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020 _a9780750330398
_qebook
020 _a9780750330381
_qmobi
020 _z9780750330374
_qprint
020 _z9780750330404
_qmyPrint
024 7 _a10.1088/978-0-7503-3039-8
_2doi
035 _a(CaBNVSL)thg00082502
035 _a(OCoLC)1259501142
040 _aCaBNVSL
_beng
_erda
_cCaBNVSL
_dCaBNVSL
050 4 _aQP801.P64
_bS567 2021eb
072 7 _aPHVN
_2bicssc
072 7 _aSCI009000
_2bisacsh
082 0 4 _a574.19/283
_223
245 0 0 _aSingle-particle cryo-EM of biological macromolecules /
_cedited by Robert M. Glaeser, Eva Nogales, Wah Chiu.
264 1 _aBristol [England] (Temple Circus, Temple Way, Bristol BS1 6HG, UK) :
_bIOP Publishing,
_c[2021]
300 _a1 online resource (various pagings) :
_billustrations (some color).
336 _atext
_2rdacontent
337 _aelectronic
_2isbdmedia
338 _aonline resource
_2rdacarrier
490 1 _a[IOP release $release]
490 1 _aBiophysical Society-IOP series
490 1 _aIOP ebooks. [2021 collection]
500 _a"Version: 20210205"--Title page verso.
504 _aIncludes bibliographical references.
505 0 _a1. Introduction and overview -- 1.1. Visualizing biological molecules to understand life's principles -- 1.2. Recovery of 3D structures from images of weak-phase objects
505 8 _a2. Sample preparation -- 2.1. Overview -- 2.2. Initial screening of samples in negative stain -- 2.3. Standard method of making grids for cryo-EM -- 2.4. Requirement to make very thin specimens for cryo-EM -- 2.5. Current strategies for optimizing preparation of cryo-grids
505 8 _a3. Data collection -- 3.1. Overview -- 3.2. Radiation damage in cryo-EM -- 3.3. Low-dose protocols for recording images -- 3.4. Practical considerations : defocus, stigmation, coma-free illumination, and phase plates -- 3.5. Practical considerations : movie-mode data acquisition
505 8 _a4. Data processing -- 4.1. Overview -- 4.2. Automated extraction of particles -- 4.3. CTF estimation and image correction (restoration) -- 4.4. Merging data from structurally homogeneous subsets -- 4.5. 3D classification of structurally heterogeneous particles -- 4.6. Preferred orientation : how to recognize and deal with adverse effects -- 4.7. B factors and map sharpening -- 4.8. Optical aberrations and Ewald sphere curvature
505 8 _a5. Map validation -- 5.1. Overview -- 5.2. Measures of resolution : FSC and local resolution -- 5.3. Recognizing the effect of bias and over-fitting -- 5.4. Estimates of alignment accuracy -- 5.5. Discussion
505 8 _a6. Model building and validation -- 6.1. Overview -- 6.2. Using known components or homologs : model building -- 6.3. Building atomistic models in cryo-EM density maps -- 6.4. Quality evaluation of cryo-EM map-derived models -- 6.5. How algorithms from crystallography are helping electron cryo-microscopy -- 6.6. Archiving structures and data.
520 3 _aThis edited book is written for students, postdocs and established investigators who want to enter the field of single-particle cryo-EM. This is a recently developed method to determine high-resolution structures of biological macromolecules. A major strength is the fact that cryo-EM does not require prior crystallization of protein complexes. It is especially well suited for larger complexes and molecular machines. This book provides a comprehensive, accessible and authoritative introduction to the field. It covers all necessary background, ranging from the underlying concepts to practical aspects such as specimen preparation, data collection, data analysis, and the final validation of results.
521 _aBeginning scientists in academia, pharma, and biotech.
530 _aAlso available in print.
538 _aMode of access: World Wide Web.
538 _aSystem requirements: Adobe Acrobat Reader, EPUB reader, or Kindle reader.
545 _aProfessor Glaeser (UC Berkeley) made major contributions to the initial development of cryo-EM technology, and he currently is active in the improvement of specimen preparation. Professor Nogales (UC Berkeley) has used cryo-EM throughout her scientific career, successfully applying this technique for the last three decades to systems that defied structural characterization. Professor Chiu (Stanford University) developed early experimental and computational methods toward 3D structure determination of biomolecules toward atomic resolution.
588 0 _aTitle from PDF title page (viewed on June 11, 2021).
650 0 _aMacromolecules
_xAnalysis.
_970271
650 0 _aBiomolecules
_xAnalysis.
_912076
650 0 _aHigh resolution imaging.
_911219
650 7 _aBiophysics.
_2bicssc
_94093
650 7 _aSCIENCE / Life Sciences / Biophysics.
_2bisacsh
_914896
700 1 _aGlaeser, Robert M.,
_eauthor.
_970272
700 1 _aNogales, Eva,
_eauthor.
_970273
700 1 _aChiu, Wah,
_eauthor.
_970274
710 2 _aInstitute of Physics (Great Britain),
_epublisher.
_911622
776 0 8 _iPrint version:
_z9780750330374
_z9780750330404
830 0 _aIOP (Series).
_pRelease 21.
_970275
830 0 _aBiophysical Society-IOP series.
_970276
830 0 _aIOP ebooks.
_p2021 collection.
_970277
856 4 0 _uhttps://iopscience.iop.org/book/978-0-7503-3039-8
942 _cEBK
999 _c82810
_d82810