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1.
Anal Bioanal Chem ; 413(21): 5333-5347, 2021 Sep.
Article in English | MEDLINE | ID: mdl-34235566

ABSTRACT

Skin secretion represents the only means of defense for the majority of frog species. That phenomenon is based on the fact that the main components of the secretion are peptides demonstrating greatly varying types of bioactivity. They fulfill regulatory functions, fight microorganisms and may be even helpful against predators. These peptides are considered to be rather promising pharmaceuticals of future generation as according to the present knowledge microorganisms are unlikely to develop resistance to them. Mass spectrometry sequencing of these peptides is the most efficient first step of their study providing reliably their primary structures, i.e., amino acids sequence and S-S bond motif. Besides discovering new bioactive peptides, mass spectrometry appears to be an efficient tool of taxonomy studies, allowing for distinguishing not only between closely related species, but also between populations of the same species. Application of several tandem mass spectrometry tools (CID, HCD, ETD, EThcD) available with Orbitrap mass analyzer allowed us to obtain full sequence of about 60 peptides in the secretion of Slovenian population of brown ranid frog Rana temporaria. The problem of sequence inside C-terminal cycle formed by two Cys and differentiation of isomeric Leu and Ile residues was done in top-down mode without any derivatization steps. Besides general biomarkers of Rana temporaria species, Central Slovenian population of Rana temporaria demonstrates six novel temporins and one brevinin 1, which may be treated as biomarkers of that population.


Subject(s)
Amphibian Proteins/analysis , Antimicrobial Cationic Peptides/analysis , Rana temporaria , Amino Acid Sequence , Animals , Moscow , Rana temporaria/metabolism , Sequence Analysis, Protein , Skin/chemistry , Slovenia , Species Specificity , Tandem Mass Spectrometry
2.
Article in English | MEDLINE | ID: mdl-29980138

ABSTRACT

Peptidomic analysis (reversed-phase HPLC combined with MALDI-TOF mass spectrometry and automated Edman degradation) of norepinephrine-stimulated skin secretions from the Trinidadian leaf frog Phyllomedusa trinitatis Mertens 1926 led to the identification and structural characterization of 26 host-defense peptides. On the basis of amino acid sequence similarity, the peptides may be divided into the followings groups: dermaseptins with the conserved N-terminal region GLWSKIK (6 peptides), dermaseptins with the N-terminal region ALWKXXLK (5 peptides), dermaseptins with the conserved N-terminal region GLFKTLIKGAGKMLGHVAK (4 peptides), C-terminally α-amidated and non-amidated forms of the phylloseptins (9 peptides), phyllocaerulein, a peptide (GLVSGLLNSVTGLLGNLAGGGL) with structural similarity to the plasticins, and a putative antioxidant peptide (LTWKIPTRFCGVT). The primary structures of the peptides support the claim based upon morphological criteria that P. trinitatis and Phyllomedusa tarsius are very closely related phylogenetically but are probably not conspecific. Among the phylloseptins, phylloseptin-1.1TR (FLSLIPKIAGGIASLVKNL.NH2) displayed the most potent antimicrobial activity.


Subject(s)
Amphibian Proteins/analysis , Anti-Infective Agents/analysis , Antimicrobial Cationic Peptides/analysis , Anura/metabolism , Skin/chemistry , Amino Acid Sequence , Amphibian Proteins/metabolism , Amphibian Proteins/pharmacology , Animals , Anti-Infective Agents/metabolism , Anti-Infective Agents/pharmacology , Antimicrobial Cationic Peptides/metabolism , Antimicrobial Cationic Peptides/pharmacology , Bacteria/drug effects , Bacterial Infections/drug therapy , Candida albicans/drug effects , Candidiasis/drug therapy , Conserved Sequence , Female , Humans , Male , Skin/metabolism
3.
Sci Rep ; 7(1): 6647, 2017 07 27.
Article in English | MEDLINE | ID: mdl-28751633

