Major intrinsic polypeptide (MIP26K) from human lens membrane: Characterization of low-molecular-weight forms in the aging human lens

L. Takemoto, M. Takehana

研究成果: Article査読

25 被引用数 (Scopus)

抄録

Antisera made against a C-terminal octapeptide of bovine MIP26K and against an N-terminal nonapeptide from the same protein have been used to determine the location of age-dependent cleavage sites of MIP26K in the human lens. Neither the C-terminal antiserum (anti-MIP26K256-263) nor the N-terminal antiserum (anti-MIP26K1-9) binds to the 22000 MW form of MIP26K, suggesting cleavage from both the N- and C-terminus during lens aging. Anti-MIP26K256-263, but not anti-MIP26K1-9, binds to 20000 and 15000 MW forms of MIP26K, demonstrating that age-dependent production of these forms occurs by cleavage from the N-terminal side of the molecule. Together, these results show that age-dependent processing of MIP26K in the human lens occurs from both ends of the molecule, with cleavage from the N-terminal end being mainly responsible for production of the lower-molecular-weight 20000 and 15000 MW components.

本文言語English
ページ(範囲)661-667
ページ数7
ジャーナルExperimental Eye Research
43
4
DOI
出版ステータスPublished - 1986 10

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience

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