Exploring subdomain cooperativity in T4 lysozyme I: Structural and energetic studies of a circular permutant and protein fragment

Jason Cellitti, Manuel Llinas, Nathaniel Echols, Elizabeth A. Shank, Blake Gillespie, Ester Kwon, Scott M. Crowder, Frederick W. Dahlquist, Tom Alber, Susan Marqusee

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Small proteins are generally observed to fold in an apparent two-state manner. Recently, however, more sensitive techniques have demonstrated that even seemingly single-domain proteins are actually made up of smaller subdomains. T4 lysozyme is one such protein. We explored the relative autonomy of its two individual subdomains and their contribution to the overall stability of T4 lysozyme by examining a circular permutation (CP13*) that relocates the N-terminal A-helix, creating subdomains that are contiguous in sequence. By determining the high-resolution structure of CP13* and characterizing its energy landscape using native state hydrogen exchange (NSHX), we show that connectivity between the subdomains is an important determinant of the energetic cooperativity but not structural integrity of the protein. The circular permutation results in a protein more easily able to populate a partially unfolded form in which the C-terminal subdomain is folded and the N-terminal subdomain is unfolded. We also created a fragment model of this intermediate and demonstrate using X-ray crystallography that its structure is identical to the corresponding residues in the full-length protein with the exception of a small network of hydrophobic interactions. In sum, we conclude that the C-terminal subdomain dominates the energetics of T4 lysozyme folding, and the A-helix serves an important role in coupling the two subdomains. Published by Cold Spring Harbor Laboratory Press.

Original languageEnglish (US)
Pages (from-to)842-851
Number of pages10
JournalProtein Science
Volume16
Issue number5
DOIs
StatePublished - May 1 2007

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Muramidase
Proteins
X Ray Crystallography
Hydrophobic and Hydrophilic Interactions
X ray crystallography
Structural integrity
Ports and harbors
Hydrogen

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology

Cite this

Cellitti, Jason ; Llinas, Manuel ; Echols, Nathaniel ; Shank, Elizabeth A. ; Gillespie, Blake ; Kwon, Ester ; Crowder, Scott M. ; Dahlquist, Frederick W. ; Alber, Tom ; Marqusee, Susan. / Exploring subdomain cooperativity in T4 lysozyme I : Structural and energetic studies of a circular permutant and protein fragment. In: Protein Science. 2007 ; Vol. 16, No. 5. pp. 842-851.
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Cellitti, J, Llinas, M, Echols, N, Shank, EA, Gillespie, B, Kwon, E, Crowder, SM, Dahlquist, FW, Alber, T & Marqusee, S 2007, 'Exploring subdomain cooperativity in T4 lysozyme I: Structural and energetic studies of a circular permutant and protein fragment', Protein Science, vol. 16, no. 5, pp. 842-851. https://doi.org/10.1110/ps.062628607

Exploring subdomain cooperativity in T4 lysozyme I : Structural and energetic studies of a circular permutant and protein fragment. / Cellitti, Jason; Llinas, Manuel; Echols, Nathaniel; Shank, Elizabeth A.; Gillespie, Blake; Kwon, Ester; Crowder, Scott M.; Dahlquist, Frederick W.; Alber, Tom; Marqusee, Susan.

In: Protein Science, Vol. 16, No. 5, 01.05.2007, p. 842-851.

Research output: Contribution to journalArticle

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AU - Echols, Nathaniel

AU - Shank, Elizabeth A.

AU - Gillespie, Blake

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AU - Crowder, Scott M.

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