Mechanochemical Coupling in the Relaxation of Rigor-Wave Sea Urchin Sperm Flagella

The relaxation (straightening) of flagellar rigor waves, which is known to be induced by micromolar ATP concentrations, was investigated with respect to its dependence on the binding and hydrolysis of ATP. Flagellar rigor waves were formed by the dilution of demembranated, reactivated sea urchin (Ly...

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Veröffentlicht in:The Journal of cell biology 1982-03, Vol.92 (3), p.733-741
Hauptverfasser: Penningroth, Stephen M., Cheung, Anne, Olehnik, Kevin, Koslosky, Robert
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container_title The Journal of cell biology
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creator Penningroth, Stephen M.
Cheung, Anne
Olehnik, Kevin
Koslosky, Robert
description The relaxation (straightening) of flagellar rigor waves, which is known to be induced by micromolar ATP concentrations, was investigated with respect to its dependence on the binding and hydrolysis of ATP. Flagellar rigor waves were formed by the dilution of demembranated, reactivated sea urchin (Lytechinus pictus) spermatozoa into ATP-free buffer. Relaxation in response to nucleotide was quantitated by measuring$\%\overline{\Theta}$, the mean flagellar bend angle per sperm; this novel assay permitted determination of the rate of relaxation. It was found that (a) the rate of flagellar relaxation induced by 4× 10-6M ATP was inhibited 80% by vanadate concentrations of 3× 10-5M and above; (b) of 16 hydrolyzable and nonhydrolyzable nucleotide di-, tri-, and tetraphosphates tested, only three, each of which was hydrolyzed by the flagellar axonemal ATPase activity (ATP, dATP, and ε-ATP), were also capable of effecting relaxation; (c) several hundred ATP molecules were estimated to be hydrolyzed by each dynein arm in the course of flagellar relaxation; and (d) the ratio of the rate of relaxation to the rate of ATP hydrolysis, which defines the efficiency of ATP utilization, increased 30-fold as the ATP concentration was raised from 2× 10-6to 9× 10-6M. It is concluded that (a) flagellar relaxation depends on ATP hydrolysis; (b) because it depends on ATP hydrolysis, flagellar relaxation is an inappropriate model system for investigating the role of ATP binding in the mechanochemical cycle of dynein; and (c) the efficiency of mechanochemical coupling in flagellar motility is an ATP-dependent phenomenon. A general model of relaxation is proposed based on active microtubule sliding.
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Flagellar rigor waves were formed by the dilution of demembranated, reactivated sea urchin (Lytechinus pictus) spermatozoa into ATP-free buffer. Relaxation in response to nucleotide was quantitated by measuring$\%\overline{\Theta}$, the mean flagellar bend angle per sperm; this novel assay permitted determination of the rate of relaxation. It was found that (a) the rate of flagellar relaxation induced by 4× 10-6M ATP was inhibited 80% by vanadate concentrations of 3× 10-5M and above; (b) of 16 hydrolyzable and nonhydrolyzable nucleotide di-, tri-, and tetraphosphates tested, only three, each of which was hydrolyzed by the flagellar axonemal ATPase activity (ATP, dATP, and ε-ATP), were also capable of effecting relaxation; (c) several hundred ATP molecules were estimated to be hydrolyzed by each dynein arm in the course of flagellar relaxation; and (d) the ratio of the rate of relaxation to the rate of ATP hydrolysis, which defines the efficiency of ATP utilization, increased 30-fold as the ATP concentration was raised from 2× 10-6to 9× 10-6M. It is concluded that (a) flagellar relaxation depends on ATP hydrolysis; (b) because it depends on ATP hydrolysis, flagellar relaxation is an inappropriate model system for investigating the role of ATP binding in the mechanochemical cycle of dynein; and (c) the efficiency of mechanochemical coupling in flagellar motility is an ATP-dependent phenomenon. 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Flagellar rigor waves were formed by the dilution of demembranated, reactivated sea urchin (Lytechinus pictus) spermatozoa into ATP-free buffer. Relaxation in response to nucleotide was quantitated by measuring$\%\overline{\Theta}$, the mean flagellar bend angle per sperm; this novel assay permitted determination of the rate of relaxation. 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A general model of relaxation is proposed based on active microtubule sliding.