Annual review of biophysics and biomolecular structure最新文献

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Conformational spread: the propagation of allosteric states in large multiprotein complexes. 构象扩散:大型多蛋白复合物中变构状态的传播。
Annual review of biophysics and biomolecular structure Pub Date : 2004-01-01 DOI: 10.1146/annurev.biophys.33.110502.132703
Dennis Bray, Thomas Duke
{"title":"Conformational spread: the propagation of allosteric states in large multiprotein complexes.","authors":"Dennis Bray,&nbsp;Thomas Duke","doi":"10.1146/annurev.biophys.33.110502.132703","DOIUrl":"https://doi.org/10.1146/annurev.biophys.33.110502.132703","url":null,"abstract":"<p><p>The phenomenon of allostery is conventionally described for small symmetrical oligomeric proteins such as hemoglobin. Here we review experimental evidence from a variety of systems-including bacterial chemotaxis receptors, muscle ryanodine receptors, and actin filaments-showing that conformational changes can also propagate through extended lattices of protein molecules. We explore the statistical mechanics of idealized linear and two-dimensional arrays of allosteric proteins and show that, as in the analogous Ising models, arrays of closely packed units can show large-scale integrated behavior. We also discuss proteins that undergo conformational changes driven by the hydrolysis of ATP and give examples in which these changes propagate through linear chains of molecules. We suggest that conformational spread could provide the basis of a solid-state \"circuitry\" in a living cell, able to integrate biochemical and biophysical events over hundreds of protein molecules.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"33 ","pages":"53-73"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.33.110502.132703","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"24515919","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 193
Computer simulations of enzyme catalysis: methods, progress, and insights. 酶催化的计算机模拟:方法、进展和见解。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-02-05 DOI: 10.1146/annurev.biophys.32.110601.141807
Arieh Warshel
{"title":"Computer simulations of enzyme catalysis: methods, progress, and insights.","authors":"Arieh Warshel","doi":"10.1146/annurev.biophys.32.110601.141807","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.141807","url":null,"abstract":"<p><p>Understanding the action of enzymes on an atomistic level is one of the important aims of modern biophysics. This review describes the state of the art in addressing this challenge by simulating enzymatic reactions. It considers different modeling methods including the empirical valence bond (EVB) and more standard molecular orbital quantum mechanics/molecular mechanics (QM/MM) methods. The importance of proper configurational averaging of QM/MM energies is emphasized, pointing out that at present such averages are performed most effectively by the EVB method. It is clarified that all properly conducted simulation studies have identified electrostatic preorganization effects as the source of enzyme catalysis. It is argued that the ability to simulate enzymatic reactions also provides the chance to examine the importance of nonelectrostatic contributions and the validity of the corresponding proposals. In fact, simulation studies have indicated that prominent proposals such as desolvation, steric strain, near attack conformation, entropy traps, and coherent dynamics do not account for a major part of the catalytic power of enzymes. Finally, it is pointed out that although some of the issues are likely to remain controversial for some time, computer modeling approaches can provide a powerful tool for understanding enzyme catalysis.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"425-43"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.141807","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22234810","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 393
Structure and function of natural killer cell surface receptors. 自然杀伤细胞表面受体的结构与功能。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2002-12-02 DOI: 10.1146/annurev.biophys.32.110601.142347
Sergei Radaev, Peter D Sun
{"title":"Structure and function of natural killer cell surface receptors.","authors":"Sergei Radaev,&nbsp;Peter D Sun","doi":"10.1146/annurev.biophys.32.110601.142347","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.142347","url":null,"abstract":"<p><p>Since mid-1990, with cloning and identification of several families of natural killer (NK) receptors, research on NK cells began to receive appreciable attention. Determination of structures of NK cell surface receptors and their ligand complexes led to a fast growth in our understanding of the activation and ligand recognition by these receptors as well as their function in innate immunity. Functionally, NK cell surface receptors are divided into two groups, the inhibitory and the activating receptors. Structurally, they belong to either the immunoglobulin (Ig)-like receptor superfamily or the C-type lectin-like receptor (CTLR) superfamily. Their ligands are either members of class I major histocompatibility complexes (MHC) or homologs of class I MHC molecules. The inhibitory form of NK receptors provides the protective immunity through recognizing class I MHC molecules with self-peptides on healthy host cells. The activating, or the noninhibitory, NK receptors mediate the killing of tumor or virally infected cells through their specific ligand recognition. The structures of activating and inhibitory NK cell surface receptors and their complexes with the ligands determined to date, including killer immunoglobulin-like receptors (KIRs) and their complexes with HLA molecules, CD94, Ly49A, and its complex with H-2Dd, and NKG2D receptors and their complexes with class I MHC homologs, are reviewed here.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"93-114"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.142347","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22144598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 95
