Your browser doesn't support javascript.
loading
High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases.
Schermerhorn, Kelly M; Tanner, Nathan; Kelman, Zvi; Gardner, Andrew F.
Afiliación
  • Schermerhorn KM; New England Biolabs, Ipswich, MA 01938, USA.
  • Tanner N; New England Biolabs, Ipswich, MA 01938, USA tanner@neb.com.
  • Kelman Z; Biomolecular Labeling Laboratory, National Institute of Standards and Technology and Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850, USA.
  • Gardner AF; New England Biolabs, Ipswich, MA 01938, USA gardner@neb.com.
Nucleic Acids Res ; 44(18): 8764-8771, 2016 Oct 14.
Article en En | MEDLINE | ID: mdl-27382065
ABSTRACT
The minichromosome maintenance (MCM) complex is the replicative helicase responsible for unwinding DNA during archaeal and eukaryal genome replication. To mimic long helicase events in the cell, a high-temperature single-molecule assay was designed to quantitatively measure long-range DNA unwinding of individual DNA helicases from the archaeons Methanothermobacter thermautotrophicus (Mth) and Thermococcus sp. 9°N (9°N). Mth encodes a single MCM homolog while 9°N encodes three helicases. 9°N MCM3, the proposed replicative helicase, unwinds DNA at a faster rate compared to 9°N MCM2 and to Mth MCM. However, all three MCM proteins have similar processivities. The implications of these observations for DNA replication in archaea and the differences and similarities among helicases from different microorganisms are discussed. Development of the high-temperature single-molecule assay establishes a system to comprehensively study thermophilic replisomes and evolutionary links between archaeal, eukaryal, and bacterial replication systems.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Termodinámica / ADN Helicasas / Proteínas Arqueales Idioma: En Revista: Nucleic Acids Res Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Termodinámica / ADN Helicasas / Proteínas Arqueales Idioma: En Revista: Nucleic Acids Res Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos