Functional characterization of cardiac actin mutants causing hypertrophic (p.A295S) and dilated cardiomyopathy (p.R312H and p.E361G)

Human wild type (wt) cardiac α-actin and its mutants p.A295S or p.R312H and p.E361G correlated with hypertrophic or dilated cardiomyopathy, respectively, were expressed by using the baculovirus/Sf21 insect cell system. The c-actin variants inhibited DNase I, indicating maintenance of their native st...

Full description

Saved in:
Bibliographic Details
Main Authors: Hassoun, Roua (Author) , Erdmann, Constanze (Author) , Schmitt, Sebastian (Author) , Fujita-Becker, Setsuko (Author) , Mügge, Andreas (Author) , Schröder, Rasmus R. (Author) , Geyer, Matthias (Author) , Borbor, Mina (Author) , Jaquet, Kornelia (Author) , Hamdani, Nazha (Author) , Mannherz, Hans Georg (Author)
Format: Article (Journal)
Language:English
Published: 18 April 2022
In: International journal of molecular sciences
Year: 2022, Volume: 23, Issue: 8, Pages: 1-27
ISSN:1422-0067
DOI:10.3390/ijms23084465
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/ijms23084465
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/1422-0067/23/8/4465
Get full text
Author Notes:Roua Hassoun, Constanze Erdmann, Sebastian Schmitt, Setsuko Fujita-Becker, Andreas Mügge, Rasmus R. Schröder, Matthias Geyer, Mina Borbor, Kornelia Jaquet, Nazha Hamdani and Hans Georg Mannherz