ABSTRACT

Salamanders have developed a wide variety of antipredator mechanisms, including tail autotomy, colour patterns, and noxious skin secretions. As an addition to these tactics, the red-legged salamander (Plethodon shermani) uses adhesive secretions as part of its defensive strategy. The high bonding strength, the fast-curing nature, and the composition of the biobased materials makes salamander adhesives interesting for practical applications in the medical sector. To understand the adhesive secretions of P. shermani, its components were chemically analysed by energy dispersive X-ray spectroscopy (EDX), inductively coupled plasma mass spectrometry (ICP-MS), amino acid analysis, and spectroscopy (ATR-IR, Raman). In addition, proteins were separated by gel-electrophoresis and selected spots were characterised by peptide mass fingerprinting. The salamander secretion contains a high amount of water and predominantly proteins (around 77% in the dry stage). The gel-electrophoresis and peptide mass fingerprint analyses revealed a de novo set of peptides/proteins, largely with a pI between 5.0 and 8.0 and a molecular mass distribution between 10 and 170 kDa. Only low homologies with other proteins present in known databases could be identified. The results indicate that the secretions of the salamander Plethodon clearly differ chemically from those shown for other glue-producing terrestrial or marine species and thus represent a unique glue system.


Subject(s)
Amphibian Proteins/analysis , Bodily Secretions/chemistry , Peptides/analysis , Urodela/metabolism , Adhesives/chemistry , Adhesives/metabolism , Animals , Bodily Secretions/metabolism , Spectrum Analysis
4.
Sci Rep ; 7: 44438, 2017 03 20.
Article in English | MEDLINE | ID: mdl-28317844

ABSTRACT

Worldwide amphibian populations are declining due to habitat loss, disease and pollution. Vulnerability to environmental contaminants such as pesticides will be dependent on the species, the sensitivity of the ontogenic life stage and hence the timing of exposure and the exposure pathway. Herein we investigated the biochemical tissue 'fingerprint' in spawn and early-stage tadpoles of the Common frog, Rana temporaria, using attenuated total reflection-Fourier-transform infrared (ATR-FTIR) spectroscopy with the objective of observing differences in the biochemical constituents of the respective amphibian tissues due to varying water quality in urban and agricultural ponds. Our results demonstrate that levels of stress (marked by biochemical constituents such as glycogen that are involved in compensatory metabolic mechanisms) can be observed in tadpoles present in the pond most impacted by pollution (nutrients and pesticides), but large annual variability masked any inter-site differences in the frog spawn. ATR-FTIR spectroscopy is capable of detecting differences in tadpoles that are present in selected ponds with different levels of environmental perturbation and thus serves as a rapid and cost effective tool in assessing stress-related effects of pollution in a vulnerable class of organism.


Subject(s)
Larva/drug effects , Pesticides/toxicity , Rana temporaria/metabolism , Water Pollutants, Chemical/toxicity , Zygote/drug effects , Amphibian Proteins/analysis , Amphibian Proteins/metabolism , Animals , Glycogen/analysis , Glycogen/biosynthesis , Larva/growth & development , Larva/metabolism , Lipids/analysis , Ponds/chemistry , Rana temporaria/growth & development , Spectroscopy, Fourier Transform Infrared , Water Quality , Zygote/growth & development , Zygote/metabolism
5.
J Exp Biol ; 220(Pt 7): 1210-1221, 2017 04 01.
Article in English | MEDLINE | ID: mdl-28096430

ABSTRACT

In vertebrates, many responses to stress as well as homeostatic maintenance of basal metabolism are regulated by plasma glucocorticoid hormones (GCs). Despite having crucial functions, levels of GCs are typically variable among individuals. We examined the contribution of several physiological factors to individual variation in plasma corticosterone (CORT) and the number of corticotropin-releasing hormone (CRH) neurons in the magnocellular preoptic area of the brain in free-living Allegheny Mountain dusky salamanders. We addressed three hypotheses: the current-condition hypothesis, the facilitation hypothesis and the trade-off hypothesis. Differential white blood cell count was identified as a strong contributor to individual variation in baseline CORT, stress-induced CORT and the number of CRH neurons. In contrast, we found no relationship between CORT (or CRH) and body condition, energy stores or reproductive investment, providing no support for the current-condition hypothesis or the trade-off hypothesis involving reproduction. Because of the difficulties of interpreting the functional consequences of variation in differential white blood cell counts, we were unable to distinguish between the facilitation hypothesis or the trade-off hypothesis related to immune function. However, the strong association between differential white blood cell count and hypothalamic-pituitary-adrenal/interrenal (HPA/I) activation suggests that a more thorough examination of immune profiles is critical to understanding variation in HPA/I activation.


Subject(s)
Corticosterone/blood , Urodela/blood , Amphibian Proteins/analysis , Animals , Corticosterone/metabolism , Corticotropin-Releasing Hormone/analysis , Female , Leukocytes/cytology , Male , Reproduction , Seasons , Stress, Physiological , Urodela/physiology
6.
J Exp Zool A Ecol Genet Physiol ; 325(8): 511-523, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27581888

ABSTRACT

Parotoid glands of amphibians are known for the production of several biologically active compounds having pharmacological and toxic effects in mammals. In the present work, a protein fraction obtained from Rhinella schneideri parotoid gland (RsPP) was characterized to study its biological and toxic effects. Rhinella schneideri parotoid secretion is composed of up to 30% (w/w) of soluble proteins. Tandem mass spectrometric analysis of the RsPP identified 104 proteins, including actin, beta-actin, ribosomal proteins, catalase, galectin, and uncharacterized proteins; however, no peptidases were found, and this result was reinforced by the absence of proteolytic activity. In addition, RsPP did not exhibit pro-coagulant or antibacterial effects. However, pretreatment of mice with different doses of RsPP intraperitoneally inhibited carrageenan-induced paw edema and increased tissue myeloperoxidase activity. RsPP also reduced interleukin 1ß levels in the peritoneal cavities and cell migration in the peritoneal cavities of an animal model of carrageenan-induced peritonitis. Subchronic treatment of animals with RsPP for 7 consecutive days did not alter the serum biochemical, renal, or liver parameters. However, a significant reduction in blood leukocyte count was observed. Our results showed that R. schneideri parotoid secretion contains proteins with anti-inflammatory and slight toxic effects.


Subject(s)
Amphibian Proteins/pharmacology , Amphibian Venoms/pharmacology , Anti-Inflammatory Agents/pharmacology , Edema/drug therapy , Peritonitis/drug therapy , Amphibian Proteins/analysis , Amphibian Proteins/toxicity , Amphibian Venoms/chemistry , Amphibian Venoms/toxicity , Animals , Bufonidae/metabolism , Edema/metabolism , Extremities , Female , Leukocyte Count , Male , Mice , Peroxidase/drug effects , Tandem Mass Spectrometry
7.
J Exp Zool A Ecol Genet Physiol ; 325(7): 425-33, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27460953

ABSTRACT

Some amphibian species have developed a breeding strategy in which they deposit their eggs in stable foam nests to protect their eggs and larvae. The frog foam nests are rich in proteins (ranaspumin), especially surfactant proteins, involved in the production of the foam nest. Despite the ecological importance of the foam nests for evolution and species conservation, the biochemical composition, the long-term stability and even the origin of the components are still not completely understood. Recently we showed that Lv-RSN-1, a 23.5-kDa surfactant protein isolated from the nest of the frog Leptodacylus vastus, presents a structural conformation distinct from any protein structures yet reported. So, in the current study we aimed to reveal the protein composition of the foam nest of L. vastus and further characterize the Lv-RSN-1. Proteomic analysis showed the foam nest contains more than 100 of proteins, and that Lv-RSN-1 comprises 45% of the total proteins, suggesting a key role in the nest construction and stability. We demonstrated by Western blotting that Lv-RSN-1 is mainly produced only by the female in the pars convoluta dilata, which highlights the importance of the female preservation for conservation of species that depend on the production of foam nests in the early stages of development. Overall, our results showed the foam nest of L. vastus is composed of a great diversity of proteins and that besides Lv-RSN-1, the main protein in the foam, other proteins must have a coadjuvant role in building and stability of the nest.


Subject(s)
Amphibian Proteins/chemistry , Anura/metabolism , Cloaca/metabolism , Oviducts/metabolism , Amphibian Proteins/analysis , Amphibian Proteins/isolation & purification , Amphibian Proteins/metabolism , Animals , Anura/physiology , Female , Male , Protein Conformation , Proteomics , Reproduction , Surface-Active Agents/chemistry
8.
Rapid Commun Mass Spectrom ; 30(2): 265-76, 2016 Jan 30.
Article in English | MEDLINE | ID: mdl-27071218

ABSTRACT

RATIONALE: Mass spectrometry has shown itself to be the most efficient tool for the sequencing of peptides. However, de novo sequencing of novel natural peptides is significantly more challenging in comparison with the same procedure applied for the tryptic peptides. To reach the goal in this case it is essential to select the most efficient methods of triggering fragmentation and combine all the possible complementary techniques. METHODS: Collision-induced dissociation (CID), high-energy collision dissociation (HCD), and electron-transfer dissociation (ETD) tandem mass spectra recorded with a LTQ Orbitrap Velos instrument were used for the elucidation of the sequence of the natural non-tryptic peptides from the skin secretion of Rana latastei. Manual interpretation of the spectra was applied. RESULTS: The combined approach using CID, HCD, and ETD tandem mass spectra of the multiprotonated peptides in various charge states, as well as of their proteolytic fragments, allowed the sequences of seven novel peptides from the skin secretion of Rana latastei to be established. CONCLUSIONS: Manual mass spectrometry sequencing of natural non-tryptic peptides from the skin secretion of Rana latastei provided the opportunity to work successfully with these species and demonstrated once again its advantage over automatic approaches.


