Elderberry Bark Lectins Evolved to Recognize Neu5Acα2,6Gal/GalNAc Sequence from a Gal/GalNAc Binding Lectin Through the Substitution of Amino-Acid Residues Critical for the Binding to Sialic Acid

Bark lectins from the elderberry plants belonging to the genus Sambucus specifically bind to Neu5Acα2,6Gal/GalNAc sequence and have long been used for the analysis of sialoglycoconjugates that play important roles in many biological phenomena. However, molecular basis of such a unique carbohydrate b...

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Published in:Journal of biochemistry (Tokyo) Vol. 142; no. 3; pp. 393 - 401
Main Authors: Kaku, Hanae, Kaneko, Hiroki, Minamihara, Naoto, Iwata, Kazumichi, Jordan, Elizabeth T., Rojo, Maria A., Minami-Ishii, Naoko, Minami, Eiichi, Hisajima, Shigeru, Shibuya, Naoto
Format: Journal Article
Language:English
Published: Oxford University Press 01-09-2007
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Abstract Bark lectins from the elderberry plants belonging to the genus Sambucus specifically bind to Neu5Acα2,6Gal/GalNAc sequence and have long been used for the analysis of sialoglycoconjugates that play important roles in many biological phenomena. However, molecular basis of such a unique carbohydrate binding specificity has not been understood. To answer these questions, we tried to identify the amino-acid residues in the Japanese elderberry bark lectin, Sambucus sieboldiana agglutinin that enabled the lectin to recognize sialic acid by using in silico docking simulation and site-directed mutagenesis. These studies showed that three amino-acid residues, S197, A233 and Q234, in the C-terminal subdomain of SSA-B chain are critical for the binding to the sialic acid in Neu5Acα2,6Gal/GalNAc sequence. Replacement of one of these residues to the one in the corresponding position of ricin B-chain completely abolished the binding to a sialoglycoprotein, fetuin. Conserved presence of these amino acid residues in the corresponding sequences of two other elderberry lectins with similar binding specificity further supported the conclusion. These findings indicated that the replacement of the corresponding amino-acid residues in a putative Gal/GalNAc-specific ancestral lectin to these amino-acid residues generated the unique Neu5Acα2,6Gal/GalNAc-specific elderberry lectins in the course of molecular evolution.
AbstractList Bark lectins from the elderberry plants belonging to the genus Sambucus specifically bind to Neu5Acα2,6Gal/GalNAc sequence and have long been used for the analysis of sialoglycoconjugates that play important roles in many biological phenomena. However, molecular basis of such a unique carbohydrate binding specificity has not been understood. To answer these questions, we tried to identify the amino-acid residues in the Japanese elderberry bark lectin, Sambucus sieboldiana agglutinin that enabled the lectin to recognize sialic acid by using in silico docking simulation and site-directed mutagenesis. These studies showed that three amino-acid residues, S197, A233 and Q234, in the C-terminal subdomain of SSA-B chain are critical for the binding to the sialic acid in Neu5Acα2,6Gal/GalNAc sequence. Replacement of one of these residues to the one in the corresponding position of ricin B-chain completely abolished the binding to a sialoglycoprotein, fetuin. Conserved presence of these amino acid residues in the corresponding sequences of two other elderberry lectins with similar binding specificity further supported the conclusion. These findings indicated that the replacement of the corresponding amino-acid residues in a putative Gal/GalNAc-specific ancestral lectin to these amino-acid residues generated the unique Neu5Acα2,6Gal/GalNAc-specific elderberry lectins in the course of molecular evolution.
Author Minamihara, Naoto
Minami-Ishii, Naoko
Kaneko, Hiroki
Minami, Eiichi
Iwata, Kazumichi
Shibuya, Naoto
Kaku, Hanae
Hisajima, Shigeru
Jordan, Elizabeth T.
Rojo, Maria A.
Author_xml – sequence: 1
  givenname: Hanae
  surname: Kaku
  fullname: Kaku, Hanae
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
– sequence: 2
  givenname: Hiroki
  surname: Kaneko
  fullname: Kaneko, Hiroki
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
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  givenname: Naoto
  surname: Minamihara
  fullname: Minamihara, Naoto
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
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  givenname: Kazumichi
  surname: Iwata
  fullname: Iwata, Kazumichi
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
– sequence: 5
  givenname: Elizabeth T.
  surname: Jordan
  fullname: Jordan, Elizabeth T.
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
– sequence: 6
  givenname: Maria A.
  surname: Rojo
  fullname: Rojo, Maria A.
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
– sequence: 7
  givenname: Naoko
  surname: Minami-Ishii
  fullname: Minami-Ishii, Naoko
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
– sequence: 8
  givenname: Eiichi
  surname: Minami
  fullname: Minami, Eiichi
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
– sequence: 9
  givenname: Shigeru
  surname: Hisajima
  fullname: Hisajima, Shigeru
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
– sequence: 10
  givenname: Naoto
  surname: Shibuya
  fullname: Shibuya, Naoto
  email: shibuya@isc.meiji.ac.jp, †To whom correspondence should be addressed. Tel: +81-44-934-7039, shibuya@isc.meiji.ac.jp
  organization: Department of Life Sciences, Meiji University, Kawasaki, Kanagawa 214-8571; Department of Integrated Sciences in Physics and Biology, Nihon University, Tokyo 156-8550; Department of Biochemistry, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602; and Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8577, Japan
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Keywords elderberry
sialic acid
lectin
docking simulation
Language English
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Notes The first three authors contributed equally to this work.
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Snippet Bark lectins from the elderberry plants belonging to the genus Sambucus specifically bind to Neu5Acα2,6Gal/GalNAc sequence and have long been used for the...
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StartPage 393
SubjectTerms docking simulation
elderberry
lectin
Sambucus sieboldiana
sialic acid
Title Elderberry Bark Lectins Evolved to Recognize Neu5Acα2,6Gal/GalNAc Sequence from a Gal/GalNAc Binding Lectin Through the Substitution of Amino-Acid Residues Critical for the Binding to Sialic Acid
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