2010
DOI: 10.1007/s00425-010-1116-y
|View full text |Cite
|
Sign up to set email alerts
|

Monoclonal antibodies to rhamnogalacturonan I backbone

Abstract: Monoclonal antibodies were raised against rhamnogalacturonan I backbone, a pectin domain, using Arabidopsis thaliana seed mucilage-derived rhamnogalacturonan I oligosaccharides--BSA conjugates. Two monoclonal antibodies, designated INRA-RU1 and INRA-RU2, selected for further characterization, were specific for the backbone of rhamnogalacturonan I, displaying no binding activity against the other pectin domains i.e. homogalacturonans, galactans or arabinans. A range of oligosaccharides was prepared by enzymatic… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

4
97
0

Year Published

2012
2012
2023
2023

Publication Types

Select...
5
2
2

Relationship

0
9

Authors

Journals

citations
Cited by 117 publications
(101 citation statements)
references
References 45 publications
4
97
0
Order By: Relevance
“…INRA-RU1 binds unbranched rhamnogalacturonan I chains (Ralet et al, 2010), while LM21 binds effectively to all HM polymers, regardless of their degree of substitution (Marcus et al, 2010). Wild-type and mutant mucilage showed a similar INRA-RU1 labeling (Fig.…”
Section: Muci10 Is Essential For the Distribution Of Hm In Adherent Mmentioning
confidence: 84%
See 1 more Smart Citation
“…INRA-RU1 binds unbranched rhamnogalacturonan I chains (Ralet et al, 2010), while LM21 binds effectively to all HM polymers, regardless of their degree of substitution (Marcus et al, 2010). Wild-type and mutant mucilage showed a similar INRA-RU1 labeling (Fig.…”
Section: Muci10 Is Essential For the Distribution Of Hm In Adherent Mmentioning
confidence: 84%
“…Whole seeds were immunolabeled as described previously (Macquet et al, 2007) using LM21 (PlantProbes) and INRA-RU1 (Institut National de la Recherche Agronomique) primary antibodies (Marcus et al, 2010;Ralet et al, 2010). Alexa Fluor 488 (Molecular Probes, Life Technologies) was used as a secondary antibody.…”
Section: Immunolabeling Experimentsmentioning
confidence: 99%
“…Same as in flax [42,43], fraction of this polymer is so tightly retained by cellulose that can be obtained only after complete cellulose degradation [38]. The antibody RU2 against rhamnogalacturonan I backbone [44] does not recognize any epitopes within S1 layer, but binds to the thick inner cell wall layers of hemp fibers, both primary and secondary, same as to the primary cell wall/middle lamellae region [38] (Figure 6). Cytochemical staining for pectin is also positive in the inner layers of hemp fibers [6].…”
Section: Cell Wall Thickeningmentioning
confidence: 99%
“…2A). For example, the relative abundances of rhamnogalacturonan I (RGI) backbone epitopes recognized by the mAbs INRA-RUI and INRA-RU2 (Ralet et al, 2010) were reduced by 58% and 68%, respectively, in CDTA fractions, while the relative level of binding of all HG-directed mAbs was reduced by between 32% and 57% ( Fig. 2A).…”
Section: Carbohydrate Microarray Profiling Provides An Overview Of Cementioning
confidence: 99%