Subject(s)
Amphibian Proteins/analysis , Ranidae , Sequence Analysis, Protein/methods , Skin/chemistry , Tandem Mass Spectrometry/instrumentation , Tandem Mass Spectrometry/methods , Amino Acid Sequence , Amphibian Proteins/chemistry , Animals , Antimicrobial Cationic Peptides/analysis , Antimicrobial Cationic Peptides/chemistry , Female , Molecular Sequence Data , Peptides/analysis , Peptides/chemistry , Reproducibility of Results
9.
Acta Biol Hung ; 67(1): 121-4, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26960362

ABSTRACT

Here, we report two novel peptides identified from the skin secretion, having homologies to Lividin and Spinulosain, of an endemic frog, Hydrophylax bahuvistara, of Western Ghats. This is the first report of these peptides from Indian frogs and first identification of Lividin from the Hydrophylax genus. Both peptides exhibited weak antimicrobial activity but very low haemolytic activity. The problems of naming amphibian host defense peptides (HDPs) are also discussed.


Subject(s)
Amphibian Proteins/analysis , Antimicrobial Cationic Peptides/analysis , Bodily Secretions/chemistry , Ranidae , Skin/metabolism , Amphibian Proteins/chemistry , Animals , Antimicrobial Cationic Peptides/chemistry , Microbial Sensitivity Tests
10.
Anal Chem ; 86(14): 7017-22, 2014 Jul 15.
Article in English | MEDLINE | ID: mdl-24940639

ABSTRACT

An efficient approach to easy and reliable differentiation between isomeric leucine and isoleucine in peptide sequencing utilizes multistage electron transfer dissociation and higher energy collision activated dissociation in the Orbitrap Fusion mass spectrometer. The MS(3) method involves production and isolation of primary odd-electron z(•) ions, followed by radical site initiation of their fragmentation with formation of w-ions, characteristic of the isomeric amino acid residues. Six natural nontryptic peptides isolated from the secretion of frog Rana ridibunda were studied. Their lengths were in the range between 15 and 37 amino acids and the number of targeted isomeric (Leu/Ile) residues varied between 1 and 7. The experiments were successful in all 22 cases of Leu/Ile residues, leaving no doubts in identification. The method is extremely selective as the targeted w-ions appear to be the most intense in the spectra. The proposed approach may be incorporated into shotgun proteomics algorithms and allows for the development of an exclusively mass spectrometric method for automated complete de novo sequencing of various peptides and proteins.


Subject(s)
Amphibian Proteins/analysis , Isoleucine/analysis , Leucine/analysis , Mass Spectrometry/methods , Sequence Analysis, Protein/instrumentation , Sequence Analysis, Protein/methods , Amino Acid Sequence , Amphibian Proteins/chemistry , Animals , Antimicrobial Cationic Peptides/analysis , Isomerism , Male , Molecular Sequence Data , Rana ridibunda
11.
J Morphol ; 275(1): 51-6, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24127169

ABSTRACT

Apoptosis (programmed cell death) occurs during normal development of anurans in organs such as gills, gut, and tail. For example, apoptotic cells have been reported in the luminal epithelium along the length of the digestive tract of both larvae and frogs; however, timing of the peak number of such cells varies in different species. The purpose of the present study was to ascertain whether apoptosis also varies by species during metamorphic restructuring of the skin (as larval epithelium is replaced by adult epidermis). To determine this, cross-sections of dorsal skin from representative larval stages and frogs of Rana pipiens, R. catesbeiana, and Ceratophrys ornata were incubated with monoclonal antibody against active caspase-3, one of the main enzymes in the apoptotic cascade. We observed apoptotic cells in the epidermis of the skin of the three species and found that such cells were more numerous in larval stages than in frogs and more abundant in the two ranid species than in C. ornata. These results contribute to our understanding of metamorphic changes in anuran skin.