Liquid-liquid immiscibility in membranes. 膜中的液-液不混相。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-01-31 DOI: 10.1146/annurev.biophys.32.110601.141704
Harden M McConnell, Marija Vrljic
{"title":"Liquid-liquid immiscibility in membranes.","authors":"Harden M McConnell,&nbsp;Marija Vrljic","doi":"10.1146/annurev.biophys.32.110601.141704","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.141704","url":null,"abstract":"<p><p>The observation of liquid-liquid immiscibility in cholesterol-phospholipid mixtures in monolayers and bilayers has opened a broad field of research into their physical chemistry. Some mixtures exhibit multiple immiscibilities. This unusual property has led to a thermodynamic model of \"condensed complexes.\" These complexes are the consequence of an exothermic, reversible reaction between cholesterol and phospholipids. In this quantitative model the complexes are sometimes concentrated in a separate liquid phase. The phase separation into a complex-rich phase depends on membrane composition and intensive variables such as temperature. The properties of defined cholesterol-phospholipid mixtures provide a conceptual foundation for the exploration of a number of aspects of the biophysics and biochemistry of animal cell membranes.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"469-92"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.141704","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22234809","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 241
The structure of mammalian cyclooxygenases. 哺乳动物环氧合酶的结构。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-02-05 DOI: 10.1146/annurev.biophys.32.110601.141906
R Michael Garavito, Anne M Mulichak
{"title":"The structure of mammalian cyclooxygenases.","authors":"R Michael Garavito,&nbsp;Anne M Mulichak","doi":"10.1146/annurev.biophys.32.110601.141906","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.141906","url":null,"abstract":"<p><p>Cyclooxygenases-1 and -2 (COX-1 and COX-2, also known as prostaglandin H2 synthases-1 and -2) catalyze the committed step in prostaglandin synthesis. COX-1 and -2 are of particular interest because they are the major targets of nonsteroidal antiinflammatory drugs (NSAIDs) including aspirin, ibuprofen, and the new COX-2-selective inhibitors. Inhibition of the COXs with NSAIDs acutely reduces inflammation, pain, and fever, and long-term use of these drugs reduces the incidence of fatal thrombotic events, as well as the development of colon cancer and Alzheimer's disease. In this review, we examine how the structures of COXs relate mechanistically to cyclooxygenase and peroxidase catalysis and how alternative fatty acid substrates bind within the COX active site. We further examine how NSAIDs interact with COXs and how differences in the structure of COX-2 result in enhanced selectivity toward COX-2 inhibitors.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"183-206"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.141906","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22234812","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 136
Optical single transporter recording: transport kinetics in microarrays of membrane patches. 光学单转运体记录:膜贴片微阵列中的转运动力学。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-02-06 DOI: 10.1146/annurev.biophys.32.110601.142429
Reiner Peters
{"title":"Optical single transporter recording: transport kinetics in microarrays of membrane patches.","authors":"Reiner Peters","doi":"10.1146/annurev.biophys.32.110601.142429","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.142429","url":null,"abstract":"<p><p>Optical single transporter recording (OSTR) is an emerging technique for the fluorescence microscopic measurement of transport kinetics in membrane patches. Membranes are attached to transparent microarrays of cylindrical test compartments (TCs) approximately 0.1-100 mum in diameter and approximately 10-100 mum in depth. Transport across membrane patches that may contain single transporters or transporter populations is recorded by confocal microscopy. By these means transport of proteins through single nuclear pore complexes has been recorded at rates of <1 translocation/s. In addition to the high sensitivity in terms of measurable transport rates OSTR features unprecedented spatial selectivity and parallel processing. This article reviews the conceptual basis of OSTR and its realization. Applications to nuclear transport are summarized. The further development of OSTR is discussed and its extension to a diversity of transporters, including translocases and ATP-binding cassette (ABC) pumps, projected.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"47-67"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.142429","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22234813","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 39
The crystallographic model of rhodopsin and its use in studies of other G protein-coupled receptors. 视紫红质的晶体学模型及其在其他G蛋白偶联受体研究中的应用。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-02-05 DOI: 10.1146/annurev.biophys.32.110601.142520
Slawomir Filipek, David C Teller, Krzysztof Palczewski, Ronald Stenkamp
