Literature DB >> 8953221

Phase labeling of C-H and C-C spin-system topologies: application in constant-time PFG-CBCA(CO)NH experiments for discriminating amino acid spin-system types.

C B Rios1, W Feng, M Tashiro, Z Shang, G T Montelione.   

Abstract

Triple-resonance experiments facilitate the determination of sequence-specific resonance assignments of medium-sized 13C,15N-enriched proteins. Some triple-resonance experiments can also be used to obtain information about amino acid spin-system topologies by proper delay tuning. The constant-time PFG-CBCA(CO)NH experiment allows discrimination between five different groups of amino acids by tuning (phase labeling) independently the delays for proton-carbon refocusing and carbon-carbon constant-time frequency labeling. The proton-carbon refocusing delay allows discrimination of spin-system topologies based on the number of protons attached to C alpha and C beta atoms (i.e. C-H phase labeling). In addition, tuning of the carbon-carbon constant-time frequency-labeling delay discriminates topologies based on the number of carbons directly coupled to C alpha and C beta atoms (i.e. C-C phase labeling). Classifying the spin systems into these five groups facilitates identification of amino acid types, making both manual and automated analysis of assignments easier. The use of this pair of optimally tuned PFG-CBCA(CO)NH experiments for distinguishing five spin-system topologies is demonstrated for the 124-residue bovine pancreatic ribonuclease A protein.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8953221     DOI: 10.1007/bf00410332

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


  17 in total

1.  Structures of larger proteins in solution: three- and four-dimensional heteronuclear NMR spectroscopy.

Authors:  G M Clore; A M Gronenborn
Journal:  Science       Date:  1991-06-07       Impact factor: 47.728

2.  A computer-based protocol for semiautomated assignments and 3D structure determination of proteins.

Authors:  R P Meadows; E T Olejniczak; S W Fesik
Journal:  J Biomol NMR       Date:  1994-01       Impact factor: 2.835

3.  Phase labeling of C-H and C-C spin-system topologies: application in PFG-HACANH and PFG-HACA(CO)NH triple-resonance experiments for determining backbone resonance assignments in proteins.

Authors:  W Feng; C B Rios; G T Montelione
Journal:  J Biomol NMR       Date:  1996-07       Impact factor: 2.835

4.  Two-dimensional nuclear magnetic resonance method for identifying the HN/N signals of amino-acid residues following glycine.

Authors:  K Gehring; E Guittet
Journal:  J Magn Reson B       Date:  1995-11

5.  Amino-acid-type-selective triple-resonance experiments.

Authors:  V Dötsch; R E Oswald; G Wagner
Journal:  J Magn Reson B       Date:  1996-01

Review 6.  Automated analysis of nuclear magnetic resonance assignments for proteins.

Authors:  D E Zimmerman; G T Montelione
Journal:  Curr Opin Struct Biol       Date:  1995-10       Impact factor: 6.809

7.  Automated sequencing of amino acid spin systems in proteins using multidimensional HCC(CO)NH-TOCSY spectroscopy and constraint propagation methods from artificial intelligence.

Authors:  D Zimmerman; C Kulikowski; L Wang; B Lyons; G T Montelione
Journal:  J Biomol NMR       Date:  1994-03       Impact factor: 2.835

8.  Classification of amino acid spin systems using PFG HCC(CO)NH-TOCSY with constant-time aliphatic 13C frequency labeling.

Authors:  M Tashiro; C B Rios; G T Montelione
Journal:  J Biomol NMR       Date:  1995-09       Impact factor: 2.835

9.  An automated procedure for the assignment of protein 1HN, 15N, 13C alpha, 1H alpha, 13C beta and 1H beta resonances.

Authors:  M S Friedrichs; L Mueller; M Wittekind
Journal:  J Biomol NMR       Date:  1994-09       Impact factor: 2.835

10.  A novel approach for sequential assignment of 1H, 13C, and 15N spectra of proteins: heteronuclear triple-resonance three-dimensional NMR spectroscopy. Application to calmodulin.

Authors:  M Ikura; L E Kay; A Bax
Journal:  Biochemistry       Date:  1990-05-15       Impact factor: 3.162

View more
  12 in total

1.  Efficient identification of amino acid types for fast protein backbone assignments.

Authors:  H D Ou; H C Lai; Z Serber; V Dötsch
Journal:  J Biomol NMR       Date:  2001-11       Impact factor: 2.835

2.  Structure and interactions of the carboxyl terminus of striated muscle alpha-tropomyosin: it is important to be flexible.

Authors:  Norma J Greenfield; Thomas Palm; Sarah E Hitchcock-DeGregori
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

3.  Rapid analysis of protein backbone resonance assignments using cryogenic probes, a distributed Linux-based computing architecture, and an integrated set of spectral analysis tools.

Authors:  Daniel Monleón; Kimberly Colson; Hunter N B Moseley; Clemens Anklin; Robert Oswald; Thomas Szyperski; Gaetano T Montelione
Journal:  J Struct Funct Genomics       Date:  2002

4.  Bridge over troubled proline: assignment of intrinsically disordered proteins using (HCA)CON(CAN)H and (HCA)N(CA)CO(N)H experiments concomitantly with HNCO and i(HCA)CO(CA)NH.

Authors:  Maarit Hellman; Henni Piirainen; Veli-Pekka Jaakola; Perttu Permi
Journal:  J Biomol NMR       Date:  2013-12-18       Impact factor: 2.835

5.  Phase labeling of C-H and C-C spin-system topologies: application in PFG-HACANH and PFG-HACA(CO)NH triple-resonance experiments for determining backbone resonance assignments in proteins.

Authors:  W Feng; C B Rios; G T Montelione
Journal:  J Biomol NMR       Date:  1996-07       Impact factor: 2.835

6.  New amino acid residue type identification experiments valid for protonated and deuterated proteins.

Authors:  David Pantoja-Uceda; Jorge Santoro
Journal:  J Biomol NMR       Date:  2012-09-04       Impact factor: 2.835

7.  Editing and diagonal peak suppression in three-dimensional HCCH protein NMR correlation experiments.

Authors:  A Meissner; O W Sørensen
Journal:  J Biomol NMR       Date:  2001-01       Impact factor: 2.835

8.  A Spin System Labeled and Highly Resolved ed-H(CCO)NH-TOCSY Experiment for the Facilitated Assignment of Proton Side Chains in Partially Deuterated Samples.

Authors:  R M Gschwind; G Gemmecker; H Kessler
Journal:  J Biomol NMR       Date:  1998-02       Impact factor: 2.835

9.  Structure of the N terminus of a nonmuscle alpha-tropomyosin in complex with the C terminus: implications for actin binding.

Authors:  Norma J Greenfield; Lucy Kotlyanskaya; Sarah E Hitchcock-DeGregori
Journal:  Biochemistry       Date:  2009-02-17       Impact factor: 3.162

10.  Structure and tropomyosin binding properties of the N-terminal capping domain of tropomodulin 1.

Authors:  Norma J Greenfield; Alla S Kostyukova; Sarah E Hitchcock-DeGregori
Journal:  Biophys J       Date:  2004-10-08       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.