Membrane Anchoring of α-Helical Proteins

Role of Tryptophan

Alan J. Situ, So Min Kang, Benjamin B. Frey, Woojin An, Chungho Kim, Tobias S. Ulmer

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The function of membrane proteins relies on a defined orientation of protein relative to lipid. In apparent correlation to protein anchoring, tryptophan residues are enriched in the lipid headgroup region. To characterize the thermodynamic and structural basis of this relationship in α-helical membrane proteins, we examined the role of three conserved tryptophans in the folding of the heterodimeric integrin αIIbβ3 transmembrane (TM) complex in phospholipid bicelles and mammalian membranes. In the homogenous lipid environment of bicelles, tryptophan was replaceable by residues of distinct polarities. The appropriate polarity was guided by the electrostatic potential of the tryptophan surrounding, suggesting that tryptophan can complement diverse environments by adjusting the orientation of its anisotropic side chain to achieve site-specific anchoring. As a sole membrane anchor, tryptophan made a contribution of 0.4 kcal/mol to TM complex stability in bicelles. In membranes, it proved more difficult to replace tryptophan even by tyrosine, indicating a superior capacity to interact with heterogeneous lipids of biological membranes. Interestingly, at intracellular TM helix ends, where integrin activation is initiated, sequence motifs that interact with lipids via opposing polarity patterns were found to restrict TM helix orientations beyond tryptophan anchoring. In contrast to bicelles, phenylalanine became the least accepted substitute in membranes, demonstrating an increased role of the hydrophobic effect. Altogether, our study implicates a wide amphiphilic range of tryptophan, membrane complexity, and the hydrophobic effect to be important factors in tryptophan membrane anchoring.

Original languageEnglish
Pages (from-to)1185-1194
Number of pages10
JournalJournal of Physical Chemistry B
Volume122
Issue number3
DOIs
Publication statusPublished - 2018 Jan 25

Fingerprint

tryptophan
Tryptophan
membranes
proteins
Proteins
Membranes
Lipids
lipids
polarity
Integrins
helices
Biological membranes
Membrane Proteins
Phospholipids
Anchors
phenylalanine
tyrosine
Electrostatics
Membrane Lipids
Static Electricity

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films
  • Materials Chemistry

Cite this

Membrane Anchoring of α-Helical Proteins : Role of Tryptophan. / Situ, Alan J.; Kang, So Min; Frey, Benjamin B.; An, Woojin; Kim, Chungho; Ulmer, Tobias S.

In: Journal of Physical Chemistry B, Vol. 122, No. 3, 25.01.2018, p. 1185-1194.

Research output: Contribution to journalArticle

Situ, Alan J. ; Kang, So Min ; Frey, Benjamin B. ; An, Woojin ; Kim, Chungho ; Ulmer, Tobias S. / Membrane Anchoring of α-Helical Proteins : Role of Tryptophan. In: Journal of Physical Chemistry B. 2018 ; Vol. 122, No. 3. pp. 1185-1194.
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