MARC

LEADER 00000caa a2200000 c 4500
001 1810077508
003 DE-627
005 20220820222437.0
007 cr uuu---uuuuu
008 220713s2022 xx |||||o 00| ||eng c
024 7 |a 10.3390/ijms23084465  |2 doi 
035 |a (DE-627)1810077508 
035 |a (DE-599)KXP1810077508 
035 |a (OCoLC)1341463932 
040 |a DE-627  |b ger  |c DE-627  |e rda 
041 |a eng 
084 |a 32  |2 sdnb 
100 1 |a Hassoun, Roua  |e VerfasserIn  |0 (DE-588)1232035920  |0 (DE-627)1755755945  |4 aut 
245 1 0 |a Functional characterization of cardiac actin mutants causing hypertrophic (p.A295S) and dilated cardiomyopathy (p.R312H and p.E361G)  |c Roua Hassoun, Constanze Erdmann, Sebastian Schmitt, Setsuko Fujita-Becker, Andreas Mügge, Rasmus R. Schröder, Matthias Geyer, Mina Borbor, Kornelia Jaquet, Nazha Hamdani and Hans Georg Mannherz 
264 1 |c 18 April 2022 
300 |a 27 
336 |a Text  |b txt  |2 rdacontent 
337 |a Computermedien  |b c  |2 rdamedia 
338 |a Online-Ressource  |b cr  |2 rdacarrier 
500 |a This article belongs to the Section Molecular Biology 
500 |a Gesehen am 13.07.2022 
520 |a Human wild type (wt) cardiac α-actin and its mutants p.A295S or p.R312H and p.E361G correlated with hypertrophic or dilated cardiomyopathy, respectively, were expressed by using the baculovirus/Sf21 insect cell system. The c-actin variants inhibited DNase I, indicating maintenance of their native state. Electron microscopy showed the formation of normal appearing actin filaments though they showed mutant specific differences in length and straightness correlating with their polymerization rates. TRITC-phalloidin staining showed that p.A295S and p.R312H exhibited reduced and the p.E361G mutant increased lengths of their formed filaments. Decoration of c-actins with cardiac tropomyosin (cTm) and troponin (cTn) conveyed Ca2+-sensitivity of the myosin-S1 ATPase stimulation, which was higher for the HCM p.A295S mutant and lower for the DCM p.R312H and p.E361G mutants than for wt c-actin. The lower Ca2+-sensitivity of myosin-S1 stimulation by both DCM actin mutants was corrected by the addition of levosimendan. Ca2+-dependency of the movement of pyrene-labeled cTm along polymerized c-actin variants decorated with cTn corresponded to the relations observed for the myosin-S1 ATPase stimulation though shifted to lower Ca2+-concentrations. The N-terminal C0C2 domain of cardiac myosin-binding protein-C increased the Ca2+-sensitivity of the pyrene-cTM movement of bovine, recombinant wt, p.A295S, and p.E361G c-actins, but not of the p.R312H mutant, suggesting decreased affinity to cTm. 
650 4 |a calcium sensitivity 
650 4 |a cardiac actin 
650 4 |a cardiomyopathies 
650 4 |a levosimendan 
650 4 |a myosin binding protein C 
650 4 |a myosin subfragment 1 
700 1 |a Erdmann, Constanze  |e VerfasserIn  |4 aut 
700 1 |a Schmitt, Sebastian  |e VerfasserIn  |4 aut 
700 1 |a Fujita-Becker, Setsuko  |e VerfasserIn  |0 (DE-588)1204934355  |0 (DE-627)1690220813  |4 aut 
700 1 |a Mügge, Andreas  |d 1956-  |e VerfasserIn  |0 (DE-588)142296287  |0 (DE-627)704193469  |0 (DE-576)329991353  |4 aut 
700 1 |a Schröder, Rasmus R.  |e VerfasserIn  |0 (DE-588)1070886483  |0 (DE-627)824718895  |0 (DE-576)165430702  |4 aut 
700 1 |a Geyer, Matthias  |e VerfasserIn  |4 aut 
700 1 |a Borbor, Mina  |e VerfasserIn  |4 aut 
700 1 |a Jaquet, Kornelia  |e VerfasserIn  |4 aut 
700 1 |a Hamdani, Nazha  |e VerfasserIn  |4 aut 
700 1 |a Mannherz, Hans Georg  |d 1943-  |e VerfasserIn  |0 (DE-588)107223503  |0 (DE-627)690957777  |0 (DE-576)345728114  |4 aut 
773 0 8 |i Enthalten in  |t International journal of molecular sciences  |d Basel : Molecular Diversity Preservation International, 2000  |g 23(2022), 8, Artikel-ID 4465, Seite 1-27  |h Online-Ressource  |w (DE-627)316340715  |w (DE-600)2019364-6  |w (DE-576)281194653  |x 1422-0067  |7 nnas  |a Functional characterization of cardiac actin mutants causing hypertrophic (p.A295S) and dilated cardiomyopathy (p.R312H and p.E361G) 
