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| 001 | 235123 | ||
| 003 | ES-VaUE | ||
| 005 | 20221220020645.0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 100301s2008 xxu| s |||| 0|eng d | ||
| 020 | _a9781597454193 | ||
| 024 | 7 |
_a10.1007/978-1-59745-419-3 _2doi |
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| 040 |
_aES-MaUEC _bspa _cES-MaUEC |
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| 245 | 1 | 0 |
_aPeptide-Based Drug Design _cedited by Laszlo Otvos. |
| 250 | _a1st edition 2008 | ||
| 264 | 1 |
_aTotowa, NJ _bHumana Press _c2008 |
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| 300 |
_a1 recurso en línea (XI, 303 páginas) _b |
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| 336 |
_atexto _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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| 338 |
_arecurso electrónico _bcr _2rdacarrier |
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| 347 |
_aarchivo de texto _bPDF |
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| 490 | 0 |
_aMethods in Molecular Biology _x1940-6029 _v494 |
|
| 505 | 0 | _aPeptide-Based Drug Design: Here and Now -- Strategies for the Discovery, Isolation, and Characterization of Natural Bioactive Peptides from the Immune System of Invertebrates -- Sequence Analysis of Antimicrobial Peptides by Tandem Mass Spectrometry -- The Spot Technique: Synthesis and Screening of Peptide Macroarrays on Cellulose Membranes -- Analysis of A? Interactions Using ProteinChip Technology -- NMR in Peptide Drug Development -- Molecular Dynamics Simulations of Peptides -- Short Linear Cationic Antimicrobial Peptides: Screening, Optimizing, and Prediction -- Investigating the Mode of Action of Proline-Rich Antimicrobial Peptides Using a Genetic Approach: A Tool to Identify New Bacterial Targets Amenable to the Design of Novel Antibiotics -- Serum Stability of Peptides -- Preparation of Glycosylated Amino Acids Suitable for Fmoc Solid-Phase Assembly -- Synthesis of O-Phosphopeptides on Solid Phase -- Peptidomimetics: Fmoc Solid-Phase Pseudopeptide Synthesis -- Synthesis of Toll-Like Receptor-2 Targeting Lipopeptides as Self-Adjuvanting Vaccines -- Synthesis of a Multivalent, Multiepitope Vaccine Construct -- Cysteine-Containing Fusion Tag for Site-Specific Conjugation of Therapeutic and Imaging Agents to Targeting Proteins. | |
| 520 | _aDue to their high specificity and low toxicity profile, peptides have once again become central to the development of new drugs. In Peptide-Based Drug Design: Methods and Protocols, expert researchers provide a handbook which offers a selection of research and production tools suitable for transforming a promising protein fragment or stand-alone native peptide into a pharmaceutically acceptable composition. The volume delves into contemporary, cutting-edge subjects such as hit isolation and target validation, computer-aided design, sequence modifications to satisfy pharmacologists, in vivo stability and imaging, and the actual production of difficult sequences. Written in the highly successful Methods in Molecular Biology™ series format, chapters include readily reproducible, step-by-step laboratory protocols, lists of materials, and the Notes section, which highlights tips on troubleshooting and avoiding known pitfalls. Comprehensive and up-to-date, Peptide-Based Drug Design: Methods and Protocols shows its subject to be an independent science on the rise, and provides scientists with a clear, concise guide for continuing this vital research. | ||
| 700 | 1 |
_aOtvos, Laszlo _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt |
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| 776 | 0 | 8 |
_iPrinted edition: _z9781603278720 |
| 776 | 0 | 8 |
_iPrinted edition: _z9781617378690 |
| 776 | 0 | 8 |
_iPrinted edition: _z9781588299901 |
| 856 | 4 | 0 |
_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-1-59745-419-3 _z(usuarios Universidad Europea de Valencia) |
| 942 |
_2lcc _cLE |
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| 988 | _aSpringer_Protocols_2008 | ||
| 999 |
_c235123 _d235123 |
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