Subject(s)
Anura/physiology , Apoptosis , Epidermal Cells , Rana catesbeiana/physiology , Rana pipiens/physiology , Amphibian Proteins/analysis , Animals , Anura/growth & development , Caspase 3/analysis , Larva/cytology , Larva/growth & development , Larva/physiology , Metamorphosis, Biological , Rana catesbeiana/growth & development , Rana pipiens/growth & development
12.
Cryobiology ; 67(2): 175-83, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23850824

ABSTRACT

In the present work we investigated the seasonal variations of apoptotic and antioxidant proteins in the heart and gastrocnemius muscle of the amphibian Pelophylax ridibundus. Particularly processes studied included the evaluation of hypoxia through the levels of transcriptional factor Hif-1α, of apoptosis through the determination of Bcl-2 and Bax, ubiquitin conjugates levels and the antioxidant defense through the determination of the activity of enzymes such as superoxide dismutase, catalase and glutathione peroxidase. Due to a general metabolic depression during overwintering, levels of the above mentioned proteins and enzymes are generally retained at low levels of expression and activity in the examined tissues of P. ridibundus. On the other hand recovery from overwintering induces oxidative stress, followed by increased levels of the specific proteins and enzymes. A milder up-regulation of antioxidant enzymes during overwintering probably prepares P. ridibundus for oxidative stress during arousal. The seasonal activation of these mechanisms seems to protect this species from these unfavourable conditions.


Subject(s)
Amphibian Proteins/metabolism , Ranidae/metabolism , Amphibian Proteins/analysis , Animals , Antioxidants/metabolism , Apoptosis , Cold Temperature , Muscle, Skeletal/metabolism , Myocardium/metabolism , Oxidative Stress , Seasons
13.
PLoS One ; 8(4): e60818, 2013.
Article in English | MEDLINE | ID: mdl-23585852

ABSTRACT

Antimicrobial peptides (AMPs) isolated from several organisms have been receiving much attention due to some specific features that allow them to interact with, bind to, and disrupt cell membranes. The aim of this paper was to study the interactions between a membrane mimetic and the cationic AMP Ctx(Ile(21))-Ha as well as analogues containing the paramagnetic amino acid 2,2,6,6-tetramethylpiperidine-1-oxyl-4-amino-4-carboxylic acid (TOAC) incorporated at residue positions n = 0, 2, and 13. Circular dichroism studies showed that the peptides, except for [TOAC(13)]Ctx(Ile(21))-Ha, are unstructured in aqueous solution but acquire different amounts of α-helical secondary structure in the presence of trifluorethanol and lysophosphocholine micelles. Fluorescence experiments indicated that all peptides were able to interact with LPC micelles. In addition, Ctx(Ile(21))-Ha and [TOAC(13)]Ctx(Ile(21))-Ha peptides presented similar water accessibility for the Trp residue located near the N-terminal sequence. Electron spin resonance experiments showed two spectral components for [TOAC(0)]Ctx(Ile(21))-Ha, which are most likely due to two membrane-bound peptide conformations. In contrast, TOAC(2) and TOAC(13) derivatives presented a single spectral component corresponding to a strong immobilization of the probe. Thus, our findings allowed the description of the peptide topology in the membrane mimetic, where the N-terminal region is in dynamic equilibrium between an ordered, membrane-bound conformation and a disordered, mobile conformation; position 2 is most likely situated in the lipid polar head group region, and residue 13 is fully inserted into the hydrophobic core of the membrane.


Subject(s)
Amphibian Proteins/chemistry , Antimicrobial Cationic Peptides/chemistry , Cell Membrane/chemistry , Molecular Dynamics Simulation , Amino Acid Sequence , Amphibian Proteins/analysis , Animals , Antimicrobial Cationic Peptides/analysis , Anura/metabolism , Circular Dichroism , Cyclic N-Oxides , Electron Spin Resonance Spectroscopy , Hydrophobic and Hydrophilic Interactions , Lysophosphatidylcholines , Membranes, Artificial , Micelles , Molecular Sequence Data , Protein Structure, Secondary , Spin Labels , Trifluoroethanol
14.
Cell Mol Life Sci ; 70(15): 2773-86, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23503622

ABSTRACT

Pseudomonas aeruginosa is an opportunistic bacterial pathogen that forms sessile communities, named biofilms. The non-motile forms are very difficult to eradicate and are often associated with the establishment of persistent infections, especially in patients with cystic fibrosis. The resistance of P. aeruginosa to conventional antibiotics has become a growing health concern worldwide and has prompted the search for new anti-infective agents with new modes of action. Naturally occurring antimicrobial peptides (AMPs) represent promising future template candidates. Here we report on the potent activity and membrane-perturbing effects of the amphibian AMP esculentin(1-21), on both the free-living and sessile forms of P. aeruginosa, as a possible mechanism for biofilm disruption. Furthermore, the findings that esculentin(1-21) is able to prolong survival of animals in models of sepsis and pulmonary infection indicate that this peptide can be a promising template for the generation of new antibiotic formulations to advance care of infections caused by P. aeruginosa.