</description><subject>Adenine Nucleotides - pharmacology</subject><subject>Adenosine triphosphatases</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Adenosine Triphosphate - metabolism</subject><subject>Animals</subject><subject>Chromatography</subject><subject>Dyneins - metabolism</subject><subject>Flagella</subject><subject>Hydrolysis</subject><subject>Kinetics</subject><subject>Male</subject><subject>Microtubules</subject><subject>Microtubules - enzymology</subject><subject>Molecules</subject><subject>Nucleotides</subject><subject>Nucleotides - metabolism</subject><subject>Sea Urchins - physiology</subject><subject>Sliding</subject><subject>Sperm Tail - physiology</subject><subject>Spermatozoa</subject><subject>Spermatozoa - physiology</subject><subject>Structure-Activity Relationship</subject><subject>Vanadates</subject><subject>Vanadium - pharmacology</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1rGzEQxUVJcJ20tx5b0CmnrDtaabW7l0Aw-QKXgtPQo5DkWa_M7sqV1iH976Ng4zanObwfb-bNI-QLgxmDin_fWDOr8xmflZx_IFNWCMgqJuCETAFyltVFXnwkZzFuAECUgk_IROaMiaKakuUPtK0evG2xd1Z3dO53284Na-oGOrZIl9jpFz06P1Df0KVb-5D91s9IH1HTp2DbxD1uMfT0ttNr7Dr9iZw2uov4-TDPydPtza_5fbb4efcwv15kVkg5ZoI1QldWlGjqxpYFmAJExXIAYyXmJXJpAApruMDa8BS1EpzrpjYraRrW8HNytffd7kyPK4vDGHSntsH1OvxVXjv1Xhlcq9b-WaXsOfAqGVwcDIL_s8M4qt5F-xZhQL-LqhRQQ8FFAi_3oA0-xoDNcQkD9daBSh2oOldcpQ4S_u3_w47w4elJ_7rXN3H04Z-XhLqUkr8C4d-Maw</recordid><startdate>19820301</startdate><enddate>19820301</enddate><creator>Penningroth, Stephen M.</creator><creator>Cheung, Anne</creator><creator>Olehnik, Kevin</creator><creator>Koslosky, Robert</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19820301</creationdate><title>Mechanochemical Coupling in the Relaxation of Rigor-Wave Sea Urchin Sperm Flagella</title><author>Penningroth, Stephen M. ; Cheung, Anne ; Olehnik, Kevin ; Koslosky, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-41f4a8c47eb9fc750b50481200bc6e27e36b005cb34e9b31088433af9bd6bf1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Adenine Nucleotides - pharmacology</topic><topic>Adenosine triphosphatases</topic><topic>Adenosine Triphosphatases - metabolism</topic><topic>Adenosine Triphosphate - metabolism</topic><topic>Animals</topic><topic>Chromatography</topic><topic>Dyneins - metabolism</topic><topic>Flagella</topic><topic>Hydrolysis</topic><topic>Kinetics</topic><topic>Male</topic><topic>Microtubules</topic><topic>Microtubules - enzymology</topic><topic>Molecules</topic><topic>Nucleotides</topic><topic>Nucleotides - metabolism</topic><topic>Sea Urchins - physiology</topic><topic>Sliding</topic><topic>Sperm Tail - physiology</topic><topic>Spermatozoa</topic><topic>Spermatozoa - physiology</topic><topic>Structure-Activity Relationship</topic><topic>Vanadates</topic><topic>Vanadium - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Penningroth, Stephen M.</creatorcontrib><creatorcontrib>Cheung, Anne</creatorcontrib><creatorcontrib>Olehnik, Kevin</creatorcontrib><creatorcontrib>Koslosky, Robert</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Penningroth, Stephen M.</au><au>Cheung, Anne</au><au>Olehnik, Kevin</au><au>Koslosky, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanochemical Coupling in the Relaxation of Rigor-Wave Sea Urchin Sperm Flagella</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>1982-03-01</date><risdate>1982</risdate><volume>92</volume><issue>3</issue><spage>733</spage><epage>741</epage><pages>733-741</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><abstract>The relaxation (straightening) of flagellar rigor waves, which is known to be induced by micromolar ATP concentrations, was investigated with respect to its dependence on the binding and hydrolysis of ATP. 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It was found that (a) the rate of flagellar relaxation induced by 4× 10-6M ATP was inhibited 80% by vanadate concentrations of 3× 10-5M and above; (b) of 16 hydrolyzable and nonhydrolyzable nucleotide di-, tri-, and tetraphosphates tested, only three, each of which was hydrolyzed by the flagellar axonemal ATPase activity (ATP, dATP, and ε-ATP), were also capable of effecting relaxation; (c) several hundred ATP molecules were estimated to be hydrolyzed by each dynein arm in the course of flagellar relaxation; and (d) the ratio of the rate of relaxation to the rate of ATP hydrolysis, which defines the efficiency of ATP utilization, increased 30-fold as the ATP concentration was raised from 2× 10-6to 9× 10-6M. It is concluded that (a) flagellar relaxation depends on ATP hydrolysis; (b) because it depends on ATP hydrolysis, flagellar relaxation is an inappropriate model system for investigating the role of ATP binding in the mechanochemical cycle of dynein; and (c) the efficiency of mechanochemical coupling in flagellar motility is an ATP-dependent phenomenon. A general model of relaxation is proposed based on active microtubule sliding.</abstract><cop>United States</cop><pub>Rockefeller University Press</pub><pmid>6211458</pmid><doi>10.1083/jcb.92.3.733</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenine Nucleotides - pharmacology
Adenosine triphosphatases
Adenosine Triphosphatases - metabolism
Adenosine Triphosphate - metabolism
Animals
Chromatography
Dyneins - metabolism
Flagella
Hydrolysis
Kinetics
Male
Microtubules
Microtubules - enzymology
Molecules
Nucleotides
Nucleotides - metabolism
Sea Urchins - physiology
Sliding
Sperm Tail - physiology
Spermatozoa
Spermatozoa - physiology
Structure-Activity Relationship
Vanadates
Vanadium - pharmacology
title Mechanochemical Coupling in the Relaxation of Rigor-Wave Sea Urchin Sperm Flagella
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