolamine

LL-37: a human innate defense peptide with 37 residues and starting with a pair of leucines. This peptide appears to have multiple functions ranging from antimicrobial, chemotactic, and wound healing, to immune modulation.

LPS: LipoPolySaccharides. Also called endotoxin from Gram-negative bacteria. A ligand for TLR4

LRR: Leucine-Rich Repeats

LTA: LipoTeichoic Acid from Gram-positive bacteria

LTP: Lipid Transfer Protein

LUV: Large unilamellar vesicles. e.g. DOPG=1,2-dioleoyl-sn-glycero-3-phosphocholine

MALP-2: Macrophage Activating LipoPeptide-2

MAPK: Mitogen Activated Protein Kinase

MBC: Minimum Bactericidal Concentration

MCP-1: Monocyte Chemotactic Protein-1 (a marker cytokine the level of which is used as an indicator of immune modulation activity of AMPs)

MeLan: (2S,3S,6R)-3-methyllanthionine

MIC: (bacterial) Minimal Inhibitory Concentration

Microcins : Gene-encoded antibacterial peptides (<10 kDa) produced by enterobacteria to inhibit the growth of closely related species. Note that polypeptides (>10 kDa) are called colicins

Membrane-mimetic models: organic solvents such as TFE (trifluoroethanol), detergent micelles such as SDS (sodium dodecylsulfate) or DPC (dodecylphosphocholine), lipid micelles e.g. D8PG (dioctanoyl phosphatidylglycerol), bicelles, and lipid bilayers

MERS: Middle East Respiratory Syndrome, which belongs to the coronavirus family that includes the common cold and SARS, or severe acute respiratory syndrome that caused 800 deaths in 2003.

MOA: Mechanism Of Action

MOI: Multiplicity Of Infection

MRI: Magnetic Resonance Imaging (Nobel Prize in 2003)

MRSA: Methicillin-Resistant Staphylococcus aureus, a difficult-to-kill superbug

MSR: the Macrophage Scavenger Receptor

MTD: the Maximal Tolerance Dose (e.g. 20 mg/kg)

MyD88: Myeloid Differentiation factor 88, a key adaptor protein in the TLR signaling pathways

NDA: New Drug Application

NFkB: Nuclear Factor kappa B, a transcription factor frequently involved in stress response of cells

NHBE cells: Normal Human Bronchial Epithelial cells

NLRs: Nod-like receptors

NMR: Nuclear Magnetic Resonance spectroscopy. While solution NMR is the major technique for structural and dynamics studies of membrane-bound AMPs, solid-state NMR provides complementary information such as peptide oligomerization and orientation in the membranes. (Nobel Prizes in 1952, 1991 and 2002)

NO: Nitric Oxide

NOD: nucleotide-binding oligomerization domain, an intracellular receptor responding to LPS

Non-standard amino-acids : Aad, 3-Aminoadipic acid; Abu, 2-Aminobutyric acid; Aib, aminoisobutyric acid; Apm, 3-Aminopimelic acid; Dab, 2,4-diaminobutyric acid; Dap, 2,3-diaminopropionic acid; Hcy, homocysteine; Hse, Homoserine; Hyl, Hydroxylysine; Hyp, Hydroxyproline; aIle, allo-Isoleucine; MeGly, N-methylglycine; NLys, N-(4-aminonutyl) glycine (a peptoid analog of lysine); Nva, Norvaline; Nle, Norleucine; Orn, Ornithine; Pyr, Pyroglutamic acid; Sar, Sarcosine.

OAK: Oligomers of Acylated Lysines (K)

ORF: Open Reading Frame

Orthologs: genes or gene-coded proteins in different species that evolved from a common ancestral gene, usually with the same function.

PAMPs: Pathogen Associated Molecular Patterns

Paralogs: genes or gene-coded proteins generated by gene duplication within a genome, usually evolving new functions.

PBMC: Peripheral Blood Mononuclear Cells

PBS: Phosphate Buffered Saline

P/C properties: physio-chemical properties

PCR: Polymerase Chain Reaction

PD: Pharmacodynamics

pDCs: plasmacytoid Dendritic Cells

Peptaibol: fungi-derived short-length peptides (Pept ~15-20) rich in nonstandard amino acid residues such as aminoisobutyric acid (Aib) usually with a C-terminal hydroxyl group (OH).