Subject(s)
Amphibian Proteins/pharmacology , Antimicrobial Cationic Peptides/pharmacology , Biofilms/drug effects , Pseudomonas Infections/prevention & control , Pseudomonas aeruginosa/drug effects , Amino Acid Sequence , Amphibian Proteins/analysis , Amphibian Proteins/genetics , Antimicrobial Cationic Peptides/analysis , Antimicrobial Cationic Peptides/genetics , Biofilms/growth & development , Chromatography, High Pressure Liquid , Colony Count, Microbial , Microscopy, Electron, Scanning , Molecular Sequence Data , Organic Chemicals , Pseudomonas aeruginosa/ultrastructure , beta-Galactosidase
15.
Hear Res ; 283(1-2): 70-9, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22146424

ABSTRACT

Three species of anuran amphibians (Odorrana tormota, Odorrana livida and Huia cavitympanum) have recently been found to detect ultrasounds. We employed immunohistochemistry and confocal microscopy to examine several morphometrics of the inner ear of these ultrasonically sensitive species. We compared morphological data collected from the ultrasound-detecting species with data from Rana pipiens, a frog with a typical anuran upper cut-off frequency of ∼3 kHz. In addition, we examined the ears of two species of Lao torrent frogs, Odorrana chloronota and Amolops daorum, that live in an acoustic environment approximating those of ultrasonically sensitive frogs. Our results suggest that the three ultrasound-detecting species have converged on small-scale functional modifications of the basilar papilla (BP), the high-frequency hearing organ in the frog inner ear. These modifications include: 1. reduced BP chamber volume, 2. reduced tectorial membrane mass, 3. reduced hair bundle length, and 4. reduced hair cell soma length. While none of these factors on its own could account for the US sensitivity of the inner ears of these species, the combination of these factors appears to extend their hearing bandwidth, and facilitate high-frequency/ultrasound detection. These modifications are also seen in the ears of O. chloronota, suggesting that this species is a candidate for high-frequency hearing sensitivity. These data form the foundation for future functional work probing the physiological bases of ultrasound detection by a non-mammalian ear.


Subject(s)
Ear, Inner/anatomy & histology , Ear, Inner/physiology , Hearing , Rana pipiens/anatomy & histology , Rana pipiens/physiology , Ultrasonics , Actins/analysis , Adaptation, Physiological , Amphibian Proteins/analysis , Animals , Biomarkers/analysis , Ear, Inner/chemistry , Immunohistochemistry , Male , Microscopy, Confocal , Myosin Heavy Chains/analysis , Organ of Corti/anatomy & histology , Organ of Corti/physiology , Species Specificity
16.
J Proteome Res ; 10(9): 4230-40, 2011 Sep 02.
Article in English | MEDLINE | ID: mdl-21740067

ABSTRACT

Tree frogs produce a variety of skin defensive chemicals against many biotic and abiotic risk factors for their everyday survival. By proteomics or peptidomics and coupling transcriptome analysis with pharmacological testings, 27 peptides or proteins belonging to 9 families, which act mainly as defensive functions, were identified and characterized from skin secretions of the tree frog, Hyla simplex. They are: (1) a novel family of peptides with EGF- and VEGF-releasing activities; (2) a novel family of analgesic peptides; (3) a family of neurotoxins acting on sodium channel; (4) a snake venom-like presynaptically active neurotoxin; (5) a snake venom-like neurotoxin targeting cyclic nucleotide-gated ion channels; (6) a tachykinin-like peptide, which is the first report from tree frogs; (7) two antimicrobial peptides; (8) a alpha-1-antitrypsin-like serpin; and (9) a wasp venom-like toxin with serine protease inhibitors activity. Families of 1, 2, 4, 5, and 8 proteins or peptides are first reported in amphibians. The chemical array in the tree frog skin shares some similarities with snake venoms. Most of these components in this tree frog help defend against predators, heal wounds, or attenuate suffering.


