4.8 Article

Quantitative description of a contractile macromolecular machine

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SCIENCE ADVANCES
卷 7, 期 24, 页码 -

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.abf9601

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资金

  1. UTMB Department of Biochemistry and Molecular Biology
  2. NIGMS [R01 GM139034]
  3. NIH NCCIH [DP1AT010874]
  4. Robert A. Welch Foundation [H-0013]
  5. Sealy Center for Structural Biology and Molecular Biophysics

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By combining structural information, thermodynamic and force spectroscopy analyses, and an original modeling procedure, this study describes the mechanism of pyocin contraction, showing the activation energy, heat release, and force development of the nanomachine.
Contractile injection systems (CISs) [type VI secretion system (T6SS), phage tails, and tailocins] use a contractile sheath-rigid tube machinery to breach cell walls and lipid membranes. The structures of the pre- and postcontraction states of several CISs are known, but the mechanism of contraction remains poorly understood. Combining structural information of the end states of the 12-megadalton R-type pyocin sheath-tube complex with thermodynamic and force spectroscopy analyses and an original modeling procedure, we describe the mechanism of pyocin contraction. We show that this nanomachine has an activation energy of 160 kilocalories/mole (kcal/mol), and it releases 2160 kcal/ mol of heat and develops a force greater than 500 piconewtons. Our combined approach provides a quantitative and experimental description of the membrane penetration process by a CIS.

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