/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 14 In the case of the bacterial sod... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

In the case of the bacterial sodium/leucine transporter, what is the key distinguishing feature about the bound sodium ions that ensures that other ions, particularly \(\mathrm{K}^{+},\) do not bind?

Short Answer

Expert verified
The key feature is the specific size and coordination environment that fits Na+ but not K+.

Step by step solution

01

Identify the role of Sodium and Other Ions

Understand that sodium ions ( Na^+ ) play a crucial role in the binding and transport mechanism of the bacterial sodium/leucine transporter. In contrast, potassium ions ( K^+ ) must be prevented from binding in order to maintain selective transport.
02

Examine Ion Selectivity Mechanism

Review the structural features of the transporter that might contribute to its selectivity. Ion channels often use size, charge, and specific atomic interactions as the basis for selectivity.
03

Analyze the Size Discrimination

Recognize that the selectivity filter of the transporter is usually tailored to fit sodium ions ( Na^+ ), which are smaller than potassium ions ( K^+ ). This size difference is one key feature that prevents K^+ from effectively binding.
04

Consider Charge Density and Coordination

Consider the importance of charge density and liganding sites within the transporter. Sodium ( Na^+ ) and potassium ( K^+ ) have different charge densities due to their differing sizes, influencing how they interact with the transporter. Often, the coordination environment is specific to Na^+ .
05

Summarize the Key Distinguishing Feature

Conclude that the primary distinguishing feature is the specific size and coordination environment that fits Na^+ but not K^+ , ensuring that the transporter selectively binds sodium ions.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91Ó°ÊÓ!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Ion Selectivity
Ion selectivity is a fundamental process in the transporters responsible for moving specific ions across biological membranes. In the case of the bacterial sodium/leucine transporter, ion selectivity plays an essential role in ensuring that only sodium ions (\( \text{Na}^+ \)) are effectively transported while unwanted ions like potassium (\( \text{K}^+ \)) are excluded. Selectivity relies on a precise combination of factors such as size, charge, and the coordination sites of the ion-binding space.
This selectivity is crucial for maintaining cellular function and ion balance, as it ensures that only the correct ions are transported under physiological conditions. By utilizing these selective features, the transporter can maintain high specificity for sodium, preventing unwanted binding that could disrupt cellular processes.
Size Discrimination
Size discrimination plays a significant role in the selectivity of ion transporters. This method relies on the physical dimensions of the ions. Sodium ions (\( \text{Na}^+ \)) are smaller compared to potassium ions (\( \text{K}^+ \)).
The transporter has a selectivity filter, which is finely tuned to fit the smaller sodium ions precisely. This filter acts like a gatekeeper, ensuring only ions of certain size can pass. It prevents larger ions, such as potassium, from effectively binding to the transporter.
  • Sodium ion radius: approximately 1.02 Ã….
  • Potassium ion radius: approximately 1.38 Ã….
The fine-tuned fit for sodium means larger ions like potassium do not interact effectively, thus safeguarding the specificity of the ion transport process.
Charge Density
Charge density is another critical feature in the selectivity of the sodium/leucine transporter. An ion's charge density refers to its charge over a particular volume. Because sodium ions (\( \text{Na}^+ \)) are smaller than potassium ions (\( \text{K}^+ \)), they have a higher charge density.
This increased charge density allows sodium to create stronger electrostatic interactions with the coordination sites within the transporter, favoring its binding. Potassium, having a lower charge density due to its larger size, cannot form these interactions as effectively.This variance in charge density is an important component in the selective process because the transporter is more aligned to interact robustly with ions having higher charge density, ensuring precise ion selection.
Coordination Environment
The coordination environment within an ion transporter is the specific arrangement of ligands that surround and interact with an ion at the binding site. For the bacterial sodium/leucine transporter, the coordination environment is designed to precisely fit and stabilize sodium ions (\( \text{Na}^+ \)).
This specificity results from the direct interactions between sodium ions and their liganding atoms, which provide a snug fit that maximizes binding efficiency. The ligands are arranged to perfectly complement the ionic charges and size of sodium, while potassium ions (\( \text{K}^+ \)), due to their different size and charge properties, find less favorable or no coordination, preventing them from binding effectively.
  • Binding sites are tailored for specific ions.
  • Sodium aligns well with the available ligand geometry.
This careful tailoring of the coordination environment ensures that only sodium ions can bind snugly, making the transport highly selective and efficient.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Certain proton pump inhibitors inhibit secretion of stomach acid and are among the most widely sold drugs in the world today. What pump does this type of drug inhibit, and where is this pump located?

An \(\mathrm{H}^{+}\) ion is smaller than an \(\mathrm{H}_{2} \mathrm{O}\) molecule, and a glycerol molecule, a three-carbon alcohol, is much larger. Both readily dissolve in \(\mathrm{H}_{2} \mathrm{O}\). Why do aquaporins fail to transport \(\mathrm{H}^{+}\) whereas some can transport glycerol?

Name the three classes of transporters. Explain which one or more of these classes is able to move glucose and which move bicarbonate \(\left(\mathrm{HCO}_{3}^{-}\right)\) against an electrochemical gradient. In the case of bicarbonate, but not glucose, the \(\Delta G\) of the transport process has two terms. What are these two terms, and why does the second not apply to glucose? Why are cotransporters often referred to as examples of secondary active transport?

Patch clamping can be used to measure the conductance properties of individual ion channels. Describe how patch clamping can be used to determine whether or not the gene coding for a putative \(K^{+}\) channel actually codes for a \(K^{+}\) or \(\mathrm{Na}^{+}\) channel.

GLUT 1 , found in the plasma membrane of erythrocytes, is a classic example of a uniporter. a. Design a set of experiments to prove that GLUT1 is indeed a glucose- specific uniporter rather than a galactoseor mannose-specific uniporter. b. Glucose is a 6 -carbon sugar while ribose is a 5 -carbon sugar. Despite this smaller size, ribose is not efficiently transported by GLUT \(1 .\) How can this be explained? c. \(A\) drop in blood sugar from 5 m \(M\) to 2.8 m \(M\) or below can cause confusion and fainting. Calculate the effect of this drop on glucose transport into cells expressing GLUT 1 d. How do liver and muscle cells maximize glucose uptake without changing \(V_{\max } ?\) e. Tumor cells expressing GLUT1 often have a higher \(V_{\max }\) for glucose transport than do normal cells of the same type. How could these cells increase the \(V_{\max }\) ? f. Fat and muscle cells modulate the \(V_{\max }\) for glucose uptake in response to insulin signaling. How?

See all solutions

Recommended explanations on Biology Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.