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Relevant bibliographies by topics / Peptides with enantiomeric sequence

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Academic literature on the topic 'Peptides with enantiomeric sequence'

Author: Grafiati

Published: 22 February 2023

Last updated: 31 July 2025

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Journal articles on the topic "Peptides with enantiomeric sequence"

1

Urban, Jennifer M., Janson Ho, Gavin Piester, Riqiang Fu та Bradley L. Nilsson. "Rippled β-Sheet Formation by an Amyloid-β Fragment Indicates Expanded Scope of Sequence Space for Enantiomeric β-Sheet Peptide Coassembly". Molecules 24, № 10 (2019): 1983. http://dx.doi.org/10.3390/molecules24101983.

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In 1953, Pauling and Corey predicted that enantiomeric β-sheet peptides would coassemble into so-called “rippled” β-sheets, in which the β-sheets would consist of alternating l- and d-peptides. To date, this phenomenon has been investigated primarily with amphipathic peptide sequences composed of alternating hydrophilic and hydrophobic amino acid residues. Here, we show that enantiomers of a fragment of the amyloid-β (Aβ) peptide that does not follow this sequence pattern, amyloid-β (16–22), readily coassembles into rippled β-sheets. Equimolar mixtures of enantiomeric amyloid-β (16–22) peptide

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Santamaría, Carlos, Silda Larios, Steve Quirós, et al. "Bactericidal and Antiendotoxic Properties of Short Cationic Peptides Derived from a Snake Venom Lys49 Phospholipase A2." Antimicrobial Agents and Chemotherapy 49, no. 4 (2005): 1340–45. http://dx.doi.org/10.1128/aac.49.4.1340-1345.2005.

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ABSTRACT The activities of short synthetic, nonhemolytic peptides derived from the C-terminal region of myotoxin II, a catalytically inactive phospholipase A2 homologue present in the venom of the snake Bothrops asper, have been shown to reproduce the bactericidal activity of the parent protein. They combine cationic and hydrophobic-aromatic amino acids, thus functionally resembling the antimicrobial peptides of innate defenses. This study evaluated the antimicrobial and antiendotoxic properties of a 13-mer derivative peptide of the C-terminal sequence from positions 115 to 129 of myotoxin II,

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Novelli, Federica, Serena De Santis, Stefano Morosetti, Mattia Titubante, Giancarlo Masci, and Anita Scipioni. "Peptides with regularly alternating enantiomeric sequence: From ion channel models to bioinspired nanotechnological applications." Peptide Science 110, no. 5 (2018): e24043. http://dx.doi.org/10.1002/pep2.24043.

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Strömstedt, Adam A., Mukesh Pasupuleti, Artur Schmidtchen, and Martin Malmsten. "Evaluation of Strategies for Improving Proteolytic Resistance of Antimicrobial Peptides by Using Variants of EFK17, an Internal Segment of LL-37." Antimicrobial Agents and Chemotherapy 53, no. 2 (2008): 593–602. http://dx.doi.org/10.1128/aac.00477-08.

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ABSTRACT Methods for increasing the proteolytic stability of EFK17 (EFKRIVQRIKDFLRNLV), a new peptide sequence with antimicrobial properties derived from LL-37, were evaluated. EFK17 was modified by four d-enantiomer or tryptophan (W) substitutions at known protease cleavage sites as well as by terminal amidation and acetylation. The peptide variants were studied in terms of proteolytic resistance, antibacterial potency, and cytotoxicity but also in terms their adsorption at model lipid membranes, liposomal leakage generation, and secondary-structure behavior. The W substitutions resulted in a

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Agostini, Luigi, and Stefano Morosetti. "In silico Design of Glyco-D,L-Peptide Antiviral Molecules." Journal of Computational Biophysics and Chemistry 21, no. 03 (2022): 349–60. http://dx.doi.org/10.1142/s2737416522500132.

