Literature DB >> 11133240

Kinetics: a tool to study molecular motors.

S P Gilbert1, A T Mackey.   

Abstract

Molecular motors are enzymes that couple the energy from nucleoside triphosphate hydrolysis to movement along a filament lattice. The three cytoskeletal motor superfamilies include myosin, dynein, and kinesin. However, in the last decade it has become apparent that the nucleic acid-based enzymes (DNA and RNA polymerases as well as the DNA helicases) share a number of mechanistic features in common with the microtubule and actin motors despite the fact that their cellular functions are so different. This review addresses the mechanistic approaches that have been used to study molecular motors. We discuss the basic biochemical techniques used to characterize a protein preparation, including active site determination and steady-state kinetics. In addition, we present the transient-state kinetic approaches used to define a mechanochemical cycle. We attempt to integrate the information obtained from kinetic studies within the context of motility results to provide a better understanding of the contribution of each approach for dissecting unidirectional force generation. Copyright 2000 Academic Press.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11133240     DOI: 10.1006/meth.2000.1086

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  42 in total

1.  Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair.

Authors:  Edwin Antony; Manju M Hingorani
Journal:  Biochemistry       Date:  2003-07-01       Impact factor: 3.162

2.  A kinesin switch I arginine to lysine mutation rescues microtubule function.

Authors:  Lisa M Klumpp; Andrew T Mackey; Christopher M Farrell; John M Rosenberg; Susan P Gilbert
Journal:  J Biol Chem       Date:  2003-07-14       Impact factor: 5.157

3.  Mechanistic analysis of the Saccharomyces cerevisiae kinesin Kar3.

Authors:  Andrew T Mackey; Lisa R Sproul; Christopher A Sontag; Lisa L Satterwhite; John J Correia; Susan P Gilbert
Journal:  J Biol Chem       Date:  2004-09-21       Impact factor: 5.157

4.  Biochemical characterization of bacteriophage T4 Mre11-Rad50 complex.

Authors:  Timothy J Herdendorf; Dustin W Albrecht; Stephen J Benkovic; Scott W Nelson
Journal:  J Biol Chem       Date:  2010-11-15       Impact factor: 5.157

5.  Analyses of dynein heavy chain mutations reveal complex interactions between dynein motor domains and cellular dynein functions.

Authors:  Senthilkumar Sivagurunathan; Robert R Schnittker; David S Razafsky; Swaran Nandini; Michael D Plamann; Stephen J King
Journal:  Genetics       Date:  2012-05-29       Impact factor: 4.562

6.  Analysis of the DNA translocation and unwinding activities of T4 phage helicases.

Authors:  Senthil K Perumal; Kevin D Raney; Stephen J Benkovic
Journal:  Methods       Date:  2010-02-17       Impact factor: 3.608

7.  Identification of the proteasome inhibitor MG262 as a potent ATP-dependent inhibitor of the Salmonella enterica serovar Typhimurium Lon protease.

Authors:  Hilary Frase; Jason Hudak; Irene Lee
Journal:  Biochemistry       Date:  2006-07-11       Impact factor: 3.162

8.  Single-turnover kinetic experiments confirm the existence of high- and low-affinity ATPase sites in Escherichia coli Lon protease.

Authors:  Diana Vineyard; Jessica Patterson-Ward; Irene Lee
Journal:  Biochemistry       Date:  2006-04-11       Impact factor: 3.162

9.  Dimeric Eg5 maintains processivity through alternating-site catalysis with rate-limiting ATP hydrolysis.

Authors:  Troy C Krzysiak; Susan P Gilbert
Journal:  J Biol Chem       Date:  2006-10-23       Impact factor: 5.157

10.  Recognition of a Key Anchor Residue by a Conserved Hydrophobic Pocket Ensures Subunit Interface Integrity in DNA Clamps.

Authors:  Senthil K Perumal; Xiaojun Xu; Chunli Yan; Ivaylo Ivanov; Stephen J Benkovic
Journal:  J Mol Biol       Date:  2019-04-30       Impact factor: 5.469

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.