Integrated Methods in Protein Biochemistry: Part B | Buch | 978-0-323-99264-0 | sack.de

Buch, Englisch, 412 Seiten, Format (B × H): 152 mm x 229 mm, Gewicht: 790 g

Integrated Methods in Protein Biochemistry: Part B

Buch, Englisch, 412 Seiten, Format (B × H): 152 mm x 229 mm, Gewicht: 790 g

ISBN: 978-0-323-99264-0
Verlag: William Andrew Publishing


Integrated Methods in Protein Biochemistry: Part B, Volume 678 in the Methods in Enzymology series, highlights new advances in the field, with this new volume presenting interesting chapters on a variety of topics, including Precise modification of native proteins, purification, and analysis of bioconjugates, NanoBiT-based methods to monitor the activation and modulation of RTKs, The interplay of G-protein ß? subunit and PLC-ß enzyme in PIP2 hydrolysis and downstream signaling, Structure and function of bacterial secretion system, Tools and protocols for probing protein sumoylation, Spectroscopic analysis of cysteine dioxygenase: a mammalian thiol-dioxygenase, DeGlyPHER: MS-based analysis of viral spike N-glycoforms, and more.

Additional sections cover Covalent protein painting: MS-based protein footprinting, Characterization of GPCR signaling complexes using negative-staining electron microscopy, Probing protein misfolding and dissociation with free electron laser, Optimized protocol for the characterization of Cas12a activities, Proximity proteomics for the identification and characterization of extracellular vesicles, Structural and Functional characterization of lytic polysaccharide monooxygenases, and much more.
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Zielgruppe


<p>Biochemists, biophysicists, molecular biologists, analytical chemists, and physiologists</p>

Weitere Infos & Material


1. Precise modification of native proteins, purification, and analysis of bioconjugates
2. NanoBiT-based methods to monitor the activation and modulation of RTKs
3. The interplay of G-protein ß? subunit and PLC-ß enzyme in PIP2 hydrolysis and downstream signaling
4. Structure and function of bacterial secretion system
5. Probing the structure and function of N-acetylmannosamine-6-phosphate 2-epimerase
6. Tools and protocols for probing protein sumoylation
7. Spectroscopic analysis of cysteine dioxygenase: a mammalian thiol-dioxygenase
8. DeGlyPHER: MS-based analysis of viral spike N-glycoforms
9. Covalent protein painting: MS-based protein footprinting
10. Characterization of GPCR signaling complexes using negative-staining electron microscopy
11. Probing protein misfolding and dissociation with free electron laser
12. Optimized protocol for the characterization of Cas12a activities
13. Proximity proteomics for the identification and characterization of extracellular vesicles
14. Structural and Functional characterization of lytic polysaccharide monooxygenases
15. Characterization of RRE domain in RiPP biosynthesis
16. Structural and mechanistic insights into ferrous iron import and export systems
17. Testing anti-cancer drugs with holographic Incoherent light source quantitative phase imaging
18. Gel-based sample preparation methods for top-down native/cross-linking mass spectrometry
19. Identification and characterization of natural products and their interacts with anti-mycobacterial drug target proteins
20. Integrated studies on ageing-related proteins extending life span in yeast
21. An optimized pipeline for global selenoproteome analysis
22. High-throughput screening and evolution of carbohydrate-active enzymes
23. Regulation of enzymes with light using unnatural amino acids
24. An optimized protocol for modular cloning to rapidly assemble expression vectors for MS-based orthogonal interactomics studies
25. Nucleotide-linked resins to identify new nucleotide-binding proteins using proteomics
26. Phospho-proteomic analysis of immune cells expressing chimeric antigen receptors
27. Novel strategies for targeting ubiquitin conjugation machinery using synthetic molecules
28. Reconstitution of the MLL1 complex and probing methyltransferase activity
29. Probing cellular aspects of endocytosis and phagocytosis with super-resolution microscopy
30. Structural and functional analysis of mono-copper enzymes from fungal species


Shukla, Arun K.
Dr. Arun K. Shukla is a world leader in the field of GPCR biology and he is currently a Professor in the Department of Biological Sciences and Bioengineering at the Institute of Technology, Kanpur in India. Dr. Shukla's research program is focused on understanding the structure, function and regulation of G protein-coupled receptors with a long-term of designing novel therapeutics with minimized side-effects.


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