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Background: Most licensed antiviral drugs are nucleoside analogs. A recent research focuses on blocking a virus from entering the cells in the viral cell adsorption/entry stage. In this entry mechanism, the glycans present on the viral surface play a fundamental role. Homochiral L-peptides acting this fusion mechanism have shown some inhibition of viral infection. Peptides with regularly alternating enantiomeric sequence (L,D-peptides) can assume structures that are not accessible to the corresponding homochiral molecules. Furthermore, L,D-peptides are less sensitive to enzymatic digestion. Ai

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De Santis, Pasquale, Stefano Morosetti, and Anita Scipioni. "Peptides with Regular Enantiomeric Sequences: A Wide Class of Modular Self-Assembling Architectures." Journal of Nanoscience and Nanotechnology 7, no. 7 (2007): 2230–38. http://dx.doi.org/10.1166/jnn.2007.644.

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Cavaco, Marco, Javier Valle, Ruben da Silva, et al. "DPepH3, an Improved Peptide Shuttle for Receptor-independent Transport Across the Blood-Brain Barrier." Current Pharmaceutical Design 26, no. 13 (2020): 1495–506. http://dx.doi.org/10.2174/1381612826666200213094556.

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Background: The use of peptides as drug carriers across the blood-brain barrier (BBB) has increased significantly during the last decades. PepH3, a seven residue sequence (AGILKRW) derived from the α-helical domain of the dengue virus type-2 capsid protein, translocates across the BBB with very low toxicity. Somehow predictably from its size and sequence, PepH3 is degraded in serum relatively fast. Among strategies to increase peptide half-life (t1/2), the use of the enantiomer (wholly made of D-amino acid residues) can be quite successful if the peptide interacts with a target in non-stereosp

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Matsuo, Naoki, Natsuko Goda, Takeshi Tenno, and Hidekazu Hiroaki. "Cryoprotective activities of FK20, a human genome-derived intrinsically disordered peptide against cryosensitive enzymes without a stereospecific molecular interaction." PeerJ Physical Chemistry 3 (December 14, 2021): e20. http://dx.doi.org/10.7717/peerj-pchem.20.

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Background Intrinsically disordered proteins (IDPs) have been shown to exhibit cryoprotective activity toward other cellular enzymes without any obvious conserved sequence motifs. This study investigated relationships between the physical properties of several human genome-derived IDPs and their cryoprotective activities. Methods Cryoprotective activity of three human-genome derived IDPs and their truncated peptides toward lactate dehydrogenase (LDH) and glutathione S-transferase (GST) was examined. After the shortest cryoprotective peptide was defined (named FK20), cryoprotective activity of

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DÍAZ-ACHIRICA, Pilar, Josep UBACH, Almudena GUINEA, David ANDREU, and Luis RIVAS. "The plasma membrane of Leishmania donovani promastigotes is the main target for CA(1–8)M(1–18), a synthetic cecropin A–melittin hybrid peptide." Biochemical Journal 330, no. 1 (1998): 453–60. http://dx.doi.org/10.1042/bj3300453.

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Reports on the lethal activity of animal antibiotic peptides have largely focused on bacterial rather than eukaryotic targets. In these, involvement of internal organelles as well as mechanisms different from those of prokaryotic cells have been described. CA(1-8)M(1-18) is a synthetic cecropin A-melittin hybrid peptide with leishmanicidal activity. Using Leishmania donovani promastigotes as a model system we have studied the mechanism of action of CA(1-8)M(1-18), its two parental peptides and two analogues. At micromolar concentration CA(1-8)M(1-18) induces a fast permeability to H+/OH-, coll

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Czerwenka, Christoph, and Wolfgang Lindner. "Enantiomer discrimination of peptides by tandem mass spectrometry: influence of the peptide sequence on chiral recognition." Rapid Communications in Mass Spectrometry 18, no. 22 (2004): 2713–18. http://dx.doi.org/10.1002/rcm.1671.