Subject(s)
Amphibian Proteins/analysis , Anura/metabolism , Proteomics/methods , Skin/chemistry , Amino Acid Sequence , Amphibian Proteins/chemistry , Amphibian Proteins/pharmacology , Animals , Cloning, Molecular , Microbial Sensitivity Tests , Molecular Sequence Data , Sequence Alignment , Skin/metabolism
17.
Peptides ; 32(7): 1502-8, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21664395

ABSTRACT

Mueller's clawed frog Xenopus muelleri (Peters 1844) occupies two non-contiguous ranges in east and west Africa. The phylogenetic relationship between the two populations is unclear and it has been proposed that the western population represents a separate species. Peptidomic analysis of norepinephrine-stimulated skin secretions from X. muelleri from the eastern range resulted in the identification of five antimicrobial peptides structurally related to the magainins (magainin-M1 and -M2), xenopsin-precursor fragments (XPF-M1) and caerulein-precursor fragments (CPF-M1 and -M2) previously found in skin secretions of other Xenopus species. A cyclic peptide (WCPPMIPLCSRF.NH2) containing the RFamide motif was also isolated that shows limited structural similarity to the tigerinins, previously identified only in frogs of the Dicroglossidae family. The components identified in skin secretions from X. muelleri from the western range comprised one magainin (magainin-MW1), one XPF peptide (XPF-MW1), two peptides glycine-leucine amide (PGLa-MW1 and -MW2), and three CPF peptides (CPF-MW1, -MW2 and -MW3). Comparison of the primary structures of these peptides suggest that western population of X. muelleri is more closely related to X. borealis than to X. muelleri consistent with its proposed designation as a separate species. The CPF peptides showed potent, broad-spectrum activity against reference strains of bacteria (MIC 3-25 µM), but were hemolytic against human erythrocytes.


Subject(s)
Amphibian Proteins/analysis , Antimicrobial Cationic Peptides/analysis , Bodily Secretions/chemistry , Genetic Speciation , Proteomics/methods , Skin/metabolism , Xenopus/metabolism , Africa, Eastern , Africa, Western , Amino Acid Sequence , Amphibian Proteins/chemistry , Amphibian Proteins/pharmacology , Animals , Antimicrobial Cationic Peptides/chemistry , Antimicrobial Cationic Peptides/pharmacology , Candida albicans/drug effects , Candida albicans/growth & development , Chromatography, High Pressure Liquid , Erythrocytes/cytology , Erythrocytes/metabolism , Escherichia coli/drug effects , Escherichia coli/growth & development , Female , Hemolysis/drug effects , Humans , Male , Microbial Sensitivity Tests , Molecular Sequence Data , Phylogeny , Phylogeography , Skin/chemistry , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Staphylococcus aureus/drug effects , Staphylococcus aureus/growth & development , Xenopus/genetics
18.
Peptides ; 32(2): 203-8, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21087647

ABSTRACT

Using a combination of reversed-phase HPLC and electrospray mass spectrometry, peptidomic analysis of norepinephrine-stimulated skin secretions of the American bullfrog Lithobates catesbeianus Shaw, 1802 led to the identification and characterization of five newly described peptides (ranatuerin-1CBb, ranatuerin-2CBc, and -CBd, palustrin-2CBa, and temporin-CBf) together with seven peptides previously isolated on the basis of their antimicrobial activity (ranatuerin-1CBa, ranatuerin-2CBa, brevinin-1CBa, and -1CBb, temporin-CBa, -CBb, and -CBd). The abilities of the most abundant of the purified peptides to stimulate the release of insulin from the rat BRIN-BD11 clonal ß cell line were evaluated. Ranatuerin-2CBd (GFLDIIKNLGKTFAGHMLDKIRCTIGTCPPSP) was the most potent peptide producing a significant stimulation of insulin release (119% of basal rate, P<0.01) from BRIN-BD11 cells at a concentration of 30nM, with a maximum response (236% of basal rate, P<0.001) at a concentration of 3µM. Ranatuerin-2CBd did not stimulate release of the cytosolic enzyme, lactate dehydrogenase at concentrations up to 3µM, indicating that the integrity of the plasma membrane had been preserved. Brevinin-1CBb (FLPFIARLAAKVFPSIICSVTKKC) produced the maximum stimulation of insulin release (285% of basal rate, P<0.001 at 3µM) but the peptide was cytotoxic at this concentration.