Peptoids: poly N-substituted glycines, e.g. NLys and NHis

PGN: PeptidoGlycaN, TLR2 ligand

PGRP: PeptidoGlycan Recognition Protein

PK: pharmacokinetics

PMN: PolyMorphonuclear Neutrophils

PRR: Pattern Recognition Receptors

PTMs: posttranslational modifications

QSAR: Quantitative Structure-Activity Relationship

QTPP: Quality Target Product Profile

RACE: Rapid Amplification of cDNA Ends. This technique produces cDNA from mRNA via reverse transcription, usually followed by PCR amplification.

RANA box: a C-terminal domain connected by a pair of cysteins discovered in amphibian AMPs.

RAR: Retinoic Acid Receptor

ROS: Reactive Oxygen Species

RP-HPLC: Reversed-Phase High-Performance Liquid Chromatography

RSV: Respiratory Syncytial Virus that can cause acute lower respiratory tract infection in young children worldwide.

SARS: severe acute respiratory syndrome

SAXS: Small-Angle X-ray Scattering

SCVs: Small colony variants, a more resistant form of bacteria. For example, S. aureus can form SCVs in CF patients. This form is shown to be more resistant to cationic AMPs as well (Gläser R et al., 2014).

Sepsis or septicemia: a systemic inflamatory response syndrome in response to pathogenic bacteria or their components in the blood or tissues

SINE: Short Interspersed Element, or a repetitive DNA element (so called "junk DNA"). Note that such a vitamin D receptor binding element exists only in primate and human genomes.

siRNA: small interfering RNA

SNP: Single Nucleotide Polymorphism

SPR: Surface Plasmon Resonance

ssRNA: single-stranded RiboNucleic Acid, TLR7 ligand

STAT: the Signal Transducer and Activator of Transcription protein

Structure classification of antimicrobial peptides: alpha (peptides with alpha-helical structures); beta (AMPs with beta-sheet structure); alphabeta (AMPs with both alpha and beta structures; and non-AlphaBeta (AMPs that contain neither alpha nor beta structures) (Wang, G. 2010 Structural studies of AMPs. In Chapter 1, <"Antimicrobial Peptides: Discovery, Design and Novel Therapeutic Strategies" (edited by G. Wang). Read Chapter 1 here.

TB: tuberculosis

TCR: T Cell Receptor

TCRS: Two-component regulatory system

TEM: Transmission Electron Microscopy

Th1: T helper 1

TIR: Toll/Interleukin-1 Receptor domain

TIRAP: Toll-Interleukin 1 Receptor (TIR) domain containing Adaptor Protein; also known as MyD88-adaptor-like protein or Mal

TLRs: Toll-Like Receptors; sensors of both innate and adaptive immune systems for microbial products; 11 in humans. e.g. TLR2 for lipoteichoic acid from Gram-positive bacteria; TLR4 for LPS from Gram-negative bacteria. However, TLR3, TLR7, TLR8, and TLR9 are endosomal Toll-like receptors.

TNF-alpha: Tumor Necrosis Factor alpha, a cytokine. Some AMPs such as human LL-37 can suppress the release of TNF-alpha (part of the immune modulation activity)

TOCL: TetraOleoleoyl-CardioLipin


Tollip: Toll-interacting protein

TRAF: TNF Receptor-Associated Factor

TRAIL: TNF-Related Apoptosis Inducing Ligand

TRAM: Toll-like Receptor Adaptor Molecule 2

Tregs: regulatory T cells

UPLC: Ultra Performance Liquid Chromatography

UTR: UnTranslated Regions

UVB: solar UltraViolet-B

VDR: Vitamin D Receptor

VDRE: Vitamin D Receptor binding Element

VISA: vancomycin intermediate S. aureus strains, which increase basal resistance to vancomycin withour acqusition of any clearly defined resistance determinants.

VRE: Vancomycin-Resistant Enterococcus or Vancomycin-Resistant Enterococci

XX codes for chemical modification: XXA, C-terminal NH2; XXC, cyclization; XXD, D-amino acids; XXG, glycosylation; XXO, oxidation; XXP, peptide phopsphorylation. AMPs with such activities can be searched in the name field of the search interface of the APD by entering the code.

ZZ codes: ZZH, anti-HIV; ZZP, anti-parasital; ZZS, spermicidal; ZZI, insecticidal. AMPs with such activities can be searched in the name field of the search interface of the APD by entering the code. Since the end of 2011, the ZZ codes have been replaced by more convenient icon search in the same manner as other activity functions created originally in the database.

Last updated: September 2014 | Copyright 2003-2014 Dept of Pathology & Microbiology, UNMC All Rights Reserved