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Dissertations / Theses on the topic "Peptides with enantiomeric sequence"

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Wong, Kim Kai Wai. "Synthesis of silicon functionalised cyclic peptides for enantiomeric separations." Thesis, University of Bath, 1990. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278284.

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Kwok, Hoi-shan, and 郭凱珊. "The comparison of biological properties of L- and D-enantiomeric antimicrobial peptides." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/206507.

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Antibiotics have been used widely for the treatment of bacterial infections for over half a century. However, the emergence of resistance to antibiotics has aroused public health concern, leading to the development of antimicrobial peptides (AMPs) as potential alternative therapeutic agents against bacterial infections. AMPs are naturally found in many species and have important roles in our innate immune defense systems. AMPs are usually cationic amphipathic peptides with membrane destabilizing property. They have a relatively broad spectrum of antimicrobial activity and pathogens are less li

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Cherry, Melissa A. "Sequence dependence of the activity of amphipathic peptides." View electronic thesis, 2008. http://dl.uncw.edu/etd/2008-2/rp/cherrym/melissacherry.pdf.

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Wang, Yuqin. "Protein and lipid interactions of mammalian antibacterial peptides /." Stockholm, 2001. http://diss.kib.ki.se/2001/91-628-4698-1/.

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Zhang, Mingzhen. "Multiscale Molecular Simulations of Cross-sequence Interactions between Amyloid Peptides." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1490711960550386.

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Yan, Fu. "Detailed analysis of sequence requirements within 2A translational recoding peptides." Thesis, University of Newcastle upon Tyne, 2014. http://hdl.handle.net/10443/2654.

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2A sequences are short 20 ~30 amino acid peptides initially characterised from foot and mouth disease virus (FMDV), but also encoded in a range of Picornaviruses and other viruses as well as non-LTR retrotransposons in a broad range of organisms. They direct a translational recoding event in which ribosomes that have reached the final codon of the 2A sequence pause and terminate translation in the absence of a stop codon and then restart translation. The effect is to separate a single ORF into 2 polypeptides, between the final 2 amino acids (glycine and proline) of 2A, ‘skipping’ a peptide bon

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Quan, Cynthia S. "Cytotoxic activity of designed peptides based on the human erythropoietin sequence." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0021/MQ54097.pdf.

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Hicks, Matthew Raymond. "Coiled-coil assembly by proteins and peptides with unusual sequence motifs." Thesis, University of Sussex, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311349.

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Jiang, Nan Verfasser], and Dieter [Akademischer Betreuer] [Willbold. "Preclinical pharmacokinetics and cerebral distribution of D-enantiomeric peptides for the treatment of Alzheimer’s disease / Nan Jiang ; Betreuer: Dieter Willbold." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2018. http://d-nb.info/1150918845/34.

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Jiang, Nan [Verfasser], and Dieter [Akademischer Betreuer] Willbold. "Preclinical pharmacokinetics and cerebral distribution of D-enantiomeric peptides for the treatment of Alzheimer’s disease / Nan Jiang ; Betreuer: Dieter Willbold." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2018. http://d-nb.info/1150918845/34.

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Books on the topic "Peptides with enantiomeric sequence"

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1927-, Jollès Pierre, ed. D-amino acids in sequences of secreted peptides of multicellular organisms. Birkhäuser Verlag, 1998.

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2

G, Allen. Sequencing of proteins and peptides. Elsevier/North-Holland, 1989.

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1934-, Bhown Ajit S., ed. Protein/peptide sequence analysis: Current methodologies. CRC Press, 1988.

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Quan, Cynthia S. Cytotoxic activity of designed peptides based on the human erythropoietin sequence. National Library of Canada, 2000.

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5

T, Matsudaira Paul, ed. A Practical guide to protein and peptide purification for microsequencing. Academic Press, 1989.

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6

Bodanszky, Miklos. Peptide chemistry: A practical textbook. Springer-Verlag, 1988.

