Binding of human C4BP to the hypervariable region of M protein: a molecular mechanism of phagocytosis resistance in Streptococcus pyogenes
(2001) In Molecular Microbiology 42(2). p.539-551- Abstract
- The amino-terminal hypervariable region (HVR) of streptococcal M protein is required for the ability of this virulence factor to confer phagocytosis resistance. The function of the HVR has remained unknown, but the finding that many HVRs with extremely divergent sequences bind the human complement regulator C4b-binding protein (C4BP) has suggested that this ligand may play a role in phagocytosis resistance. We used the M22 system to study the function of bound C4BP and provide several lines of evidence that C4BP indeed contributes to phagocytosis resistance. First, the ability of anti-HVR antibodies to cause opsonization correlated with their ability to inhibit binding of C4BP. Secondly, a short deletion in the HVR eliminated C4BP binding... (More)
- The amino-terminal hypervariable region (HVR) of streptococcal M protein is required for the ability of this virulence factor to confer phagocytosis resistance. The function of the HVR has remained unknown, but the finding that many HVRs with extremely divergent sequences bind the human complement regulator C4b-binding protein (C4BP) has suggested that this ligand may play a role in phagocytosis resistance. We used the M22 system to study the function of bound C4BP and provide several lines of evidence that C4BP indeed contributes to phagocytosis resistance. First, the ability of anti-HVR antibodies to cause opsonization correlated with their ability to inhibit binding of C4BP. Secondly, a short deletion in the HVR eliminated C4BP binding and also reduced the ability of M22 to confer phagocytosis resistance. Thirdly, the addition of an excess of pure C4BP to a phagocytosis system almost completely blocked the effect of opsonizing anti-HVR antibodies. Together, our data indicate that binding of C4BP to the HVR of M22 plays an important role in phagocytosis resistance, but other properties of M22 also contribute. This study provides the first molecular insight into the mechanisms by which the HVR of an M protein confers phagocytosis resistance. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1118690
- author
- Berggård, Karin LU ; Johnsson, E. LU ; Morfeldt, E. ; Persson, J. LU ; Stålhammar-Carlemalm, Margaretha LU and Lindahl, G.
- organization
- publishing date
- 2001
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Molecular Microbiology
- volume
- 42
- issue
- 2
- pages
- 539 - 551
- publisher
- Wiley-Blackwell
- external identifiers
-
- wos:000172098700021
- scopus:0034768706
- ISSN
- 1365-2958
- DOI
- 10.1046/j.1365-2958.2001.02664.x
- language
- English
- LU publication?
- yes
- id
- 07425b9a-6b9c-4293-b0a7-a5279d162aaa (old id 1118690)
- date added to LUP
- 2016-04-01 12:10:39
- date last changed
- 2022-01-26 23:53:07
@article{07425b9a-6b9c-4293-b0a7-a5279d162aaa,
abstract = {{The amino-terminal hypervariable region (HVR) of streptococcal M protein is required for the ability of this virulence factor to confer phagocytosis resistance. The function of the HVR has remained unknown, but the finding that many HVRs with extremely divergent sequences bind the human complement regulator C4b-binding protein (C4BP) has suggested that this ligand may play a role in phagocytosis resistance. We used the M22 system to study the function of bound C4BP and provide several lines of evidence that C4BP indeed contributes to phagocytosis resistance. First, the ability of anti-HVR antibodies to cause opsonization correlated with their ability to inhibit binding of C4BP. Secondly, a short deletion in the HVR eliminated C4BP binding and also reduced the ability of M22 to confer phagocytosis resistance. Thirdly, the addition of an excess of pure C4BP to a phagocytosis system almost completely blocked the effect of opsonizing anti-HVR antibodies. Together, our data indicate that binding of C4BP to the HVR of M22 plays an important role in phagocytosis resistance, but other properties of M22 also contribute. This study provides the first molecular insight into the mechanisms by which the HVR of an M protein confers phagocytosis resistance.}},
author = {{Berggård, Karin and Johnsson, E. and Morfeldt, E. and Persson, J. and Stålhammar-Carlemalm, Margaretha and Lindahl, G.}},
issn = {{1365-2958}},
language = {{eng}},
number = {{2}},
pages = {{539--551}},
publisher = {{Wiley-Blackwell}},
series = {{Molecular Microbiology}},
title = {{Binding of human C4BP to the hypervariable region of M protein: a molecular mechanism of phagocytosis resistance in Streptococcus pyogenes}},
url = {{http://dx.doi.org/10.1046/j.1365-2958.2001.02664.x}},
doi = {{10.1046/j.1365-2958.2001.02664.x}},
volume = {{42}},
year = {{2001}},
}