{"title":"The crystallographic model of rhodopsin and its use in studies of other G protein-coupled receptors.","authors":"Slawomir Filipek,&nbsp;David C Teller,&nbsp;Krzysztof Palczewski,&nbsp;Ronald Stenkamp","doi":"10.1146/annurev.biophys.32.110601.142520","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.142520","url":null,"abstract":"<p><p>G protein-coupled receptors (GPCRs) are integral membrane proteins that respond to environmental signals and initiate signal transduction pathways activating cellular processes. Rhodopsin is a GPCR found in rod cells in retina where it functions as a photopigment. Its molecular structure is known from cryo-electron microscopic and X-ray crystallographic studies, and this has reshaped many structure/function questions important in vision science. In addition, this first GPCR structure has provided a structural template for studies of other GPCRs, including many known drug targets. After presenting an overview of the major structural elements of rhodopsin, recent literature covering the use of the rhodopsin structure in analyzing other GPCRs will be summarized. Use of the rhodopsin structural model to understand the structure and function of other GPCRs provides strong evidence validating the structural model.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"375-97"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.142520","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22234816","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 129
The state of lipid rafts: from model membranes to cells. 脂筏的状态:从模型膜到细胞。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-01-16 DOI: 10.1146/annurev.biophys.32.110601.142439
Michael Edidin
{"title":"The state of lipid rafts: from model membranes to cells.","authors":"Michael Edidin","doi":"10.1146/annurev.biophys.32.110601.142439","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.142439","url":null,"abstract":"<p><p>Lipid raft microdomains were conceived as part of a mechanism for the intracellular trafficking of lipids and lipid-anchored proteins. The raft hypothesis is based on the behavior of defined lipid mixtures in liposomes and other model membranes. Experiments in these well-characterized systems led to operational definitions for lipid rafts in cell membranes. These definitions, detergent solubility to define components of rafts, and sensitivity to cholesterol deprivation to define raft functions implicated sphingolipid- and cholesterol-rich lipid rafts in many cell functions. Despite extensive work, the basis for raft formation in cell membranes and the size of rafts and their stability are all uncertain. Recent work converges on very small rafts <10 nm in diameter that may enlarge and stabilize when their constituents are cross-linked.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"257-83"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.142439","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22209767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1288
Structure and function of the calcium pump. 钙泵的结构和功能。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-02-19 DOI: 10.1146/annurev.biophys.32.110601.142433
David L Stokes, N Michael Green
{"title":"Structure and function of the calcium pump.","authors":"David L Stokes,&nbsp;N Michael Green","doi":"10.1146/annurev.biophys.32.110601.142433","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.142433","url":null,"abstract":"<p><p>Active transport of cations is achieved by a large family of ATP-dependent ion pumps, known as P-type ATPases. Various members of this family have been targets of structural and functional investigations for over four decades. Recently, atomic structures have been determined for Ca2+-ATPase by X-ray crystallography, which not only reveal the architecture of these molecules but also offer the opportunity to understand the structural mechanisms by which the energy of ATP is coupled to calcium transport across the membrane. This energy coupling is accomplished by large-scale conformational changes. The transmembrane domain undergoes plastic deformations under the influence of calcium binding at the transport site. Cytoplasmic domains undergo dramatic rigid-body movements that deliver substrates to the catalytic site and that establish new domain interfaces. By comparing various structures and correlating functional data, we can now begin to associate the chemical changes constituting the reaction cycle with structural changes in these domains.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"445-68"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.142433","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22256653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 87
Acetylcholine binding protein (AChBP): a secreted glial protein that provides a high-resolution model for the extracellular domain of pentameric ligand-gated ion channels. 乙酰胆碱结合蛋白(Acetylcholine binding protein, AChBP):一种分泌性胶质蛋白,为五聚体配体门控离子通道的胞外结构域提供了高分辨率模型。
Annual review of biophysics and biomolecular structure Pub Date : 2003-01-01 Epub Date: 2003-02-21 DOI: 10.1146/annurev.biophys.32.110601.142536
Titia K Sixma, August B Smit
{"title":"Acetylcholine binding protein (AChBP): a secreted glial protein that provides a high-resolution model for the extracellular domain of pentameric ligand-gated ion channels.","authors":"Titia K Sixma,&nbsp;August B Smit","doi":"10.1146/annurev.biophys.32.110601.142536","DOIUrl":"https://doi.org/10.1146/annurev.biophys.32.110601.142536","url":null,"abstract":"<p><p>Acetylcholine binding protein (AChBP) has recently been identified from molluskan glial cells. Glial cells secrete it into cholinergic synapses, where it plays a role in modulating synaptic transmission. This novel mechanism resembles glia-dependent modulation of glutamate synapses, with several key differences. AChBP is a homolog of the ligand binding domain of the pentameric ligand-gated ion-channels. The crystal structure of AChBP provides the first high-resolution structure for this family of Cys-loop receptors. Nicotinic acetylcholine receptors and related ion-channels such as GABAA, serotonin 5HT3, and glycine can be interpreted in the light of the 2.7 A AChBP structure. The structural template provides critical details of the binding site and helps create models for toxin binding, mutational effects, and molecular gating.</p>","PeriodicalId":8270,"journal":{"name":"Annual review of biophysics and biomolecular structure","volume":"32 ","pages":"311-34"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.biophys.32.110601.142536","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22341442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 144
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