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R, Marshak Daniel, and Protein Society, eds. Techniques in protein chemistry VII. Academic Press, 1996.

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Bodanszky, Miklos. Peptide chemistry: A practical textbook. 2nd ed. Springer-Verlag, 1993.

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9

Victor, Brantl, Teschemacher Hansjörg, and International Symposium on [Beta]-Casomorphins and Related Peptides (2nd : 1991 : Titisee, Germany), eds. [Beta]-casomorphins and related peptides: Recent developments. VCH, 1994.

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10

S, Lipton Mary, and Paša-Tolić Ljiljana, eds. Mass spectrometry of proteins and peptides: Methods and protocols. 2nd ed. Humana, 2009.

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Book chapters on the topic "Peptides with enantiomeric sequence"

1

Brückner, Hans, Ingrid Bosch, Sibylle Kühne, and Sibylle Zivny. "Analysis and enantiomeric resolution of α-alkyl-α-amino acids." In Peptides. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-010-9595-2_56.

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Tjoeng, F. Siong, Kam F. Fok, Mark E. Zupec, et al. "Peptide mimetics of the RGD sequence." In Peptides. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_302.

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Gierasch, Lila M., Martha S. Briggs, and C. James McKnight. "Role of the signal sequence in protein secretion." In Peptides. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-010-9595-2_94.

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Chandrasekar, Ramamurthy, and Michael H. Klapper. "Synthesis of peptides containing a diethylglycine repeat sequence." In Peptides. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_97.

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Valerio, R. M., A. M. Bray, H. M. Geysen, and N. J. Maeji. "“Difficult” sequence prediction: a requirement for multiple peptide synthesis?" In Peptides. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_345.

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Graddis, Tom, and Irwin Chaiken. "Designing homodimers and heterodimers with sequence simplified leucine zipper models." In Peptides. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_132.

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Chen, Zheng-ying, Xue-jun Fan, Xiao-jie Dong, and Xian-kai Ma. "Exploratory studies on sequence-dependence in solid phase peptide synthesis." In Peptides. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-010-9066-7_91.

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Arar, K., M. Monsigny, and R. Mayer. "Synthesis of peptide-oligonucleotide hybrids containing a kdel signal sequence." In Peptides. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_58.

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Chaiken, Irwin, Shoji Ando, Giorgio Fassina, and Yechiel Shai. "Sequence simplification and randomization and the design of peptide recognition surfaces." In Peptides. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-010-9595-2_107.

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Rötzschke, Olaf, Kirsten Falk, Hansjörg Schild, et al. "Sequence motifs of peptides eluted from MHC molecules are allele specific." In Peptides. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_336.

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Conference papers on the topic "Peptides with enantiomeric sequence"

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Nilsson, Bradley L., Danielle M. Raymond та Jade J. Welch. "Rippled β-Sheet Fibrils from Coassembled Enantiomeric Amphipathic Peptides as Potential Microbicide Biomaterials". У The 24th American Peptide Symposium. Prompt Scientific Publishing, 2015. http://dx.doi.org/10.17952/24aps.2015.033.

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Yu, Jen-Chieh, Kuan Ni, and Ching-Tai Chen. "Sequence-based Prediction of Antimicrobial Peptides with CatBoost Classifier." In 2022 IEEE 22nd International Conference on Bioinformatics and Bioengineering (BIBE). IEEE, 2022. http://dx.doi.org/10.1109/bibe55377.2022.00053.

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Wennemers, Helma, Matteo Conza, and Matthias Nold. "Sequence-selective Binding of Small Peptides by Two-armed Receptors." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01904.

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Roque-Borda, Cesar, Fernando Pavan, Anna Toledo Borgues, Janaína Texeira Costa de Pontes, Eduardo Vicente, and Saulo Santesso Garrido. "B1CTcu5 analogs as promising antimicrobial peptides, replacing the sequence cysteine." In 7th International Electronic Conference on Medicinal Chemistry. MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11576.

