A unique phenylalanine in the transmembrane domain strengthens homodimerization of the syndecan-2 Transmembrane Domain and Functionally Regulates Syndecan-2

Mi Jung Kwon, Youngsil Choi, Ji Hye Yun, Weon Tae Lee, Inn Oc Han, Eok Soo Oh

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The syndecans are a type of cell surface adhesion receptor that initiates intracellular signaling events through receptor clustering mediated by their highly conserved transmembrane domains (TMDs). However, the exact function of the syndecan TMD is not yet fully understood. Here, we investigated the specific regulatory role of the syndecan-2 TMD.Wefound that syn-decan-2 mutants in which theTMDhad been replaced with that of syndecan-4 were defective in syndecan-2-mediated functions, suggesting that theTMDof syndecan-2 plays one or more specific roles. Interestingly, syndecan-2 has a stronger tendency to form sodium dodecyl sulfate (SDS)-resistant homodimers than syndecan-4. Our structural studies showed that a unique phenylalanine residue (Phe167) enables an additional molecular interaction between the TMDs of the syndecan-2 homodimer. The presence of Phe167 was correlated with a higher tendency toward oligomerization, and its replacement with isoleucine significantly reduced the SDS-resistant dimer formation and cellular functions of syndecan-2 (e.g. cell migration). Conversely, replacement of isoleucine with phenylalanine at this position in the syndecan-4TMDrescued the defects observed in a mutant syndecan-2 harboring the syndecan-4 TMD. Taken together, these data suggest that Phe167 in the TMD of synde-can-2 endows the protein with specific functions. Our work offers new insights into the signaling mediated by the TMD of syndecan family members.

Original languageEnglish
Pages (from-to)5772-5782
Number of pages11
JournalJournal of Biological Chemistry
Volume290
Issue number9
DOIs
Publication statusPublished - 2015 Feb 27

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Syndecan-2
Phenylalanine
Syndecans
Syndecan-4
Isoleucine
Sodium Dodecyl Sulfate
Oligomerization
Molecular interactions
Cell Surface Receptors
Cell Adhesion
Dimers
Cell Movement
Cluster Analysis
Defects

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

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title = "A unique phenylalanine in the transmembrane domain strengthens homodimerization of the syndecan-2 Transmembrane Domain and Functionally Regulates Syndecan-2",
abstract = "The syndecans are a type of cell surface adhesion receptor that initiates intracellular signaling events through receptor clustering mediated by their highly conserved transmembrane domains (TMDs). However, the exact function of the syndecan TMD is not yet fully understood. Here, we investigated the specific regulatory role of the syndecan-2 TMD.Wefound that syn-decan-2 mutants in which theTMDhad been replaced with that of syndecan-4 were defective in syndecan-2-mediated functions, suggesting that theTMDof syndecan-2 plays one or more specific roles. Interestingly, syndecan-2 has a stronger tendency to form sodium dodecyl sulfate (SDS)-resistant homodimers than syndecan-4. Our structural studies showed that a unique phenylalanine residue (Phe167) enables an additional molecular interaction between the TMDs of the syndecan-2 homodimer. The presence of Phe167 was correlated with a higher tendency toward oligomerization, and its replacement with isoleucine significantly reduced the SDS-resistant dimer formation and cellular functions of syndecan-2 (e.g. cell migration). Conversely, replacement of isoleucine with phenylalanine at this position in the syndecan-4TMDrescued the defects observed in a mutant syndecan-2 harboring the syndecan-4 TMD. Taken together, these data suggest that Phe167 in the TMD of synde-can-2 endows the protein with specific functions. Our work offers new insights into the signaling mediated by the TMD of syndecan family members.",
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A unique phenylalanine in the transmembrane domain strengthens homodimerization of the syndecan-2 Transmembrane Domain and Functionally Regulates Syndecan-2. / Kwon, Mi Jung; Choi, Youngsil; Yun, Ji Hye; Lee, Weon Tae; Han, Inn Oc; Oh, Eok Soo.

In: Journal of Biological Chemistry, Vol. 290, No. 9, 27.02.2015, p. 5772-5782.

Research output: Contribution to journalArticle

TY - JOUR

T1 - A unique phenylalanine in the transmembrane domain strengthens homodimerization of the syndecan-2 Transmembrane Domain and Functionally Regulates Syndecan-2

AU - Kwon, Mi Jung

AU - Choi, Youngsil

AU - Yun, Ji Hye

AU - Lee, Weon Tae

AU - Han, Inn Oc

AU - Oh, Eok Soo

PY - 2015/2/27

Y1 - 2015/2/27

N2 - The syndecans are a type of cell surface adhesion receptor that initiates intracellular signaling events through receptor clustering mediated by their highly conserved transmembrane domains (TMDs). However, the exact function of the syndecan TMD is not yet fully understood. Here, we investigated the specific regulatory role of the syndecan-2 TMD.Wefound that syn-decan-2 mutants in which theTMDhad been replaced with that of syndecan-4 were defective in syndecan-2-mediated functions, suggesting that theTMDof syndecan-2 plays one or more specific roles. Interestingly, syndecan-2 has a stronger tendency to form sodium dodecyl sulfate (SDS)-resistant homodimers than syndecan-4. Our structural studies showed that a unique phenylalanine residue (Phe167) enables an additional molecular interaction between the TMDs of the syndecan-2 homodimer. The presence of Phe167 was correlated with a higher tendency toward oligomerization, and its replacement with isoleucine significantly reduced the SDS-resistant dimer formation and cellular functions of syndecan-2 (e.g. cell migration). Conversely, replacement of isoleucine with phenylalanine at this position in the syndecan-4TMDrescued the defects observed in a mutant syndecan-2 harboring the syndecan-4 TMD. Taken together, these data suggest that Phe167 in the TMD of synde-can-2 endows the protein with specific functions. Our work offers new insights into the signaling mediated by the TMD of syndecan family members.

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