Literature DB >> 23771591

Divide and conquer is always best: sensitivity of methyl correlation experiments.

Kaustubh Sinha1, Linda Jen-Jacobson, Gordon S Rule.   

Abstract

The HMCM [CG]CBCA experiment (Tugarinov and Kay in J Am Chem Soc 125:13868-13878, 2003) correlates methyl carbon and proton shifts to Cγ, Cβ, and Cα resonances for the purpose of resonance assignments. The relative sensitivity of the HMCM[CG]CBCA sequence experiment is compared to a divide-and-conquer approach to assess whether it is best to collect all of the methyl correlations at once, or to perform separate experiments for each correlation. A straightforward analysis shows that the divide-and-conquer approach is intrinsically more sensitive, and should always be used to obtain methyl-Cγ, Cβ, and Cα correlations. The improvement in signal-to-noise associated with separate experiments is illustrated by the detection of methyl-aliphatic correlations in a 65 kDa protein-DNA complex.

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Year:  2013        PMID: 23771591      PMCID: PMC3758368          DOI: 10.1007/s10858-013-9751-9

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  31 in total

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Authors:  G A Mueller; W Y Choy; D Yang; J D Forman-Kay; R A Venters; L E Kay
Journal:  J Mol Biol       Date:  2000-06-30       Impact factor: 5.469

Review 2.  TROSY in NMR studies of the structure and function of large biological macromolecules.

Authors:  César Fernández; Gerhard Wider
Journal:  Curr Opin Struct Biol       Date:  2003-10       Impact factor: 6.809

3.  Ile, Leu, and Val methyl assignments of the 723-residue malate synthase G using a new labeling strategy and novel NMR methods.

Authors:  Vitali Tugarinov; Lewis E Kay
Journal:  J Am Chem Soc       Date:  2003-11-12       Impact factor: 15.419

Review 4.  Use of deuterium labeling in NMR: overcoming a sizeable problem.

Authors:  M Sattler; S W Fesik
Journal:  Structure       Date:  1996-11-15       Impact factor: 5.006

5.  Solution structure of the carboxyl terminus of a human class Mu glutathione S-transferase: NMR assignment strategies in large proteins.

Authors:  S A McCallum; T K Hitchens; G S Rule
Journal:  J Mol Biol       Date:  1999-02-05       Impact factor: 5.469

6.  The NMR structure of the RNA binding domain of E. coli rho factor suggests possible RNA-protein interactions.

Authors:  D M Briercheck; T C Wood; T J Allison; J P Richardson; G S Rule
Journal:  Nat Struct Biol       Date:  1998-05

7.  3D-TROSY-based backbone and ILV-methyl resonance assignments of a 319-residue homodimer from a single protein sample.

Authors:  Anna Krejcirikova; Vitali Tugarinov
Journal:  J Biomol NMR       Date:  2012-09-08       Impact factor: 2.835

8.  A robust and cost-effective method for the production of Val, Leu, Ile (delta 1) methyl-protonated 15N-, 13C-, 2H-labeled proteins.

Authors:  N K Goto; K H Gardner; G A Mueller; R C Willis; L E Kay
Journal:  J Biomol NMR       Date:  1999-04       Impact factor: 2.835

9.  NMR sequential assignment of Escherichia coli thioredoxin utilizing random fractional deuteriation.

Authors:  D M LeMaster; F M Richards
Journal:  Biochemistry       Date:  1988-01-12       Impact factor: 3.162

10.  TROSY in triple-resonance experiments: new perspectives for sequential NMR assignment of large proteins.

Authors:  M Salzmann; K Pervushin; G Wider; H Senn; K Wüthrich
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

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2.  Metal Ion Binding at the Catalytic Site Induces Widely Distributed Changes in a Sequence Specific Protein-DNA Complex.

Authors:  Kaustubh Sinha; Sahil S Sangani; Andrew D Kehr; Gordon S Rule; Linda Jen-Jacobson
Journal:  Biochemistry       Date:  2016-10-27       Impact factor: 3.162

3.  1H, 13C, 15N backbone and IVL methyl group resonance assignment of the fungal β-glucosidase from Trichoderma reesei.

Authors:  Eleni Makraki; Marta G Carneiro; Alex Heyam; A B Eiso; Gregg Siegal; Roderick E Hubbard
Journal:  Biomol NMR Assign       Date:  2020-06-19       Impact factor: 0.746

4.  High-resolution ex vivo NMR spectroscopy of human Z α1-antitrypsin.

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