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Unksov, Ivan N., Lena K. Müller, Hanna Zdhannova, et al. "Metal complexes of ATCUN-like peptides for sequence-specific DNA cleavage." In 37th European Peptide Symposium. The European Peptide Society, 2024. http://dx.doi.org/10.17952/37eps.2024.p1064.

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Li, Bowen, Hen Chen, and Bifang He. "CD47BPFormer: A Sequence-Based Predictor Based on Transformer to Identify CD47 Binding Peptides." In 2023 6th International Conference on Information Communication and Signal Processing (ICICSP). IEEE, 2023. http://dx.doi.org/10.1109/icicsp59554.2023.10390848.

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Abioye, Raliat, Caleb Acquah, Chibuike Udenigwe, Nico Huttmann, and Pei Chun Queenie Hsu. "Self-assembly and hydrogelation properties of egg white-derived peptides." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/jzku2300.

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Functional foods are gaining traction as a source of peptides possessing hydrogelation properties. Analysis of peptides (n=429) in egg white protein hydrolysates resulted in the identification of six peptides: IFYCPIAIM, NIFYCPIAIM, VLVNAIVFKGL, YCPIAIMSA, MMYQIGLF, and VYSFSLASRL as prominent self-assembly candidates based on prediction of their aggregation-prone segments. The objective of this study was to characterize the hydrogel formed via self-assembly of the peptides. Of the six peptides studied, NIFYCPIAIM and MMYQIGLF showed promising self-assembly and hydrogelation properties. Thiofl

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Fresslnaud, E., J. E. Sadler, J. P. Girma, H. R. Baumgartner, and D. Meyer. "SYNTHETIC RGD-CONTAINING PEPTIDES OF VON WILLEBRAND FACTOR INHIBIT PLATELET ADHESION TO COLLAGEN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643591.

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The Arg-Gly-Asp (RGD) sequence is common to fibrinogen (Fg), fibronectin (Fn) and von Willebrand Factor (vWF). RGD-containing peptides compete for binding of these adhesive proteins to platelet membrane GPIIb/IIIa and inhibit thrombin-induced platelet aggregation as does an unrelated dodecapeptide from the γ Fg COOH terminus (γFg 400-411). We compared in flowing blood the effect of γ Fg 400-411 and of 3 synthetic peptides derived from the sequence of human vWF upon platelet adhesion to collagen. The 3 vWF peptides (13 or 18 aminoacids) contained an RGD sequence in the NH2 (peptide 03), central

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Veltri, Daniel, Uday Kamath, and Amarda Shehu. "A novel method to improve recognition of antimicrobial peptides through distal sequence-based features." In 2014 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2014. http://dx.doi.org/10.1109/bibm.2014.6999187.

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Yamamoto, K., H. Kawasaki, K. Suzuki, K. Tanoue, G. Kosaki, and H. Yamazaki. "AMINO ACID SEQUENCE OF THE THROMBIN-BINDING SITE ON PLATELET GLYCOPROTEIN Ib." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642924.

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Amino acid sequence of the thrombin-binding site on platelet glycoprotein (GP) Ib was determined and the effects of the synthesized analogous peptides on thrombin-induced aggregation were studied. Crude platelet membrane fraction solubilized with 5mM dithiothreitol and 0.2% Tween 20 was applied to a WGA-Sepharose. The bound fractions were eluted with 0.3M N-actylglucosamine, then applied to a TM60 ( a monoclonal antibody against GP Ib)-Affi-gel column. Only one GP was bound to the column and was eluted with 50mM glycine-HCl, pH3.0, containing 0.2% Tween 20. SDS-PAGE showed a single band of 130

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Reports on the topic "Peptides with enantiomeric sequence"

1

Storrs, R. W. Structural studies of polypeptides: Mechanism of immunoglobin catalysis and helix propagation in hybrid sequence, disulfide containing peptides. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6707762.

