Effects of Macromolecular Crowding on Biochemical Systems

被引:29
作者
Silverstein, Todd P. [1 ]
Slade, Kristin [2 ]
机构
[1] Willamette Univ, Dept Chem, Salem, OR 97301 USA
[2] Hobart & William Smith Coll, Dept Chem, Geneva, NY 14456 USA
关键词
Upper-Division Undergraduate; Biochemistry; Physical Chemistry; Curriculum; Laboratory Instruction; Proteins/Peptides; Biophysical Chemistry; Enzymes; Thermodynamics; PROTEIN STABILITY; EXCLUDED-VOLUME; IN-VIVO; MONOSACCHARIDE MIXTURES; THERMODYNAMIC ACTIVITY; CATALYZED HYDROLYSIS; POLYETHYLENE-GLYCOL; ENZYME; KINETICS; WATER;
D O I
10.1021/acs.jchemed.9b00399
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Living cells are crowded. The presence of so many macromolecules packed into a confined environment affects the structure and function of biological components, and the kinetics and thermodynamics of biochemical reactions. In fact, crowding studies have already led to important biological insights, such as the existence of metabolons and other temporary protein complexes that play essential roles in metabolism, cell signaling, and organization of the intracellular environment. Even so, this important topic is rarely addressed in chemistry and biochemistry curricula. This review brings readers up to date on developments in the field of macromolecular crowding, with a special emphasis on distinguishing between the two major components of crowding: excluded volume effects (hard interactions) and chemical effects (soft interactions). Interestingly, because attractive soft interactions and repulsive hard interactions oppose each other, the net effects of crowding in vivo are often surprisingly. small. We present some background and theory, while summarizing recent literature. Finally, we include suggestions on how this topic might be incorporated into the biochemistry classroom or laboratory setting.
引用
收藏
页码:2476 / 2487
页数:23
相关论文
共 125 条
[1]   Large cosolutes, small cosolutes, and dihydrofolate reductase activity [J].
Acosta, Luis C. ;
Goncalves, Gerardo M. Perez ;
Pielak, Gary J. ;
Gorensek-Benitez, Annelise H. .
PROTEIN SCIENCE, 2017, 26 (12) :2417-2425
[3]   Cytosol-mimetic chemistry:: Kinetics of the trypsin-catalyzed hydrolysis of p-nitrophenyl acetate upon addition of polyethylene glycol and N-tert-butyl acetoacetamide [J].
Asaad, N ;
Engberts, JBFN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (23) :6874-6875
[4]   Assessment of Course-Based Undergraduate Research Experiences: A Meeting Report [J].
Auchincloss, Lisa Corwin ;
Laursen, Sandra L. ;
Branchaw, Janet L. ;
Eagan, Kevin ;
Graham, Mark ;
Hanauer, David I. ;
Lawrie, Gwendolyn ;
McLinn, Colleen M. ;
Pelaez, Nancy ;
Rowland, Susan ;
Towns, Marcy ;
Trautmann, Nancy M. ;
Varma-Nelson, Pratibha ;
Weston, Timothy J. ;
Dolan, Erin L. .
CBE-LIFE SCIENCES EDUCATION, 2014, 13 (01) :29-40
[5]   A Comprehensive Enzyme Kinetic Exercise for Biochemistry [J].
Barton, Janice S. .
JOURNAL OF CHEMICAL EDUCATION, 2011, 88 (09) :1336-1339
[6]   Impact of protein denaturants and stabilizers on water structure [J].
Batchelor, JD ;
Olteanu, A ;
Tripathy, A ;
Pielak, GJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (07) :1958-1961
[7]   Nonadditive effects of mixed crowding on protein stability [J].
Batra, Jyotica ;
Xu, Ke ;
Zhou, Huan-Xiang .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2009, 77 (01) :133-138
[8]   Comparison of the thermal stabilization of proteins by oligosaccharides and monosaccharide mixtures: Measurement and analysis in the context of excluded volume theory [J].
Beg, Ilyas ;
Minton, Allen P. ;
Islam, Asimul ;
Hassan, Md Imtaiyaz ;
Ahmad, Faizan .
BIOPHYSICAL CHEMISTRY, 2018, 237 :31-37
[9]   Making microenvironments: A look into incorporating macromolecular crowding into in vitro experiments, to generate biomimetic microenvironments which are capable of directing cell function for tissue engineering applications [J].
Benny, Paula ;
Raghunath, Michael .
JOURNAL OF TISSUE ENGINEERING, 2017, 8
[10]   Unexpected Effects of Macromolecular Crowding on Protein Stability [J].
Benton, Laura A. ;
Smith, Austin E. ;
Young, Gregory B. ;
Pielak, Gary J. .
BIOCHEMISTRY, 2012, 51 (49) :9773-9775