Subject(s)
Bodily Secretions/chemistry , Insulin-Secreting Cells/drug effects , Insulin/metabolism , Peptides/analysis , Peptides/pharmacology , Rana catesbeiana/metabolism , Skin/metabolism , Amino Acid Sequence , Amphibian Proteins/analysis , Amphibian Proteins/chemistry , Amphibian Proteins/isolation & purification , Amphibian Proteins/pharmacology , Animals , Antimicrobial Cationic Peptides/analysis , Antimicrobial Cationic Peptides/chemistry , Antimicrobial Cationic Peptides/isolation & purification , Antimicrobial Cationic Peptides/pharmacology , Cell Line , Cell Survival/drug effects , Chromatography, High Pressure Liquid , Insulin Secretion , Insulin-Secreting Cells/metabolism , Molecular Sequence Data , Molecular Weight , Peptides/chemistry , Peptides/isolation & purification , Protein Isoforms/analysis , Protein Isoforms/chemistry , Protein Isoforms/isolation & purification , Protein Isoforms/pharmacology , Proteins/analysis , Proteins/chemistry , Proteins/isolation & purification , Proteins/pharmacology , Rats , Spectrometry, Mass, Electrospray Ionization
19.
Zygote ; 17(4): 329-40, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19500442

ABSTRACT

SummaryBufo arenarum oocytes are oviposited surrounded by jelly coats, one component of the extracellular matrix required for fertilization. The secretion, released to the oviductal lumen, was analysed by SDS-PAGE. The coomassie blue staining evidenced an electrophoretic pattern with molecules ranging between 300 and 19 kDa that showed variations in their secretion profiles during the sexual cycle. In the preovulatory period the densitometric analysis showed the presence of nine peaks with marked predominance of the 74 kDa molecule. Once ovulation has occurred, the jelly coats become arranged around the oocytes during their transit throughout the oviductal pars convoluta (PC), revealing the addition of three proteins only observed during this period, which suggests a differential secretion. Some of these proteins could not diffuse under any extraction treatment, indicating for them a structural or in situ function. Proteins of low molecular mass diffused totally while others showed a partial diffusing capacity. After ovulation a marked decrease in the relative amount of all the proteins released to the lumen, especially the 74 kDa protein, could be detected. During this period, unlike the other stages of the sexual cycle, a differential secretion pattern was observed along the PC. The histochemical analysis performed during the ovulatory period showed the presence of glycoconjugates including both acidic and neutral groups. The present results are in agreement with previous ultrastructural and histochemical studies that describe the role of Bufo arenarum jelly coats in fertilization.


Subject(s)
Amphibian Proteins/analysis , Bufo arenarum/metabolism , Extracellular Matrix/chemistry , Oocytes/chemistry , Oviducts/metabolism , Animals , Electrophoresis, Polyacrylamide Gel , Female
20.
Rapid Commun Mass Spectrom ; 23(9): 1241-8, 2009 May.
Article in English | MEDLINE | ID: mdl-19308951

ABSTRACT

A high-performance liquid chromatography nano-electrospray ionization Fourier transform mass spectrometry (HPLC/nanoESI-FTMS) approach involving recording of collision-activated dissociation (CAD) and electron-capture dissociation (ECD) spectra of an intact sample and two its modifications after performic oxidation and reduction followed by carboxamidomethylation helps to establish peptide profiles in the crude secretion of frog species at mid-throughput level, including de novo sequencing. The proposed derivatization procedures allow increasing of the general sequence coverage in the backbone, providing complementary information and, what is more important, reveal the amino acid sequence in the cystine ring ('rana box'). Thus purely mass spectrometric efficient sequencing becomes possible for longer than usual proteolytic peptides. Seventeen peptides belonging to four known families were identified in the secretion of the European brown frog Rana arvalis inhabiting the Moscow region in Russia. Ranatuerins, considered previously a unique feature of the North American species, as well as a new melittin-related peptide, are worth special mention. The developed approach was previously successfully used for the identification of peptides in the skin secretion of the Caucasian green frog Rana ridibunda.


Subject(s)
Amphibian Proteins/analysis , Chromatography, High Pressure Liquid/methods , Peptides/analysis , Ranidae/physiology , Skin/metabolism , Spectrometry, Mass, Electrospray Ionization/methods , Amino Acid Sequence , Amphibian Proteins/metabolism , Animals , Anti-Infective Agents/analysis , Anti-Infective Agents/metabolism , Female , Male , Molecular Sequence Data , Oxidation-Reduction , Peptides/metabolism , Russia
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