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Storrs, Richard Wood. Structural studies of polypeptides: Mechanism of immunoglobin catalysis and helix propagation in hybrid sequence, disulfide containing peptides. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10131755.

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Rafaeli, Ada, Russell Jurenka, and Daniel Segal. Isolation, Purification and Sequence Determination of Pheromonotropic-Receptors. United States Department of Agriculture, 2003. http://dx.doi.org/10.32747/2003.7695850.bard.

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Moths constitute a major group of pest insects in agriculture. Pheromone blends are utilised by a variety of moth species to attract conspecific mates, which is under circadian control by the neurohormone, PBAN (pheromone-biosynthesis-activating neuropeptide). Our working hypothesis was that, since the emission of sex-pheromone is necessary to attract a mate, then failure to produce and emit pheromone is a potential strategy for manipulating adult moth behavior. The project aimed at identifying, characterising and determining the sequence of specific receptors responsible for the interaction w

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Barefoot, Susan F., Bonita A. Glatz, Nathan Gollop, and Thomas A. Hughes. Bacteriocin Markers for Propionibacteria Gene Transfer Systems. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7573993.bard.

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The antibotulinal baceriocins, propionicin PLG-1 and jenseniin G., were the first to be identified, purified and characterized for the dairy propionibaceria and are produced by Propionibacterium thoenii P127 and P. thoenii/jensenii P126, respectively. Objectives of this project were to (a) produce polyclonal antibodies for detection, comparison and monitoring of propionicin PLG-1; (b) identify, clone and characterize the propionicin PLG-1 (plg-1) and jenseniin G (jnG) genes; and (3) develop gene transfer systems for dairy propionibacteria using them as models. Polyclonal antibodies for detecti

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Mevarech, Moshe, Jeremy Bruenn, and Yigal Koltin. Virus Encoded Toxin of the Corn Smut Ustilago Maydis - Isolation of Receptors and Mapping Functional Domains. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7613022.bard.

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Ustilago maydis is a fungal pathogen of maize. Some strains of U. maydis encode secreted polypeptide toxins capable of killing other susceptible strains of U. maydis. Resistance to the toxins is conferred by recessive nuclear genes. The toxins are encoded by genomic segments of resident double-strande RNA viruses. The best characterized toxin, KP6, is composed of two polypeptides, a and b, which are not covalently linked. It is encoded by P6M2 dsRNA, which has been cloned, sequenced and expressed in a variety of systems. In this study we have shown that the toxin acts on the membranes of sensi

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Rafaeli, Ada, Russell Jurenka, and Chris Sander. Molecular characterisation of PBAN-receptors: a basis for the development and screening of antagonists against Pheromone biosynthesis in moth pest species. United States Department of Agriculture, 2008. http://dx.doi.org/10.32747/2008.7695862.bard.

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The original objectives of the approved proposal included: (a) The determination of species- and tissue-specificity of the PBAN-R; (b) the elucidation of the role of juvenile hormone in gene regulation of the PBAN-R; (c) the identificationof the ligand binding domains in the PBAN-R and (d) the development of efficient screening assays in order to screen potential antagonists that will block the PBAN-R. Background to the topic: Moths constitute one of the major groups of pest insects in agriculture and their reproductive behavior is dependent on chemical communication. Sex-pheromone blends are

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Rafaeli, Ada, and Russell Jurenka. Molecular Characterization of PBAN G-protein Coupled Receptors in Moth Pest Species: Design of Antagonists. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7593390.bard.

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The proposed research was directed at determining the activation/binding domains and gene regulation of the PBAN-R’s thereby providing information for the design and screening of potential PBAN-R-blockers and to indicate possible ways of preventing the process from proceeding to its completion. Our specific aims included: (1) The identification of the PBAN-R binding domain by a combination of: (a) in silico modeling studies for identifying specific amino-acid side chains that are likely to be involved in binding PBAN with the receptor and; (b) bioassays to verify the modeling studies using mut

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