773 1 8 |g volume:23  |g year:2022  |g number:8  |g month:4-  |g elocationid:4465  |g pages:1-27  |g extent:27  |a Functional characterization of cardiac actin mutants causing hypertrophic (p.A295S) and dilated cardiomyopathy (p.R312H and p.E361G) 
856 4 0 |u https://doi.org/10.3390/ijms23084465  |x Verlag  |x Resolving-System  |z lizenzpflichtig  |3 Volltext 
856 4 0 |u https://www.mdpi.com/1422-0067/23/8/4465  |x Verlag  |z lizenzpflichtig  |3 Volltext 
951 |a AR 
992 |a 20220713 
993 |a Article 
994 |a 2022 
998 |g 1070886483  |a Schröder, Rasmus R.  |m 1070886483:Schröder, Rasmus R.  |d 910000  |d 911700  |d 700000  |d 716000  |e 910000PS1070886483  |e 911700PS1070886483  |e 700000PS1070886483  |e 716000PS1070886483  |k 0/910000/  |k 1/910000/911700/  |k 0/700000/  |k 1/700000/716000/  |p 6 
998 |g 1204934355  |a Fujita-Becker, Setsuko  |m 1204934355:Fujita-Becker, Setsuko  |d 910000  |d 911700  |d 700000  |d 716000  |e 910000PF1204934355  |e 911700PF1204934355  |e 700000PF1204934355  |e 716000PF1204934355  |k 0/910000/  |k 1/910000/911700/  |k 0/700000/  |k 1/700000/716000/  |p 4 
999 |a KXP-PPN1810077508  |e 4165031496 
BIB |a Y 
SER |a journal 
JSO |a {"origin":[{"dateIssuedKey":"2022","dateIssuedDisp":"18 April 2022"}],"recId":"1810077508","name":{"displayForm":["Roua Hassoun, Constanze Erdmann, Sebastian Schmitt, Setsuko Fujita-Becker, Andreas Mügge, Rasmus R. Schröder, Matthias Geyer, Mina Borbor, Kornelia Jaquet, Nazha Hamdani and Hans Georg Mannherz"]},"note":["This article belongs to the Section Molecular Biology","Gesehen am 13.07.2022"],"id":{"doi":["10.3390/ijms23084465"],"eki":["1810077508"]},"type":{"media":"Online-Ressource","bibl":"article-journal"},"physDesc":[{"extent":"27 S."}],"relHost":[{"physDesc":[{"extent":"Online-Ressource"}],"title":[{"title_sort":"International journal of molecular sciences","title":"International journal of molecular sciences"}],"language":["eng"],"note":["Gesehen am 17.09.20"],"disp":"Functional characterization of cardiac actin mutants causing hypertrophic (p.A295S) and dilated cardiomyopathy (p.R312H and p.E361G)International journal of molecular sciences","id":{"zdb":["2019364-6"],"issn":["1422-0067","1661-6596"],"eki":["316340715"]},"type":{"bibl":"periodical","media":"Online-Ressource"},"pubHistory":["1.2000 -"],"part":{"volume":"23","year":"2022","extent":"27","issue":"8","pages":"1-27","text":"23(2022), 8, Artikel-ID 4465, Seite 1-27"},"origin":[{"dateIssuedDisp":"2000-","publisher":"Molecular Diversity Preservation International","dateIssuedKey":"2000","publisherPlace":"Basel"}],"recId":"316340715","titleAlt":[{"title":"IJMS"}]}],"title":[{"title_sort":"Functional characterization of cardiac actin mutants causing hypertrophic (p.A295S) and dilated cardiomyopathy (p.R312H and p.E361G)","title":"Functional characterization of cardiac actin mutants causing hypertrophic (p.A295S) and dilated cardiomyopathy (p.R312H and p.E361G)"}],"person":[{"given":"Roua","family":"Hassoun","role":"aut","display":"Hassoun, Roua"},{"given":"Constanze","family":"Erdmann","role":"aut","display":"Erdmann, Constanze"},{"display":"Schmitt, Sebastian","role":"aut","family":"Schmitt","given":"Sebastian"},{"role":"aut","display":"Fujita-Becker, Setsuko","given":"Setsuko","family":"Fujita-Becker"},{"family":"Mügge","given":"Andreas","display":"Mügge, Andreas","role":"aut"},{"role":"aut","display":"Schröder, Rasmus R.","given":"Rasmus R.","family":"Schröder"},{"family":"Geyer","given":"Matthias","display":"Geyer, Matthias","role":"aut"},{"display":"Borbor, Mina","role":"aut","family":"Borbor","given":"Mina"},{"display":"Jaquet, Kornelia","role":"aut","family":"Jaquet","given":"Kornelia"},{"given":"Nazha","family":"Hamdani","role":"aut","display":"Hamdani, Nazha"},{"given":"Hans Georg","family":"Mannherz","role":"aut","display":"Mannherz, Hans Georg"}],"language":["eng"]} 
SRT |a HASSOUNROUFUNCTIONAL1820